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Search Results (3,248)

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Keywords = Li ion

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18 pages, 3809 KiB  
Article
Electrochemical Impedance Spectroscopy Investigation on the Charge–Discharge Cycle Life Performance of Lithium-Ion Batteries
by Olivia Bruj and Adrian Calborean
Energies 2025, 18(6), 1324; https://doi.org/10.3390/en18061324 (registering DOI) - 7 Mar 2025
Abstract
In this work, we employed an electrochemical impedance spectroscopy analysis of commercial Li-ion Panasonic NCR18650B cells in order to monitor their cycle life performance and the influence of the C-rate on the charge/discharge processes. By applying a fast charge rate of 1.5 C, [...] Read more.
In this work, we employed an electrochemical impedance spectroscopy analysis of commercial Li-ion Panasonic NCR18650B cells in order to monitor their cycle life performance and the influence of the C-rate on the charge/discharge processes. By applying a fast charge rate of 1.5 C, we investigated their speed degradation within three distinct discharge rates, namely, 0.5 C, 1 C, and 1.5 C. In our first approach, we assessed the dynamics of the lithium-ion transport processes, as well as their dependence on discharge rates, with the aim of understanding how their performance correlates with usage conditions. We observed that, as the discharge current increases while the number of cycles decreases, the ohmic resistance in the aged state reduces. Moreover, the charge transfer resistance is not affected by the discharge current, as the values are inversely proportional to the current rate, but mostly by the number of cycles. By performing a state of health analysis of Li-ion batteries with different C-rates until they were completely discharged, we offer a clear indication of how much of the battery’s lifetime available energy was consumed and how much was left, anticipating further issues or when the battery needed replacing. Starting at 60% state of health, the battery degradation has a steeper increase at 0.5 C and 1 C, respectively, while for a deep 1.5 C discharge, it only increases when the battery charge rate can no longer be sustained. Finally, the resonance frequency results highlight a fast increase toward the end of life for 0.5 C and 1 C, which is directly correlated with the above results, as a potentiostatic electrochemical impedance spectroscopy sequence was applied every fourth charge/discharge cycle. When applied at 1.5 C, the linear trend is much more pronounced, similar to the state of health results. Full article
(This article belongs to the Special Issue Innovations and Challenges in New Battery Generations)
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<p>The equivalent Randles circuit (top); Nyquist plot for Li-ion cells (middle); Divided half-battery, describing the internal reactions allocated to each domain (bottom).</p>
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<p>Aging protocol used for Li-ion batteries.</p>
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<p><b>Left</b>—Nyquist plots in charge state, <b>Right</b>—Nyquist plots in discharge state.</p>
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<p>Comparison of the measured data for new and deteriorated lithium-ion batteries with a Nyquist plot.</p>
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<p>The dependence of SoH vs. cycle number for Batt.1, Batt.2, and Batt.3.</p>
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<p>The efficiency of the LIB cells.</p>
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<p>Data acquisition of Batt.1—resonance frequency in cycle 1.</p>
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<p>Resonance frequency with the spline fitting for charge–discharge rates of 0.5 C, 1 C, and 1.5 C.</p>
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<p>Voltage characteristic for the first and last cycle of Batt.3 (1.5 C discharging).</p>
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15 pages, 2959 KiB  
Article
Machine Learning-Assisted Design of Doping Strategies for High-Voltage LiCoO2: A Data-Driven Approach
by Man Fang, Yutong Yao, Chao Pang, Xiehang Chen, Yutao Wei, Fan Zhou, Xiaokun Zhang and Yong Xiang
Batteries 2025, 11(3), 100; https://doi.org/10.3390/batteries11030100 (registering DOI) - 7 Mar 2025
Abstract
Doping lithium cobalt oxide (LiCoO2) cathode materials is an effective strategy for mitigating the detrimental phase transitions that occur at high voltages. A deep understanding of the relationships between cycle capacity and the design elements of doped LiCoO2 is critical [...] Read more.
Doping lithium cobalt oxide (LiCoO2) cathode materials is an effective strategy for mitigating the detrimental phase transitions that occur at high voltages. A deep understanding of the relationships between cycle capacity and the design elements of doped LiCoO2 is critical for overcoming the existing research limitations. The key lies in constructing a robust and interpretable mapping model between data and performance. In this study, we analyze the correlations between the features and cycle capacity of 158 different element-doped LiCoO2 systems by using five advanced machine learning algorithms. First, we conducted a feature election to reduce model overfitting through a combined approach of mechanistic analysis and Pearson correlation analysis. Second, the experimental results revealed that RF and XGBoost are the two best-performing models for data fitting. Specifically, the RF and XGBoost models have the highest fitting performance for IC and EC prediction, with R2 values of 0.8882 and 0.8318, respectively. Experiments focusing on ion electronegativity design verified the effectiveness of the optimal combined model. We demonstrate the benefits of machine learning models in uncovering the core elements of complex doped LiCoO2 formulation design. Furthermore, these combined models can be employed to search for materials with superior electrochemical performance and processing conditions. In the future, we aim to develop more accurate and efficient machine learning algorithms to explore the microscopic mechanisms affecting doped layered oxide cathode material design, thereby establishing new paradigms for the research of high-performance cathode materials for lithium batteries. Full article
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<p>The flow chart of this research.</p>
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<p>Results histogram of Pearson coefficient correlations for every pair of variables in the data set.</p>
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<p>The feature importance plots of the selected nine features of the doped elements. We used the best-performing RF model for 1DC (<b>a</b>) and the best-performing XGBoost model for 25DC (<b>b</b>) predictions on the test set. The order of the <span class="html-italic">y</span>-axis labels indicates the importance of varied features. The <span class="html-italic">x</span>-axis shows the SHAP values, reflecting their contributions to the prediction model.</p>
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<p>(<b>a</b>–<b>c</b>) SEM images of (<b>a</b>) PLCO, (<b>b</b>) La–LCO, and (<b>c</b>) Bi–LCO. Insets in (<b>b</b>,<b>c</b>) are the EDS mappings of cross-section fabricated by FIB. (<b>d</b>) XRD patterns of PLCO, La–LCO, and Bi–LCO. (<b>e</b>) Enlarged view of (003) peaks derived from PLCO, La–LCO, and Bi–LCO. (<b>f</b>) Enlarged view of (104) peaks in the XRD patterns of cycled PLCO, La–LCO, and Bi–LCO.</p>
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<p>(<b>a</b>) XPS spectra of PLCO, Bi–LCO, and La–LCO before cycling. (<b>b</b>) XPS spectra of PLCO, Bi–LCO, and La–LCO after cycling. (<b>c</b>) The morphologies of the cycled 0.1% Bi–LCO. (<b>d</b>) The morphologies of the cycled 0.1% La–LCO.</p>
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<p>(<b>a</b>) Cycling performance of PLCO, 0.1%La–LCO, and 0.1%Bi–LCO. (<b>b</b>) Rate performance of PLCO, 0.1%La–LCO, and 0.1%Bi–LCO. (<b>c</b>) The dQ–dV curves of PLCO, 0.1%La–LCO, and 0.1%Bi–LCO at the first cycle. (<b>d</b>) Nyquist plots of the electrochemical impedance spectra measured at room temperature, and the equivalent circuit applied for data fit. (<b>e</b>) <span class="html-italic">Z</span>′ plotted against <span class="html-italic">w</span><sup>−1/2</sup> at the low-frequency region.</p>
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10 pages, 6059 KiB  
Article
Mg-Doped Li2FeTiO4 as a High-Performance Cathode Material Enabling Fast and Stable Li-ion Storage
by Pengqing Hou, Yingdong Qu, Rui Huang, Xinru Tian, Guanglong Li and Shaohua Luo
Inorganics 2025, 13(3), 76; https://doi.org/10.3390/inorganics13030076 - 6 Mar 2025
Viewed by 151
Abstract
As a multi-electron system material, the excellent capacity and environmentally benign properties of Li2FeTiO4 cathodes make them attractive for lithium-ion batteries. Nevertheless, their electrochemical performance has been hampered by poor conductivity and limited ion transport. In this work, the synthesis [...] Read more.
As a multi-electron system material, the excellent capacity and environmentally benign properties of Li2FeTiO4 cathodes make them attractive for lithium-ion batteries. Nevertheless, their electrochemical performance has been hampered by poor conductivity and limited ion transport. In this work, the synthesis of Mg-doped Li2MgxFe1−xTiO4 (LiFT-Mgx, x = 0, 0.01, 0.03, 0.05) cathode materials was successfully achieved. We observed significant gains in interlayer spacing, ionic conductivity, and kinetics. Hence, the sample of the LiFT-Mg0.03 cathode demonstrated charming initial capacity (112.1 mAh g−1, 0.05 C), stability (85.0%, 30 cycles), and rate capability (96.5 mAh g−1, 85.9%). This research provided precious insights into lithium storage with exceptional long-term stability and has the potential to drive the development of next-generation energy storage technologies. Full article
(This article belongs to the Special Issue Novel Research on Electrochemical Energy Storage Materials)
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<p>SEM images of: (<b>a</b>) LiFT; (<b>b</b>) LiFT-Mg0.01; (<b>c</b>) LiFT-Mg0.03; (<b>d</b>) LiFT-Mg0.05; (<b>e</b>) element mapping of LiFT-Mg0.03.</p>
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<p>(<b>a</b>) XRD images of different samples; (<b>b</b>) enlarged images of different samples.</p>
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<p>FTIR of LiFT-Mg0.03 at dry gel, pre-fired sample and the cathode material.</p>
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<p>TG-DSC of LiFT-Mg0.03 at dry gel.</p>
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<p>Normalized XAS spectra of: (<b>a</b>) Fe K-edge and (<b>b</b>) Ti K-edge of LiFT and LiFT-Mg0.03 samples.</p>
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<p>Charge/discharge curves of: (<b>a</b>) LiFT; (<b>b</b>) LiFT-Mg0.01; (<b>c</b>) LiFT-Mg0.03; and (<b>d</b>) LiFT-Mg0.05.</p>
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<p>(<b>a</b>) Cycle performance; (<b>b</b>) rate performance of LiFT, LiFT-Mg0.01, LiFT-Mg0.03, and LiFT-Mg0.05 samples; charge–discharge profiles of (<b>c</b>) LiFT and (<b>d</b>) LiFT-Mg0.03 samples at varied current densities.</p>
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<p>EIS of LiFT, LiFT-Mg0.01, LiFT-Mg0.03, and LiFT-Mg0.05 samples.</p>
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<p>(<b>a</b>) Cycle performance at 2.0 C; (<b>b</b>,<b>c</b>) SEM and XRD of LiFT-Mg0.03 after 200 cycles.</p>
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<p>CV curves of LiFT−Mg0.03 material.</p>
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13 pages, 6626 KiB  
Article
Exploring the Solubility of Ethylene Carbonate in Supercritical Carbon Dioxide: A Pathway for Sustainable Electrolyte Recycling from Li-Ion Batteries
by Nils Zachmann, Claude Cicconardi and Burçak Ebin
Batteries 2025, 11(3), 98; https://doi.org/10.3390/batteries11030098 - 4 Mar 2025
Viewed by 143
Abstract
Ethylene carbonate is, among other applications, used in Li-ion batteries as an electrolyte solvent to dissociate Li-salt. Supercritical CO2 extraction is a promising method for the recycling of electrolyte solvents from spent batteries. To design an extraction process, knowledge of the solute [...] Read more.
Ethylene carbonate is, among other applications, used in Li-ion batteries as an electrolyte solvent to dissociate Li-salt. Supercritical CO2 extraction is a promising method for the recycling of electrolyte solvents from spent batteries. To design an extraction process, knowledge of the solute solubility is essential. In this work, the solubility of ethylene carbonate at different pressure (80–160 bar) and temperature (40 °C, and 60 °C) conditions is studied. It is shown that the solubility of ethylene carbonate increased with pressure at both temperatures, ranging from 0.24 to 8.35 g/kg CO2. The retrieved solubility data were fitted using the Chrastil model, and the average equilibrium association number was determined to be 4.46 and 4.02 at 40 °C and 60 °C, respectively. Scanning electron microscopy, Fourier-transform infrared spectroscopy, and X-ray diffraction analysis of the collected ethylene carbonate indicated that the crystal morphology and structure remained unchanged. A proof-of-principle experiment showed that EC can be successfully extracted from Li-ion battery waste at 140 bar and 40 °C. Full article
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Graphical abstract

Graphical abstract
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<p>Schematic of the experimental set-up. (1) CO<sub>2</sub> tank, (2) syringe pump connected to a heating jacket, (3) on/off valve, (4), equilibrium chamber connected to a thermal couple and a pressure gauge, (5) metering valve, and (6) collection vials.</p>
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<p>Cumulative collected EC (g) plotted against the CO<sub>2</sub> of the different experimental runs (denoted as I, II, and III) at (<b>a</b>) 80 bar, (<b>b</b>) 100 bar, (<b>c</b>) 120 bar, (<b>d</b>) 140 bar, and (<b>e</b>) 160 bar and, isothermal conditions at 40 °C. The linear regression for the determination of the solubility is shown as a dashed line.</p>
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<p>Cumulative collected EC (g) plotted against the CO<sub>2</sub> of the different experimental runs (denoted as I, II, and III) at (<b>a</b>) 80 bar, (<b>b</b>) 100 bar, (<b>c</b>) 120 bar, (<b>d</b>) 140 bar, and (<b>e</b>) 160 bar and, isothermal conditions at 40 °C. The linear regression for the determination of the solubility is shown as a dashed line.</p>
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<p>Solubility of EC in scCO<sub>2</sub> at different pressure (80, 100, 120, 140 bar, and 160 bar) at isothermal temperature (40 °C and 60 °C) conditions. The uncertainty bars represent the standard error of the linear regression slope coefficient.</p>
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<p>Correlation between the experimental and correlated solubility data using the Chrastil model.</p>
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<p>FTIR spectra of the scCO<sub>2</sub> dissolved EC and initial EC between 4000 and 500 cm<sup>−1</sup>.</p>
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<p>XRD pattern of the scCO<sub>2</sub> dissolved EC and the initial EC at different pressures and temperatures in the 2Ɵ range from 10° to 55°. As a reference, the PDF card taken from EC is plotted.</p>
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<p>SEM images of the pristine EC with magnification at (<b>a</b>) 5000× and (<b>b</b>) 10,000×, as well as scCO<sub>2</sub> dissolved EC at 140 bar and 40 °C with magnification at (<b>c</b>) 5000× and (<b>d</b>) 10,000×.</p>
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<p>Extraction yield of EC from LiB black mass using two different extraction approaches. In the first approach, only 140 bar and 40 °C were used. In approach 2, the pressure was subsequently raised from 80 bar (Step 1) to 100 bar (Step 2) and then 140 bar (Step 3).</p>
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20 pages, 10436 KiB  
Article
FEM Study on Enhancing Crashworthiness of Cylindrical Li-Ion Battery Packs Using Spacers Between the Cells
by Adrian Daniel Muresanu and Mircea Cristian Dudescu
Appl. Sci. 2025, 15(5), 2720; https://doi.org/10.3390/app15052720 - 4 Mar 2025
Viewed by 164
Abstract
This study proposes a novel approach to improving the crashworthiness of lithium-ion cylindrical cell packs by strategically placing spacers between the cells. The spacers transform the initial line contacts into broader surface contacts, enhancing the overall stiffness of the pack and reducing radial [...] Read more.
This study proposes a novel approach to improving the crashworthiness of lithium-ion cylindrical cell packs by strategically placing spacers between the cells. The spacers transform the initial line contacts into broader surface contacts, enhancing the overall stiffness of the pack and reducing radial deformation during compression. The concept was evaluated using finite element analysis (FEA), leveraging established material models to efficiently assess the concept’s potential prior to physical testing. To validate the robustness of the homogenized cell material and its application in a full pack, a compression experiment was performed on a pack of nine cells. The experimental results aligned closely with the simulation data, underlining the reliability of the material model and simulation methodology. Across all configurations and load cases—quasi-static compression using a plate or cylinder, and dynamic impact tests simulating crash indentation with a ball—the inclusion of spacers resulted in significant reductions in cell deformation and pack intrusion. The study also examined three spacer materials: aluminum, printed PLA, and printed PLA conditioned at 60 °C. The results showed that stiffer spacers, such as those made of aluminum, were the most effective in improving crash performance. However, even the conditioned PLA spacer, despite its lower stiffness, delivered meaningful benefits by enhancing structural integrity and reducing deformation. This demonstrates the versatility of the spacer concept, which can accommodate a range of materials based on specific performance and manufacturing requirements. These findings establish a solid foundation for the practical implementation of spacers in electric vehicle battery packs. Future research should include experimental validation under real-world crash conditions and explore spacer design and material optimization to maximize crashworthiness without compromising energy density or thermal performance. Full article
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<p>Graphical representation of the concept.</p>
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<p>Cell packing configuration: (<b>a</b>) V1; (<b>b</b>) V2; (<b>c</b>) V3.</p>
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<p>Impactors used for compression: (<b>a</b>) compression plate; (<b>b</b>) compression cylinder.</p>
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<p>Spacers for different configurations tested in this paper: (<b>a</b>) V1; (<b>b</b>) V2; (<b>c</b>) V3.</p>
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<p>Cell pack compression experiment: (<b>a</b>) no spacers; (<b>b</b>) printed spacers.</p>
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<p>Compression force–displacement validation curves.</p>
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<p>Compression plate load–displacement curve for different cells configurations: (<b>a</b>) V1; (<b>b</b>) V2; (<b>c</b>) V3.</p>
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<p>Compression plate, cell configuration V1, center-cut deformation for different spacers material: (<b>a</b>) aluminum; (<b>b</b>) printed PLA; (<b>c</b>) printed PLA at 60 °C.</p>
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<p>Compression plate, cell configuration V2, center-cut deformation for different spacer’s material: (<b>a</b>) aluminum; (<b>b</b>) printed PLA; (<b>c</b>) printed PLA at 60 °C.</p>
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<p>Compression plate, cell configuration V3, center-cut deformation for different spacer’s material: (<b>a</b>) aluminum; (<b>b</b>) printed PLA; (<b>c</b>) printed PLA at 60 °C.</p>
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<p>Compression cylinder load–displacement curve for different cells configurations: (<b>a</b>) V1; (<b>b</b>) V2; (<b>c</b>) V3.</p>
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<p>Compression cylinder, cell configuration V1, center-cut deformation for different spacer materials: (<b>a</b>) aluminum; (<b>b</b>) printed PLA; (<b>c</b>) printed PLA at 60 °C.</p>
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<p>Compression cylinder, cell configuration V2, center-cut deformation for different spacer materials: (<b>a</b>) aluminum; (<b>b</b>) printed PLA; (<b>c</b>) printed PLA at 60 °C.</p>
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<p>Compression cylinder, cell configuration V3, center-cut deformation for different spacer materials: (<b>a</b>) aluminum; (<b>b</b>) printed PLA; (<b>c</b>) printed PLA at 60 °C.</p>
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<p>Dynamic loading intrusion in V1 cell configuration: (<b>a</b>) no spacers; (<b>b</b>) aluminum; (<b>c</b>) printed PLA; (<b>d</b>) printed PLA at 60 °C.</p>
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<p>Dynamic loading intrusion in V2 cell configuration: (<b>a</b>) no spacers; (<b>b</b>) aluminum; (<b>c</b>) printed PLA; (<b>d</b>) printed PLA at 60 °C.</p>
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<p>Dynamic loading intrusion in V3 cell configuration: (<b>a</b>) no spacers; (<b>b</b>) aluminum; (<b>c</b>) printed PLA; (<b>d</b>) printed PLA at 60 °C.</p>
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<p>Dynamic loading stress in V1 cell configuration at center cut: (<b>a</b>) no spacers; (<b>b</b>) aluminum; (<b>c</b>) printed PLA; (<b>d</b>) printed PLA at 60 °C.</p>
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<p>Dynamic loading stress in V2 cell configuration at center cut: (<b>a</b>) no spacers; (<b>b</b>) aluminum; (<b>c</b>) printed PLA; (<b>d</b>) printed PLA at 60 °C.</p>
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<p>Dynamic loading stress in V3 cell configuration at center cut: (<b>a</b>) no spacers; (<b>b</b>) aluminum; (<b>c</b>) printed PLA; (<b>d</b>) printed PLA at 60 °C.</p>
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16 pages, 9618 KiB  
Article
Copper Hexacyanoferrates Obtained via Flavocytochrome b2 Assistance: Characterization and Application
by Galina Gayda, Olha Demkiv, Nataliya Stasyuk, Halyna Klepach, Roman Serkiz, Faina Nakonechny, Mykhailo Gonchar and Marina Nisnevitch
Biosensors 2025, 15(3), 157; https://doi.org/10.3390/bios15030157 - 2 Mar 2025
Viewed by 202
Abstract
Artificial enzymes or nanozymes (NZs) are gaining significant attention in biotechnology due to their stability and cost-effectiveness. NZs can offer several advantages over natural enzymes, such as enhanced stability under harsh conditions, longer shelf life, and reduced production costs. The booming interest in [...] Read more.
Artificial enzymes or nanozymes (NZs) are gaining significant attention in biotechnology due to their stability and cost-effectiveness. NZs can offer several advantages over natural enzymes, such as enhanced stability under harsh conditions, longer shelf life, and reduced production costs. The booming interest in NZs is likely to continue as their potential applications expand. In our previous studies, we reported the “green” synthesis of copper hexacyanoferrate (gCuHCF) using the oxidoreductase flavocytochrome b2 (Fcb2). Organic–inorganic micro-nanoparticles were characterized in detail, including their structure, composition, catalytic activity, and electron-mediator properties. An SEM analysis revealed that gCuHCF possesses a flower-like structure well-suited for concentrating and stabilizing Fcb2. As an effective peroxidase (PO) mimic, gCuHCF has been successfully employed for H2O2 detection in amperometric sensors and in several oxidase-based biosensors. In the current study, we demonstrated the uniqueness of gCuHCF that lies in its multifunctionality, serving as a PO mimic, a chemosensor for ammonium ions, a biosensor for L-lactate, and exhibiting perovskite-like properties. This exceptional ability of gCuHCF to enhance fluorescence under blue light irradiation is being reported for the first time. Using gCuHCF as a PO-like NZ, novel oxidase-based sensors were developed, including an optical biosensor for L-arginine analysis and electrochemical biosensors for methanol and glycerol determination. Thus, gCuHCF, synthesized via Fcb2, presents a promising platform for the development of amperometric and optical biosensors, bioreactors, biofuel cells, solar cells, and other advanced devices. The innovative approach of utilizing biocatalysts for nanoparticle synthesis highlights a groundbreaking direction in materials science and biotechnology. Full article
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Figure 1
<p>Examples of visualization in the ABTS- and <span class="html-italic">o</span>-dianisidine-based assays: (<b>a</b>)—PO-like activity of the chCuHCF (1) and gCuHCF (2–5) samples with the following activities (U/mL): 1—1.38; 2—2.12; 3—1.98; 4—3.78; 5—2.44. The substrate for PO-like activity contains a constant H<sub>2</sub>O<sub>2</sub> concentration. (<b>b</b>)—The dependence of color intensity on increasing H<sub>2</sub>O<sub>2</sub> concentrations (1–5), compared to the control sample without H<sub>2</sub>O<sub>2</sub> (6).</p>
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<p>Optical spectra of gCuHCF solutions (<b>a</b>) at different concentrations (mg/mL): 0 (1), 0.25 (2), 0.5 (3), 1 (4), 2 (5), and the calibration graph for photometric gCuHCF determination (<b>b</b>).</p>
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<p>Dependence of the optical density of the reaction mixture on H<sub>2</sub>O<sub>2</sub> concentration (<b>a</b>,<b>b</b>) and kinetic data linearization using the Lineweaver–Burke method (<b>c</b>). The initial gCuHCF concentration is 4.2 mg/mL.</p>
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<p>Examples of calibration graphs in the ArgO/gCuHCF/<span class="html-italic">o</span>-DZ naked-eye method for Arg determination (<b>a</b>), and the linearization of kinetic data using the Lineweaver–Burke method (<b>b</b>). The reaction mixtures (<b>a</b>) contain increasing concentrations of Arg (mM): 0 (1), 2 (2), 5 (3), 10 (4), 25 (5), 50 (6), 75 (7), 100 (8), with ArgO (1 U/mL) and varying gCuHCF concentrations (mg/mL): 4 (A), 2 (B), and 1 (C).</p>
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<p>Characteristics of the AO/gCuHCF/GE as an ABS for methanol: The CV profiles as outputs on methanol addition (<b>a</b>) up to concentration (mM): 0 (1, black), 2.5 (2, red) and 5 (3, blue), and the dependence of the current response on increasing concentrations of the analyte for a wide range (<b>b</b>) and a linear range (<b>c</b>). The GE was modified with 20 mU of gCuHCF exhibiting PO-like activity and 200 mU of AO. Conditions: scan rate (for <b>a</b>) is 50 mV·s<sup>−1</sup> vs. Ag/AgCl (reference electrode), working potential (for <b>b</b>,<b>c</b>) is 150 mV; 50 mM phosphate buffer, pH 7.0, 20 °C.</p>
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<p>Characteristics of the GlycO/gCuHCF/GE as an ABS for glycerol: The CV profiles as outputs on glycerol addition (<b>a</b>) up to concentration (mM): 0 (black), 12 (red), and 24 (blue); and the dependence of the current response on increasing concentrations of the analyte in the wide (<b>b</b>) and linear (<b>c</b>) ranges. GE was modified with 20 mU of gCuHCF exhibiting PO-like activity and 150 mU of GlycO. Conditions: scan rate (for <b>a</b>) is 50 mV s<sup>−1</sup> vs. Ag/AgCl (reference electrode), working potential (for <b>b</b>,<b>c</b>) is 150 mV; 50 mM phosphate buffer, pH 8.0, 20 °C.</p>
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<p>CV profiles of fresh-prepared gCuHCF/GE as biosensor on lactate: outputs on substrate addition up to concentration (mM): 0 (<b>1</b>, black), 15 (<b>2</b>, red), 30 (<b>3</b>, green), and 50 (<b>4</b>, blue). Conditions: scan rate 50 mV·s<sup>−1</sup> vs. Ag/AgCl as reference electrode, 50 mM acetate buffer, pH 6.0, 20 °C. The sensing layer contains 4.1 mU Fc<span class="html-italic">b</span><sub>2</sub>.</p>
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<p>Characteristics of the gCuHCF/Ges as ABS-1 and ABS-2 for lactate: the dependence of the current response on increasing concentrations of the analyte is demonstrated in both wide (<b>a</b>,<b>d</b>) and linear ranges (<b>b</b>,<b>c</b>,<b>e</b>,<b>f</b>). ABSs contain different amounts of fresh gCuHCFs: 5 µL (<b>1</b>, black line) and 10 µL (<b>2</b>, red line). Measurements were performed in 50 mM acetate buffer, pH 6.0 (<b>a</b>–<b>c</b>), and in 50 mM phosphate buffer, pH 7.0 (<b>d</b>–<b>f</b>), working potential of +300 vs. Ag/AgCl (reference electrode), at 23 °C mV.</p>
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<p>Characteristics of gCuHCF/GE as a chemosensor for ammonium ions: CV profiles as outputs on ammonium chloride addition (<b>a</b>) up to concentration (mM): 0 (<b>1</b>, black), 30 (<b>2</b>, red), and 60 (<b>3</b>, blue); chronoamperogram (<b>b</b>), dependence of the amperometric response on increasing ammonium chloride concentrations (<b>c</b>–<b>f</b>) in wide (<b>c</b>,<b>e</b>) and linear ranges (<b>d</b>,<b>f</b>). Conditions: scan rate (for <b>a</b>) is 50 mV·s<sup>−1</sup> vs. Ag/AgCl (reference electrode); temperature: 23 °C. Working potentials: +150 mV (<b>b</b>,<b>c</b>,<b>d</b>) and −100 mV (<b>e</b>,<b>f</b>). Buffers: 50 mM sodium acetate, pH 4.5 (<b>b</b>–<b>d</b>) and 50 mM sodium phosphate, pH 8.0 (<b>e</b>,<b>f</b>).</p>
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<p>Microscopic characterization of freshly prepared gCuHCFs suspended in 50 mM phosphate buffer: SEM image (<b>a</b>) and fluorescence images (<b>b</b>–<b>f</b>) captured under different filters. The images include brightfield (<b>b</b>) and blue-light fluorescence (<b>c</b>–<b>f</b>), showing dynamic changes over 1 to 5 min after irradiation with a 100 ms exposure.</p>
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<p>Microscopic characterization of freshly prepared gCuHCFs suspended in 50 mM phosphate buffer: SEM image (<b>a</b>) and fluorescence images (<b>b</b>–<b>f</b>) captured under different filters. The images include brightfield (<b>b</b>) and blue-light fluorescence (<b>c</b>–<b>f</b>), showing dynamic changes over 1 to 5 min after irradiation with a 100 ms exposure.</p>
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<p>Microscopic characterization of gCuHCFs samples: SEM images (<b>a</b>,<b>e</b>) and fluorescence images (<b>b</b>–<b>d</b>,<b>f</b>–<b>h</b>) captured under different filters. The FM images include brightfield (<b>b</b>,<b>f</b>) and DAPI-stained fluorescence (<b>c</b>,<b>d</b>,<b>g</b>,<b>h</b>), showing dynamic changes over 1 to 5 min after irradiation with a 100 ms exposure. gCuHCF samples were kept for 1 month at 4 °C as a suspension in water (<b>a</b>–<b>d</b>) and as a lyophilized powder, which was suspended in water before characterization (<b>e</b>–<b>h</b>).</p>
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14 pages, 3657 KiB  
Article
PFKM-Mediated Glycolysis: A Pathway for ASIC1 to Enhance Cell Survival in the Acidic Microenvironment of Liver Cancer
by Xiaomin Wu, Boshi Wang, Yingjian Hou, Yipeng Fang, Yuan Jiang, Yuelei Song, Youyi Liu and Cheng Jin
Biomolecules 2025, 15(3), 356; https://doi.org/10.3390/biom15030356 - 1 Mar 2025
Viewed by 268
Abstract
The acidic tumor microenvironment plays a critical role in promoting liver cancer cell survival by enhancing glycolysis and adaptive mechanisms. Acid-sensing ion channel 1 (ASIC1) is a key regulator of pH sensing, but its role in liver cancer progression and underlying mechanisms remain [...] Read more.
The acidic tumor microenvironment plays a critical role in promoting liver cancer cell survival by enhancing glycolysis and adaptive mechanisms. Acid-sensing ion channel 1 (ASIC1) is a key regulator of pH sensing, but its role in liver cancer progression and underlying mechanisms remain unclear. In this study, we examined ASIC1 expression in clinical liver tumor tissues using immunohistochemistry and immunofluorescence, correlating it with tumor stages. HepG2 and Li-7 cells were cultured in tumor supernatant and acidic conditions to mimic the tumor microenvironment. Western blotting assessed the expression of ASIC1 and glycolysis-related enzymes, with siRNA transfections used to investigate ASIC1 and phosphofructokinase muscle-type (PFKM) in liver cancer cell survival. Our results showed that ASIC1 expression was significantly elevated in liver tumor tissues and correlated with tumor progression. Acidic conditions increased ASIC1 expression in both cell lines, enhancing cell survival, while knockdown of ASIC1 reduced viability and increased apoptosis, particularly under acidic conditions. Moreover, PFKM silencing reversed the survival advantage conferred by ASIC1, confirming PFKM as a critical downstream effector. Additionally, lactate dehydrogenase (LDH) and phosphofructokinase (PFK) activity assays showed no significant changes, suggesting other regulatory mechanisms may also be involved. These findings suggest that the ASIC1/PFKM pathway promotes liver cancer cell survival in acidic environments, representing a potential therapeutic target for disrupting tumor adaptation in liver malignancies. Full article
(This article belongs to the Section Molecular Medicine)
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<p>ASIC1 expression is upregulated in liver tumor tissues and correlates with tumor stage. (<b>A</b>) Immunofluorescence staining shows ASIC1 expression in HCC tumor tissues and adjacent non-tumor tissues. Representative images are presented at 200× and 100× magnification. (<b>B</b>) Quantification of ASIC1-positive cells in tumor and adjacent non-tumor tissues. (<b>C</b>–<b>E</b>) Immunohistochemical staining of ASIC1 in liver tumor tissues at different clinical stages (Stage I, Stage II, and Stage III), showing a progressive increase in ASIC1 expression with advancing tumor stage. Representative images and quantification of ASIC1 expression are presented. The graphs show the means ± SEM of at least three independent experiments, **** <span class="html-italic">p</span> &lt; 0.0001, *** <span class="html-italic">p</span> &lt; 0.001,* <span class="html-italic">p</span> &lt; 0.05.</p>
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<p>The tumor acidic microenvironment induces ASIC1 expression and promotes HepG2 cell survival. (<b>A</b>,<b>B</b>) Western blot analysis of ASIC1 expression in HepG2 cells cultured in tumor culture supernatant (TSN) and normal medium (Normal) at pH 7.4 and pH 6.5, showing upregulation of ASIC1 in acidic conditions. (<b>C</b>) CCK-8 assay demonstrates reduced HepG2 cell viability at pH 6.5 compared to pH 7.4, but cells in TSN maintain higher viability than those in normal medium. (<b>D</b>,<b>E</b>) CCK-8 assay shows higher cell viability in TSN at pH 6.0 compared to normal medium at pH 6.0. (<b>F</b>) Western blot confirms increased ASIC1 expression in TSN at pH 6.0 compared to normal medium. Data are expressed as the mean ± SEM from at least three independent experiments, *** <span class="html-italic">p</span> &lt; 0.001, ** <span class="html-italic">p</span> &lt; 0.01, * <span class="html-italic">p</span> &lt; 0.05. Original images of (<b>A</b>,<b>F</b>) can be found in <a href="#app1-biomolecules-15-00356" class="html-app">Supplementary Materials</a>.</p>
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<p>ASIC1 enhances cell survival in the acidic tumor microenvironment. (<b>A</b>,<b>B</b>) Western blot validation of ASIC1 overexpression and knockdown in HepG2 cells. (<b>C</b>,<b>D</b>) CCK-8 assay showing that ASIC1 overexpression increases HepG2 cell viability in both pH 6.0 normal medium and pH 6.0 TSN. (<b>E</b>) Silencing ASIC1 with siRNA significantly reduces HepG2 cell viability in pH 6.0 TSN. Data are shown as mean ± SEM, *** <span class="html-italic">p</span> &lt; 0.001, * <span class="html-italic">p</span> &lt; 0.05. In the statistical bar graphs, the orange bars represent the blank control group, the green bars represent the empty-vector control group, the red bars represent the ASIC1-overexpression group, and the purple bars represent the ASIC1-knockdown group. Original images of (<b>A</b>,<b>B</b>) can be found in <a href="#app1-biomolecules-15-00356" class="html-app">Supplementary Materials</a>.</p>
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<p>ASIC1 inhibits apoptosis in the acidic tumor microenvironment. (<b>A</b>,<b>B</b>) Flow cytometry analysis of apoptosis in HepG2 cells cultured in pH 6.0 normal medium and TSN. ASIC1 overexpression reduces apoptosis under acidic conditions. (<b>C</b>) Silencing ASIC1 significantly increases apoptosis in pH 6.0 TSN. Data are presented as mean ± SEM from at least three independent experiments, *** <span class="html-italic">p</span> &lt; 0.001, ** <span class="html-italic">p</span> &lt; 0.01. In the statistical bar graphs, the orange bars represent the blank control group, the green bars rep-resent the empty-vector control group, the red bars represent the ASIC1-overexpression group, and the purple bars represent the ASIC1-knockdown group.</p>
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<p>ASIC1 regulates PFKM expression in the acidic tumor microenvironment. (<b>A</b>) Correlation analysis using the TCGA database shows a positive correlation between ASIC1 expression and glycolysis-related enzymes, including hexokinase (HK2), phosphofructokinase (PFKM), and pyruvate kinase (PKM2). (<b>B</b>,<b>C</b>) Western blot analysis shows that overexpression of ASIC1 increases PFKM expression in both pH 6.5 normal medium and TSN. (<b>D</b>,<b>E</b>) Silencing ASIC1 with siRNA decreases PFKM levels under the same conditions. Data are expressed as mean ± SEM from three independent experiments, *** <span class="html-italic">p</span> &lt; 0.001, * <span class="html-italic">p</span> &lt; 0.05. Original images of (<b>B</b>–<b>E</b>) can be found in <a href="#app1-biomolecules-15-00356" class="html-app">Supplementary Materials</a>.</p>
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<p>The ASIC1/PFKM pathway mediates HepG2 cell survival in the tumor acidic microenvironment. (<b>A</b>) Western blot analysis of PFKM expression in HepG2 cells transfected with three different siRNAs (siPFKM-1, siPFKM-2, siPFKM-3) or negative control (siNC), confirming that siPFKM-3 achieves the most potent knockdown. (<b>B</b>) Western blot validation of co-transfection of an ASIC1 overexpression vector (pcDNA3.1-ASIC1) and siPFKM-3 in HepG2 cells grown in pH 6.5 TSN. (<b>C</b>,<b>D</b>) Flow cytometry analysis of apoptosis in HepG2 cells shows that knocking down PFKM reverses the increased cell viability conferred by ASIC1 overexpression in both pH 6.0 (<b>C</b>) and pH 6.5 TSN (<b>D</b>). Data are presented as mean ± SEM, *** <span class="html-italic">p</span> &lt; 0.001, ** <span class="html-italic">p</span> &lt; 0.01, * <span class="html-italic">p</span> &lt; 0.05. In the statistical bar graphs, the orange bars represent the empty-vector control group, the red bars represent the ASIC1-overexpression group, the green bars rep-resent the ASIC1-overexpression and siNC group, and the blue bars represent the ASIC1-overexpression and PFKM-knockdown group. Original images of (<b>A</b>,<b>B</b>) can be found in <a href="#app1-biomolecules-15-00356" class="html-app">Supplementary Materials</a>.</p>
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27 pages, 4985 KiB  
Review
Analysis of State-of-Charge Estimation Methods for Li-Ion Batteries Considering Wide Temperature Range
by Yu Miao, Yang Gao, Xinyue Liu, Yuan Liang and Lin Liu
Energies 2025, 18(5), 1188; https://doi.org/10.3390/en18051188 - 28 Feb 2025
Viewed by 183
Abstract
Lithium-ion batteries are the core energy storage technology for electric vehicles and energy storage systems. Accurate state-of-charge (SOC) estimation is critical for optimizing battery performance, ensuring safety, and predicting battery lifetime. However, SOC estimation faces significant challenges under extreme temperatures and complex operating [...] Read more.
Lithium-ion batteries are the core energy storage technology for electric vehicles and energy storage systems. Accurate state-of-charge (SOC) estimation is critical for optimizing battery performance, ensuring safety, and predicting battery lifetime. However, SOC estimation faces significant challenges under extreme temperatures and complex operating conditions. This review systematically examines the research progress on SOC estimation techniques over a wide temperature range, focusing on two mainstream approaches: model improvement and data-driven methods. The model improvement method enhances temperature adaptability through temperature compensation and dynamic parameter adjustment. Still, it has limitations in dealing with the nonlinear behavior of batteries and accuracy and real-time performance at extreme temperatures. In contrast, the data-driven method effectively copes with temperature fluctuations and complex operating conditions by extracting nonlinear relationships from historical data. However, it requires high-quality data and substantial computational resources. Future research should focus on developing high-precision, temperature-adaptive models and lightweight real-time algorithms. Additionally, exploring the deep coupling of physical models and data-driven methods with multi-source heterogeneous data fusion technology can further improve the accuracy and robustness of SOC estimation. These advancements will promote the safe and efficient application of lithium batteries in electric vehicles and energy storage systems. Full article
(This article belongs to the Special Issue Electrochemical Conversion and Energy Storage System)
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<p>Lithium battery hierarchy (<b>A</b>) and working principle (<b>B</b>).</p>
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<p>Variations in the estimated <span class="html-italic">R</span><sub>1</sub> (<b>a</b>) and <span class="html-italic">R</span><sub>2</sub> (<b>b</b>) parameters with temperature at 60% SOC [<a href="#B7-energies-18-01188" class="html-bibr">7</a>].</p>
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<p>Thermal runaway reaction process.</p>
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<p>Schematic diagram of improved equivalent circuit model SOC estimation.</p>
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<p>Flowchart of SOC estimation based on CFR algorithm integrated learning algorithm [<a href="#B57-energies-18-01188" class="html-bibr">57</a>].</p>
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<p>Bagging structure (<b>A</b>) and Boosting structure (<b>B</b>).</p>
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<p>Typical structure of CNN.</p>
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<p>Comparison of LSTM, CNN, and FNN errors [<a href="#B70-energies-18-01188" class="html-bibr">70</a>].</p>
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<p>DNN Workflow [<a href="#B79-energies-18-01188" class="html-bibr">79</a>].</p>
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<p>Transfer learning process for battery SOC estimation models [<a href="#B84-energies-18-01188" class="html-bibr">84</a>].</p>
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30 pages, 2480 KiB  
Review
High-Volume Battery Recycling: Technical Review of Challenges and Future Directions
by Sheikh Rehman, Maher Al-Greer, Adam S. Burn, Michael Short and Xinjun Cui
Batteries 2025, 11(3), 94; https://doi.org/10.3390/batteries11030094 - 28 Feb 2025
Viewed by 476
Abstract
The growing demand for lithium-ion batteries (LIBs), driven by their use in portable electronics and electric vehicles (EVs), has led to an increasing volume of spent batteries. Effective end-of-life (EoL) management is crucial to mitigate environmental risks and prevent depletion of valuable raw [...] Read more.
The growing demand for lithium-ion batteries (LIBs), driven by their use in portable electronics and electric vehicles (EVs), has led to an increasing volume of spent batteries. Effective end-of-life (EoL) management is crucial to mitigate environmental risks and prevent depletion of valuable raw materials like lithium (Li), cobalt (Co), nickel (Ni), and manganese (Mn). Sustainable, high-volume recycling and material recovery are key to establishing a circular economy in the battery industry. This paper investigates challenges and proposes innovative solutions for high-volume LIB recycling, focusing on automation for large-scale recycling. Key issues include managing variations in battery design, chemistry, and topology, as well as the availability of sustainable raw materials and low-carbon energy sources for the recycling process. The paper presents a comparative study of emerging recycling techniques, including EV battery sorting, dismantling, discharge, and material recovery. With the expected growth in battery volume by 2030 (1.4 million per year by 2040), automation will be essential for efficient waste processing. Understanding the underlying processes in battery recycling is crucial for enabling safe and effective recycling methods. Finally, the paper emphasizes the importance of sustainable LIB recycling in supporting the circular economy. Our proposals aim to overcome these challenges by advancing automation and improving material recovery techniques. Full article
(This article belongs to the Special Issue Lithium-Ion Battery Recycling)
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<p>Projected EV production in the UK and EV battery capacity in Global Market from 2020 to 2030.</p>
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<p>Schematic overview of possible recycling routes for LIBs.</p>
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<p>EV Battery Tracking, Classification, and Sorting Mechanisms.</p>
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<p>Challenges of different battery pack designs in EV battery recycling (use of cylindrical, prismatic, and pouch cells).</p>
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<p>Proposed flowchart of EV battery recycling.</p>
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<p>Cost and environmental impacts of producing 1 kg of NMC111 from virgin material and recycled using different methods [<a href="#B140-batteries-11-00094" class="html-bibr">140</a>].</p>
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17 pages, 2410 KiB  
Article
Effects of Different Safety Vent Bursting Pressures on Lithium-Ion Battery Thermal Runaway Process and Reaction Product Compositions
by Honggang Sun, Gang Li, Haoran Zhao, Yuchong Yang and Chunmiao Yuan
Energies 2025, 18(5), 1173; https://doi.org/10.3390/en18051173 - 27 Feb 2025
Viewed by 146
Abstract
With the accelerated application of lithium-ion batteries, the design and optimization of their safety features have become increasingly important. However, the mechanisms by which different safety vent bursting pressures affect thermal runaway and its product compositions remain unclear. This study comparatively investigates the [...] Read more.
With the accelerated application of lithium-ion batteries, the design and optimization of their safety features have become increasingly important. However, the mechanisms by which different safety vent bursting pressures affect thermal runaway and its product compositions remain unclear. This study comparatively investigates the effects of safety vent bursting pressures of 1 MPa, 2 MPa, and 3 MPa on thermal runaway characteristics and product compositions. The results indicate that, under these three conditions, the safety vent bursts at approximately 800 s, 1000 s, and 1300 s after heating begins, with gas volumes of 5.3 L, 6.1 L, and 6.5 L, respectively. Additionally, higher bursting pressures lead to increased H2 production during thermal runaway. The characterization of solid product compositions reveals that the aluminum current collector participates in internal thermal runaway reactions, resulting in substances such as LiAlO2 or metallic Al in the solid products under different bursting pressures. This study provides important references for improving existing battery safety standards and optimizing battery safety designs. It also provides insights and references for metal recovery from batteries and investigations into battery fires. Full article
(This article belongs to the Topic Battery Design and Management)
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<p>Battery sample and vent bursting threshold control system.</p>
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<p>Comparison of bursting pressure of different layers of aluminum foil and commercial battery safety vents.</p>
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<p>TR trigger and product collection test system.</p>
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<p>Thermal runaway response and gas temperature in the vessel under different safety vent bursting pressures.</p>
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<p>Thermal runaway pressure and gas output under different safety vent bursting pressure conditions in the test vessel.</p>
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<p>Vent gas composition for battery thermal runaway with different vent bursting pressures.</p>
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<p>TR fragments of batteries with different vent bursting pressures.</p>
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<p>XRD characterization of solid products of battery TR.</p>
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<p>SEM-EDS image of TR products of different vent bursting pressures.</p>
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<p>SEM-EDS image of TR products of different vent bursting pressures.</p>
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<p>Schematic diagram of the possible formation reactions of gas and solid products in a battery.</p>
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24 pages, 3564 KiB  
Review
High-Temperature Stability of LiFePO4/Carbon Lithium-Ion Batteries: Challenges and Strategies
by Guangyao Jin, Wanwei Zhao, Jianing Zhang, Wenyu Liang, Mingyang Chen and Rui Xu
Sustain. Chem. 2025, 6(1), 7; https://doi.org/10.3390/suschem6010007 - 27 Feb 2025
Viewed by 137
Abstract
Lithium-ion batteries that use lithium iron phosphate (LiFePO4) as the cathode material and carbon (graphite or MCMB) as the anode have gained significant attention due to their cost-effectiveness, low environmental impact, and strong safety profile. These advantages make them suitable for [...] Read more.
Lithium-ion batteries that use lithium iron phosphate (LiFePO4) as the cathode material and carbon (graphite or MCMB) as the anode have gained significant attention due to their cost-effectiveness, low environmental impact, and strong safety profile. These advantages make them suitable for a wide range of applications including electric vehicles, stationary energy storage, and backup power systems. However, their adoption is hindered by a critical challenge: capacity degradation at elevated temperatures. This review systematically summarizes the corresponding modification strategies including surface modification of the anode and cathode as well as modification of the electrolyte, separator, binder, and collector. We further discuss the control of the charge state, early warning prevention, control of thermal runaway, and the rational application of ML and DFT to enhance the LFP/C high temperature cycling stability. Finally, in light of the current research challenges, promising research directions are presented, aiming at enhancing their performance and stability in such harsh thermal environments. Full article
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<p>Crystal structures of LiFePO<sub>4</sub> and FePO<sub>4</sub>. During charging, LiFePO<sub>4</sub> changes to FePO<sub>4</sub> by delithiation. In the discharge process, a reversible transformation from FePO<sub>4</sub> to LiFePO<sub>4</sub> occurs by lithiation. The image was taken with permission [<a href="#B8-suschem-06-00007" class="html-bibr">8</a>].</p>
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<p>The structure of graphite. The image was taken with permission [<a href="#B19-suschem-06-00007" class="html-bibr">19</a>].</p>
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<p>The structures of MCMBs. The image was taken with permission [<a href="#B22-suschem-06-00007" class="html-bibr">22</a>].</p>
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<p>Schematic diagram of SEI degradation pattern on the graphite anode side of the LFP cell. The image was taken with permission [<a href="#B33-suschem-06-00007" class="html-bibr">33</a>].</p>
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<p>Schematic of LFP cathode iron dissolution. The image was taken with permission [<a href="#B42-suschem-06-00007" class="html-bibr">42</a>].</p>
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<p>Cycle performance of LiFePO<sub>4</sub>/MCMB cells with different metal coatings including Au, Cu, Fe, Co, Ni, and Ti on the MCMB electrode surface (<b>a</b>). All cells were cycled at 1 C charge/discharge rate at 55 °C in the voltage window of 2.5–4.0 V. The image was taken with permission [<a href="#B51-suschem-06-00007" class="html-bibr">51</a>]. Relationship between reversible capacity retention and cycle number for SMG/LiFePO<sub>4</sub> 18650 batteries containing different binders cycled at 55 °C (<b>b</b>). The image was taken with permission [<a href="#B54-suschem-06-00007" class="html-bibr">54</a>]. SEM micrographs of cycled graphitic anode containing PVDF binder after 1 cycle (<b>c</b>); SBR/CMC binder after 1 cycle (<b>d</b>). The image was taken with permission [<a href="#B54-suschem-06-00007" class="html-bibr">54</a>].</p>
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<p>LTO-LFP/C synthesis flowchart (<b>a</b>). The image was taken with permission [<a href="#B57-suschem-06-00007" class="html-bibr">57</a>]. The cycling and CE performance for SS-LFP/C, SP-LFP/C and 3 and 5 wt.% LTO coated SP-LFP/C composites at 1C/3C rate at 25 and 55 °C (<b>b</b>). The image was taken with permission [<a href="#B57-suschem-06-00007" class="html-bibr">57</a>]. Cycle performances of ① LiFePO<sub>4</sub>; ② LiFePO<sub>3.98</sub>S<sub>0.03</sub> at 50 °C and ③ LiFePO<sub>4</sub>; and ④ LiFePO<sub>3.98</sub>S<sub>0.03</sub> at 60 °C (<b>c</b>). The image was taken with permission [<a href="#B59-suschem-06-00007" class="html-bibr">59</a>].</p>
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<p>Comparison of the cycle life of LiFePO<sub>4</sub>/graphite full cells at 55 °C (<b>a</b>); SEM micrographs of the anodes in the cells without VC (<b>b</b>) and with VC (<b>c</b>) after 100 cycles at 55 °C. The image was taken with permission [<a href="#B68-suschem-06-00007" class="html-bibr">68</a>].</p>
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<p>EIS at different SOC values when charging, with 10 min rest time at 25 °C (<b>a</b>). The image was taken with permission [<a href="#B90-suschem-06-00007" class="html-bibr">90</a>]. Trend in the relative capacity of the cycle degradation tests at 50% DOD and C-rates of 1.0, 2.0, 4.0, and 8.0 C at 40 °C (<b>b</b>). The images were taken with permission [<a href="#B92-suschem-06-00007" class="html-bibr">92</a>].</p>
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<p>Chain reactions of LFP batteries during TR (<b>a</b>). The images were taken with permission [<a href="#B94-suschem-06-00007" class="html-bibr">94</a>]. The sequence and advantages of warning signal response (<b>b</b>).The images were taken with permission [<a href="#B94-suschem-06-00007" class="html-bibr">94</a>].</p>
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14 pages, 3994 KiB  
Article
Impregnation of Se2S6 into a Nitrogen- and Sulfur-Co-Doped Functional Metal Carbides and Nitrides for High-Performance Li-S Batteries
by Lu Chen, Zhongyuan Zheng, Shuo Meng, Wenwei Wu, Weicheng Zhou, Shanshan Yang, Kexuan Liao, Yuanhui Zuo and Ting He
Molecules 2025, 30(5), 1070; https://doi.org/10.3390/molecules30051070 - 26 Feb 2025
Viewed by 150
Abstract
In this study, nitrogen- and sulfur-co-doped MXene (NS-MXene) was developed as a high-performance cathode material for lithium–sulfur (Li-S) batteries. Heterocyclic Se2S6 molecules were successfully confined within the NS-MXene structure using a simple melt impregnation method. The resulting NS-MXene exhibited a [...] Read more.
In this study, nitrogen- and sulfur-co-doped MXene (NS-MXene) was developed as a high-performance cathode material for lithium–sulfur (Li-S) batteries. Heterocyclic Se2S6 molecules were successfully confined within the NS-MXene structure using a simple melt impregnation method. The resulting NS-MXene exhibited a unique wrinkled morphology with a stable structure which facilitated rapid ion transport and provided a physical barrier to mitigate the shuttle effect of polysulfide. The introduction of nitrogen and sulfur heteroatoms into the MXene structure not only shifted the Ti d-band center towards the Fermi level but also significantly polarizes the MXene, enhancing the conversion kinetics and ion diffusion capability while preventing the accumulation of Li2S6. Additionally, the incorporation of Se and S in Se2S6 improved the conductivity compared to S alone, resulting in reduced polarization and enhanced electrical properties. Consequently, NS-MXene/Se2S6 exhibited excellent cycling stability, high reversible capacity, and reliable performance at high current densities and under extreme conditions, such as high sulfur loading and low electrolyte-to-sulfur ratios. This work presents a simple and effective strategy for designing heteroatom-doped MXene materials, offering promising potential for the development of high-performance, long-lasting Li-S batteries for practical applications. Full article
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<p>Synthesis diagram of NS-MXene/Se<sub>2</sub>S<sub>6</sub> cathode material.</p>
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<p>SEM images of (<b>a</b>) MAX-phase Ti<sub>3</sub>AlC<sub>2</sub> (<b>b</b>) MXene (<b>c</b>) NS-MXene (<b>d</b>) NS-MXene/Se<sub>2</sub>S<sub>6</sub>.</p>
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<p>TEM and HRTEM images of (<b>a</b>,<b>b</b>) MXene, (<b>c</b>,<b>d</b>) NS-MXene, (<b>e</b>,<b>f</b>) NS-MXene/Se<sub>2</sub>S<sub>6</sub>.</p>
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<p>(<b>a</b>) XRD patterns of Ti<sub>3</sub>AlC<sub>2</sub> MAX-phase, MXene and NS-MXene samples. (<b>b</b>) FTIR spectrum of MXene and NS-MXene sample. Ti 2p spectrum of the (<b>c</b>) MXene and (<b>d</b>) NS-MXene composites.</p>
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<p>XRD patterns of Se<sub>2</sub>S<sub>6</sub>, NS-MXene/Se<sub>2</sub>S<sub>6</sub>, and NS-MXene samples.</p>
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<p>Schematic illustration of the MXene doped with (<b>a</b>) N,S atoms, (<b>b</b>) N atoms, (<b>c</b>) S atoms.</p>
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<p>CV curves of cells with NS-MXene/Se<sub>2</sub>S<sub>6</sub> as cathodes at a scan rate of 0.1 mV S<sup>−1</sup>.</p>
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<p>(<b>a</b>) The Nyquist plots, (<b>b</b>) cycle performance, and (<b>c</b>) rate performance of Se<sub>2</sub>S<sub>6</sub>, MXene/Se<sub>2</sub>S<sub>6</sub> and NS-MXene/Se<sub>2</sub>S<sub>6</sub> cathodes.</p>
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<p>Cycling performance of the NS-MXene/Se<sub>2</sub>S<sub>6</sub> for specific capacity and areal capacity.</p>
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21 pages, 8672 KiB  
Article
Joint Prediction of Li-Ion Battery Cycle Life and Knee Point Based on Early Charging Performance
by Xinru Cui, Jinlong Zhang, Di Zhang, Yanjun Wei and Hanhong Qi
Symmetry 2025, 17(3), 351; https://doi.org/10.3390/sym17030351 - 26 Feb 2025
Viewed by 270
Abstract
With the rapid development of lithium-ion batteries, predicting battery life is critical to the safe operation of devices such as electric ships, electric vehicles, and energy storage systems. Given the complexity of the internal aging mechanism of batteries, their aging process exhibits prominent [...] Read more.
With the rapid development of lithium-ion batteries, predicting battery life is critical to the safe operation of devices such as electric ships, electric vehicles, and energy storage systems. Given the complexity of the internal aging mechanism of batteries, their aging process exhibits prominent nonlinear characteristics. Knee point, as a distinctive sign of this nonlinear aging process, plays a crucial role in predicting the battery’s lifetime. In this paper, the cycle life and cycle to the knee point of the battery are firstly predicted using the time dimension and space dimension features of the early external characteristics of the battery, respectively. Then, to capture the aging characteristics of batteries more comprehensively, we innovatively propose a joint prediction method of battery cycle life and knee point. Knee point features are incorporated into the battery cycle life prediction model in this method to fully account for the nonlinear aging characteristics of batteries. The experimental validation results show that the TECAN model, which combines time series features and knee point information, performs well, with a root mean square error (RMSE) of 106 cycles and a mean absolute percentage error (MAPE) of only 12%. Full article
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<p>Efficient channel attention module framework.</p>
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<p>Architecture of the spatial feature extraction module ECA-MCCA.</p>
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<p>The architecture of the temporal feature extraction module TECAN.</p>
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<p>A stack of dilated causal convolutions with convolution kernel size k = 3 and dilation factors d = 1, 2, 5.</p>
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<p>CL distribution of LIBs.</p>
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<p>Charging V, I, and T of three batteries with different charging strategies. (<b>a</b>) Time–charge voltage; (<b>b</b>) Time–charge current; (<b>c</b>) Time–temperature; (<b>d</b>) Charging capacity–charge voltage; (<b>e</b>) Charging capacity–charge current; (<b>f</b>) Charging capacity–temperature.</p>
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<p>Battery cycling data of the dataset. (<b>a</b>) The capacity fade trajectories of the selected batteries; (<b>b</b>) The knee point identification based on the bisector model on a capacity fade trajectory of one cell; (<b>c</b>) CTK and EOL distribution of the batteries.</p>
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<p>CL prediction model with the addition of CTK prediction (<b>a</b>) MODEL1: ECA-MCCA model with CTK prediction; (<b>b</b>) MODEL2: TECAN model with CTK prediction.</p>
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<p>Comparison of results of TECAN, TECAN-ECA-MCCA, and ECA-MCCA models for different battery CL. (<b>a</b>) Comparison of root mean square errors; (<b>b</b>) Comparison of mean absolute percentage errors.</p>
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<p>Observed CTK and predicted CTK for the training and test sets. (<b>a</b>) TECAN model CTK prediction results; (<b>b</b>) TECAN-ECA-MCCA model CTK prediction results; (<b>c</b>) ECA-MCCA model CTK prediction results. The inset shows the APE distribution for the training and test data.</p>
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<p>Predictions of CTK using the TECAN model with some N. (<b>a</b>) Comparison of root-mean-square error; (<b>b</b>) Comparison of mean absolute percentage error.</p>
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<p>Observed CL and predicted CL for the train sets and test sets. (<b>a</b>) ECA-MCCA model CL prediction results; (<b>b</b>) TECAN model CL prediction results; (<b>c</b>) TECAN-ECA-MCCA model CL prediction results. The inset shows the APE distribution of the training and test data.</p>
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<p>Prediction results of CL using MODEL1 and MODEL2 with some N. (<b>a</b>) Comparison of <span class="html-italic">RMSE</span> of prediction results of MODEL1 on test set of 43 batteries; (<b>b</b>) Comparison of <span class="html-italic">MAPE</span> of prediction results of MODEL1 for the test set of 43 batteries; (<b>c</b>) Comparison of <span class="html-italic">RMSE</span> of prediction results of MODEL2 on test set of 43 batteries; (<b>d</b>) Comparison of <span class="html-italic">MAPE</span> of prediction results of MODEL2 for the test set of 43 batteries.</p>
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18 pages, 5862 KiB  
Article
Evaluation of Indoor Power Performance of Emerging Photovoltaic Technology for IoT Device Application
by Yerassyl Olzhabay, Ikenna Henry Idu, Muhammad Najwan Hamidi, Dahaman Ishak, Arjuna Marzuki, Annie Ng and Ikechi A. Ukaegbu
Energies 2025, 18(5), 1118; https://doi.org/10.3390/en18051118 - 25 Feb 2025
Viewed by 221
Abstract
The rapid rise in the power conversion efficiency (PCE) of perovskite solar cells (PSCs) has opened the door for diverse potential applications in powering indoor Internet of Things (IoT) devices. An energy harvesting system (EHS) powered by a PSC module with a backup [...] Read more.
The rapid rise in the power conversion efficiency (PCE) of perovskite solar cells (PSCs) has opened the door for diverse potential applications in powering indoor Internet of Things (IoT) devices. An energy harvesting system (EHS) powered by a PSC module with a backup Li-ion battery, which stores excess power at moments of high irradiances and delivers the stored power to drive the load during operation scenarios with low irradiances, has been designed. A DC-DC boost converter is engaged to match the voltage of the PSC and Li-ion battery, and maximum power point tracking (MPPT) is achieved by a perturb and observe (P&O) algorithm, which perturbs the photovoltaic (PV) system by adjusting its operating voltage and observing the difference in the output power of the PSC. Furthermore, the charging and discharging rate of the battery storage is controlled by a DC-DC buck–boost bidirectional converter with the incorporation of a proportional–integral (PI) controller. The bidirectional DC-DC converter operates in a dual mode, achieved through the anti-parallel connection of a conventional buck and boost converter. The proposed EHS utilizes DC-DC converters, MPPT algorithms, and PI control schemes. Three different case scenarios are modeled to investigate the system’s behavior under varying irradiances of 200 W/m2, 100 W/m2, and 50 W/m2. For all three cases with different irradiances, MPPT achieves tracking efficiencies of more than 95%. The laboratory-fabricated PSC operated at MPP can produce an output power ranging from 21.37 mW (50 W/m2) to 90.15 mW (200 W/m2). The range of the converter’s output power is between 5.117 mW and 63.78 mW. This power range can sufficiently meet the demands of modern low-energy IoT devices. Moreover, fully charged and fully discharged battery scenarios were simulated to study the performance of the system. Finally, the IoT load profile was simulated to confirm the potential of the proposed energy harvesting system in self-sustainable IoT applications. Upon review of the current literature, there are limited studies demonstrating a combination of EHS with PSCs as an indoor power source for IoT applications, along with a bidirectional DC-DC buck–boost converter to manage battery charging and discharging. The evaluation of the system performance presented in this work provides important guidance for the development and optimization of new-generation PV technologies like PSCs for practical indoor applications. Full article
(This article belongs to the Special Issue Recent Advances in Solar Cells and Photovoltaics)
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<p>PSC energy harvesting system block diagram.</p>
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<p>Conventional DC-DC boost converter circuit diagram.</p>
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<p>P&amp;O MPPT flow chart.</p>
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<p>Bidirectional DC-DC buck–boost converter.</p>
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<p>Diagram of battery control mechanism.</p>
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<p>The power consumption scale of common IoT devices. Reprinted with permission from [<a href="#B34-energies-18-01118" class="html-bibr">34</a>]. Copyright 2021 John Wiley and Sons.</p>
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<p>(<b>a</b>) A lab-fabricated PSC module being characterized under standard 1 sun illumination. (<b>b</b>) Four PSC modules are connected in a single frame for integrated operation.</p>
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<p>Modeling of PSC’s (<b>a</b>) I-V characteristic and (<b>b</b>) P-V characteristic under varying irradiance conditions.</p>
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<p>The graphs of the DC-DC boost converter at 200 W/m<sup>2</sup> irradiance: (<b>a</b>) input and (<b>b</b>) output power; (<b>c</b>) input and (<b>d</b>) output voltage.</p>
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<p>The graphs of the DC-DC boost converter at 100 W/m<sup>2</sup> irradiance: (<b>a</b>) input and (<b>b</b>) output power; (<b>c</b>) input and (<b>d</b>) output voltage.</p>
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<p>The graphs of the DC-DC boost converter at 50 W/m<sup>2</sup> irradiance: (<b>a</b>) input and (<b>b</b>) output power; (<b>c</b>) input and (<b>d</b>) output voltage.</p>
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<p>SOC and input power graphs for (<b>a</b>,<b>b</b>) a fully charged battery and (<b>c</b>,<b>d</b>) a fully discharged battery.</p>
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<p>The simulation result with consideration of the IoT load profile used in the proposed EHS.</p>
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26 pages, 3379 KiB  
Review
Solid-State Lithium Batteries: Advances, Challenges, and Future Perspectives
by Subin Antony Jose, Amethyst Gallant, Pedro Lechuga Gomez, Zacary Jaggers, Evan Johansson, Zachary LaPierre and Pradeep L. Menezes
Batteries 2025, 11(3), 90; https://doi.org/10.3390/batteries11030090 - 22 Feb 2025
Viewed by 454
Abstract
Solid-state lithium-ion batteries are gaining attention as a promising alternative to traditional lithium-ion batteries. By utilizing a solid electrolyte instead of a liquid, these batteries offer the potential for enhanced safety, higher energy density, and longer life cycles. The solid electrolyte typically consists [...] Read more.
Solid-state lithium-ion batteries are gaining attention as a promising alternative to traditional lithium-ion batteries. By utilizing a solid electrolyte instead of a liquid, these batteries offer the potential for enhanced safety, higher energy density, and longer life cycles. The solid electrolyte typically consists of a polymer matrix integrated with ceramic fillers, which can significantly boost ionic conductivity. Research efforts are currently focused on advancing materials for the battery’s three primary components: the electrolyte, anode, and cathode. Furthermore, innovative strategies are being developed to optimize the interfaces between these components, addressing key challenges in performance and durability. Cutting-edge manufacturing techniques are also being explored to improve production efficiency and reduce costs. With continued advancements, solid-state lithium-ion batteries are poised to become integral to next-generation technologies, including electric vehicles and wearable electronics. Full article
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<p>Key stability challenges in SSBs. Reproduced from [<a href="#B14-batteries-11-00090" class="html-bibr">14</a>], open access, MDPI, 2024.</p>
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<p>Enhancement strategies for all-solid-state lithium batteries. Reproduced with permission from [<a href="#B15-batteries-11-00090" class="html-bibr">15</a>].</p>
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<p>SSB vs. LIB: structural comparison.</p>
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<p>Different outcomes to different safety scenarios within the battery. Adapted from [<a href="#B83-batteries-11-00090" class="html-bibr">83</a>].</p>
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<p>Electrode buffer and sacrificial layers. Reproduced with permission from [<a href="#B98-batteries-11-00090" class="html-bibr">98</a>].</p>
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