Ravivarma et al., 2018 - Google Patents
Interfacial charge transport studies and fabrication of high performance DSSC with ethylene cored unsymmetrical dendrimers as quasi electrolytesRavivarma et al., 2018
- Document ID
- 4964897977152046348
- Author
- Ravivarma M
- Kumar K
- Rajakumar P
- Pandurangan A
- Publication year
- Publication venue
- Journal of Molecular Liquids
External Links
Snippet
In this paper, authors focus the synthesis of conjugated unsymmetrical stilbenoid dendrimers by Heck and Horner-Wadsworth-Emmons coupling. In UV–visible absorption spectrum, the intensity of the absorption increases with increase in the generation of dendrimers. Further …
- 239000000412 dendrimer 0 title abstract description 121
Classifications
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02E—REDUCTION OF GREENHOUSE GASES [GHG] EMISSION, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
- Y02E10/00—Energy generation through renewable energy sources
- Y02E10/50—Photovoltaic [PV] energy
- Y02E10/54—Material technologies
- Y02E10/549—Material technologies organic PV cells
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02E—REDUCTION OF GREENHOUSE GASES [GHG] EMISSION, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
- Y02E10/00—Energy generation through renewable energy sources
- Y02E10/50—Photovoltaic [PV] energy
- Y02E10/54—Material technologies
- Y02E10/542—Dye sensitized solar cells
-
- H—ELECTRICITY
- H01—BASIC ELECTRIC ELEMENTS
- H01G—CAPACITORS; CAPACITORS, RECTIFIERS, DETECTORS, SWITCHING DEVICES OR LIGHT-SENSITIVE DEVICES, OF THE ELECTROLYTIC TYPE
- H01G9/00—Electrolytic capacitors, rectifiers, detectors, switching devices, light-sensitive or temperature-sensitive devices; Processes of their manufacture
- H01G9/20—Light-sensitive devices
- H01G9/2027—Light-sensitive devices comprising an oxide semiconductor electrode
- H01G9/2031—Light-sensitive devices comprising an oxide semiconductor electrode comprising titanium oxide, e.g. TiO2
-
- H—ELECTRICITY
- H01—BASIC ELECTRIC ELEMENTS
- H01G—CAPACITORS; CAPACITORS, RECTIFIERS, DETECTORS, SWITCHING DEVICES OR LIGHT-SENSITIVE DEVICES, OF THE ELECTROLYTIC TYPE
- H01G9/00—Electrolytic capacitors, rectifiers, detectors, switching devices, light-sensitive or temperature-sensitive devices; Processes of their manufacture
- H01G9/20—Light-sensitive devices
- H01G9/2059—Light-sensitive devices comprising an organic dye as the active light absorbing material, e.g. adsorbed on an electrode or dissolved in solution
-
- H—ELECTRICITY
- H01—BASIC ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES; ELECTRIC SOLID STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H01L51/00—Solid state devices using organic materials as the active part, or using a combination of organic materials with other materials as the active part; Processes or apparatus specially adapted for the manufacture or treatment of such devices, or of parts thereof
- H01L51/0032—Selection of organic semiconducting materials, e.g. organic light sensitive or organic light emitting materials
- H01L51/0077—Coordination compounds, e.g. porphyrin
- H01L51/0084—Transition metal complexes, e.g. Ru(II)polypyridine complexes
- H01L51/0086—Transition metal complexes, e.g. Ru(II)polypyridine complexes comprising Ruthenium
Similar Documents
Publication | Publication Date | Title |
---|---|---|
Farre et al. | Second generation of diketopyrrolopyrrole dyes for NiO-based dye-sensitized solar cells | |
Grisorio et al. | Anchoring stability and photovoltaic properties of new D (-π-A) 2 dyes for dye-sensitized solar cell applications | |
Paramasivam et al. | Tuning the photovoltaic performance of benzocarbazole-based sensitizers for dye-sensitized solar cells: a joint experimental and theoretical study of the influence of π-spacers | |
Baheti et al. | Simple triarylamine-based dyes containing fluorene and biphenyl linkers for efficient dye-sensitized solar cells | |
Bodedla et al. | Benzimidazole-branched isomeric dyes: effect of molecular constitution on photophysical, electrochemical, and photovoltaic properties | |
Pastore et al. | Computational modeling of stark effects in organic dye-sensitized TiO2 heterointerfaces | |
Lu et al. | A near-infrared dithieno [2, 3-a: 3′, 2′-c] phenazine-based organic co-sensitizer for highly efficient and stable quasi-solid-state dye-sensitized solar cells | |
Zhang et al. | Comparative study on pyrido [3, 4-b] pyrazine-based sensitizers by tuning bulky donors for dye-sensitized solar cells | |
She et al. | Novel ruthenium sensitizers with a phenothiazine conjugated bipyridyl ligand for high-efficiency dye-sensitized solar cells | |
Ravivarma et al. | Interfacial charge transport studies and fabrication of high performance DSSC with ethylene cored unsymmetrical dendrimers as quasi electrolytes | |
Ramkumar et al. | Synthesis of bianchored metal free organic dyes for dye sensitized solar cells | |
Cheng et al. | Organic dyes containing indolodithienopyrrole unit for dye-sensitized solar cells | |
Shi et al. | New ruthenium sensitizers featuring bulky ancillary ligands combined with a dual functioned coadsorbent for high efficiency dye-sensitized solar cells | |
Al-Eid et al. | Facile synthesis of metal-free organic dyes featuring a thienylethynyl spacer for dye sensitized solar cells | |
Singh et al. | Fluorene-based organic dyes containing acetylene linkage for dye-sensitized solar cells | |
Selvaraj et al. | Effect of 1-substituted 2-(pyridin-2-yl)-1 H-Benzo [d] imidazole ligand-coordinated copper and cobalt complex redox electrolytes on performance of Ru (II) dye-based dye-sensitized solar cells | |
Sil et al. | Orthogonally functionalized donor/acceptor homo-and heterodimeric dyes for dye-sensitized solar cells: an approach to introduce panchromaticity and control the charge recombination | |
Chou et al. | Structurally simple and easily accessible perylenes for dye-sensitized solar cells applicable to both 1 sun and dim-light environments | |
Wu et al. | Metal-free organic dyes with di (1-benzothieno)[3, 2-b: 2′, 3′-d] pyrrole as a donor for efficient dye-sensitized solar cells: Effect of mono-and bi-anchors on photovoltaic performance | |
Kim et al. | Electrochemical characterization of newly synthesized polyterthiophene benzoate and its applications to an electrochromic device and a photovoltaic cell | |
Maglione et al. | Tuning optical absorption in pyran derivatives for DSSC | |
Baldoli et al. | Benzodithiophene based organic dyes for DSSC: Effect of alkyl chain substitution on dye efficiency | |
Damaceanu et al. | Heteroatom-mediated performance of dye-sensitized solar cells based on T-shaped molecules | |
Li et al. | New benzothiadiazole-based dyes incorporating dithieno [3, 2-b: 2′, 3′-d] pyrrole (DTP) π-linker for dye-sensitized solar cells with different electrolytes | |
Ma et al. | Impact of π-conjugation configurations on the photovoltaic performance of the quinoxaline-based organic dyes |