Al-Eid et al., 2014 - Google Patents
Facile synthesis of metal-free organic dyes featuring a thienylethynyl spacer for dye sensitized solar cellsAl-Eid et al., 2014
View HTML- Document ID
- 7079301094029625900
- Author
- Al-Eid M
- Lim S
- Park K
- Fitzpatrick B
- Han C
- Kwak K
- Hong J
- Cooke G
- Publication year
- Publication venue
- Dyes and Pigments
External Links
Snippet
In this article, we report the facile synthesis of metal-free dyes 6 and 7, their solution-based optical and redox properties and their use as sensitizers in dye-sensitized solar cells (DSSCs). Our studies indicate that the addition of the second thiophene unit in dye 7 …
- 239000000975 dye 0 title abstract description 85
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
- 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
-
- 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
- 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
- H01L51/005—Macromolecular systems with low molecular weight, e.g. cyanine dyes, coumarine dyes, tetrathiafulvalene
- H01L51/0062—Macromolecular systems with low molecular weight, e.g. cyanine dyes, coumarine dyes, tetrathiafulvalene aromatic compounds comprising a hetero atom, e.g.: N,P,S
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/06—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom containing only hydrogen and carbon atoms in addition to the ring nitrogen atom
-
- 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
- H01L51/42—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 specially adapted for sensing infra-red radiation, light, electro-magnetic radiation of shorter wavelength or corpuscular radiation and adapted for the conversion of the energy of such radiation into electrical energy or for the control of electrical energy by such radiation using organic materials as the active part, or using a combination of organic materials with other material as the active part; Multistep processes for their manufacture
Similar Documents
Publication | Publication Date | Title |
---|---|---|
Al-Eid et al. | Facile synthesis of metal-free organic dyes featuring a thienylethynyl spacer for dye sensitized solar cells | |
Yang et al. | Efficient solar cells based on porphyrin dyes with flexible chains attached to the auxiliary benzothiadiazole acceptor: suppression of dye aggregation and the effect of distortion | |
Baheti et al. | Fluorene-based sensitizers with a phenothiazine donor: effect of mode of donor tethering on the performance of dye-sensitized solar cells | |
Yang et al. | Influence of the donor size in D− π–A organic dyes for dye-sensitized solar cells | |
Saito et al. | Photo-sensitizing ruthenium complexes for solid state dye solar cells in combination with conducting polymers as hole conductors | |
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 | |
Chu et al. | Structural planarity and conjugation effects of novel symmetrical acceptor–donor–acceptor organic sensitizers on dye-sensitized solar cells | |
Gao et al. | Conjugation of selenophene with bipyridine for a high molar extinction coefficient sensitizer in dye-sensitized solar cells | |
Karthikeyan et al. | Highly efficient solid-state dye-sensitized TiO2 solar cells via control of retardation of recombination using novel donor-antenna dyes | |
Lee et al. | Novel D-π-A organic dyes with thieno [3, 2-b] thiophene-3, 4-ethylenedioxythiophene unit as a π-bridge for highly efficient dye-sensitized solar cells with long-term stability | |
Biswas et al. | Design of efficient metal-free organic dyes having an azacyclazine scaffold as the donor fragment for dye-sensitized solar cells | |
Gupta et al. | The effect of direct amine substituted push–pull oligothiophene chromophores on dye-sensitized and bulk heterojunction solar cells performance | |
Irgashev et al. | A facile and convenient synthesis and photovoltaic characterization of novel thieno [2, 3-b] indole dyes for dye-sensitized solar cells | |
Cheng et al. | Organic dyes containing indolodithienopyrrole unit for dye-sensitized solar cells | |
Misra et al. | Positional isomers of pyridine linked triphenylamine-based donor-acceptor organic dyes for efficient dye-sensitized solar cells | |
Tigreros et al. | Influence of acetylene-linked π-spacers on triphenylamine–fluorene dye sensitized solar cells performance | |
Qian et al. | Triazatruxene-based organic dyes containing a rhodanine-3-acetic acid acceptor for dye-sensitized solar cells | |
Mba et al. | Sensitization of nanocrystalline TiO2 with multibranched organic dyes and co (III)/(II) Mediators: Strategies to improve charge collection efficiency | |
Park et al. | An investigation of the role the donor moiety plays in modulating the efficiency of ‘donor-π-acceptor-π-acceptor’organic DSSCs | |
Qian et al. | Indeno [1, 2-b] indole-based organic dyes with different acceptor groups for dye-sensitized solar cells | |
Cho et al. | Novel organic sensitizers containing a bulky spirobifluorene unit for solar cell | |
Singh et al. | Fluorene-based organic dyes containing acetylene linkage for dye-sensitized solar cells | |
Iqbal et al. | Impact of hydroxy and octyloxy substituents of phenothiazine based dyes on the photovoltaic performance | |
Kim et al. | Electrochemical characterization of newly synthesized polyterthiophene benzoate and its applications to an electrochromic device and a photovoltaic cell | |
Mandal et al. | Metal-free bipolar/octupolar organic dyes for DSSC application: A combined experimental and theoretical approach |