[go: up one dir, main page]

Gasiorowski et al., 2015 - Google Patents

Porphyrin containing lipophilic amide groups as a photosensitizer for dye-sensitized solar cells

Gasiorowski et al., 2015

View HTML
Document ID
8380985510349246409
Author
Gasiorowski J
Pootrakulchote N
Reanprayoon C
Jaisabuy K
Vanalabhpatana P
Sariciftci N
Thamyongkit P
Publication year
Publication venue
RSC Advances

External Links

Snippet

In this study, synthesis and investigation of a novel zinc-porphyrin derivative bearing C24- containing amide groups for potential use in dye-sensitized solar cells (DSSCs) are presented. According to absorption spectra and electrochemical data, the target porphyrin …
Continue reading at pubs.rsc.org (HTML) (other versions)

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
    • 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
    • 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
    • H01L51/0085—Transition metal complexes, e.g. Ru(II)polypyridine complexes comprising Iridium
    • 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
    • H01L51/0077—Coordination compounds, e.g. porphyrin
    • H01L51/0089—Metal complexes comprising Lanthanides or Actinides, e.g. Eu
    • 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
    • H01L51/005—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
    • H01L51/0071—Polycyclic condensed heteroaromatic hydrocarbons
    • H01L51/0072—Polycyclic condensed heteroaromatic hydrocarbons comprising only nitrogen in the heteroaromatic polycondensed ringsystem, e.g. phenanthroline, carbazole
    • 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
    • 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
    • H01L51/50—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 light emission, e.g. organic light emitting diodes [OLED] or polymer light emitting devices [PLED];

Similar Documents

Publication Publication Date Title
Sandroni et al. First application of the HETPHEN concept to new heteroleptic bis (diimine) copper (I) complexes as sensitizers in dye sensitized solar cells
Sirohi et al. Novel di-anchoring dye for DSSC by bridging of two mono anchoring dye molecules: a conformational approach to reduce aggregation
Shinpuku et al. Synthesis and characterization of novel cyclometalated iridium (III) complexes for nanocrystalline TiO2-based dye-sensitized solar cells
El-Shafei et al. A novel carbazole-based dye outperformed the benchmark dye N719 for high efficiency dye-sensitized solar cells (DSSCs)
Ning et al. Novel iridium complex with carboxyl pyridyl ligand for dye-sensitized solar cells: High fluorescence intensity, high electron injection efficiency?
Stengel et al. “Click-chemistry” approach in the design of 1, 2, 3-triazolyl-pyridine ligands and their Ru (ii)-complexes for dye-sensitized solar cells
Dragonetti et al. Simple novel cyclometallated iridium complexes for potential application in dye-sensitized solar cells
Pasunooti et al. Synthesis, characterization and application of trans-D–B–A-porphyrin based dyes in dye-sensitized solar cells
Tan et al. Novel zinc porphyrin sensitizers for dye-sensitized solar cells: Synthesis and spectral, electrochemical, and photovoltaic properties
Panda et al. A new family of A 2 B 2 type porphyrin derivatives: synthesis, physicochemical characterization and their application in dye-sensitized solar cells
Mao et al. Design of Bodipy based organic dyes for high-efficient dye-sensitized solar cells employing double electron acceptors
Dragonetti et al. A new thiocyanate-free cyclometallated ruthenium complex for dye-sensitized solar cells: Beneficial effects of substitution on the cyclometallated ligand
Bonomo et al. KuQuinones as sensitizers for NiO based p-type dye-sensitized solar cells
Hara et al. New Ru (II) phenanthroline complex photosensitizers having different number of carboxyl groups for dye-sensitized solar cells
Higashino et al. π-Expanded dibenzo-BODIPY with near-infrared light absorption: Investigation of photosensitizing properties of NiO-based p-type dye-sensitized solar cells
Stengel et al. Click‐Functionalized Ru (II) Complexes for Dye‐Sensitized Solar Cells
Giribabu et al. A new familiy of heteroleptic ruthenium (ii) polypyridyl complexes for sensitization of nanocrystalline TiO 2 films
Hussain et al. A comparative study of Ru (II) cyclometallated complexes versus thiocyanated heteroleptic complexes: thermodynamic force for efficient dye regeneration in dye-sensitized solar cells and how low could it be?
Athanas et al. Co-sensitization of ruthenium (II) dye-sensitized solar cells by coumarin based dyes
Lyu et al. Molecular engineering of ruthenium-diacetylide organometallic complexes towards efficient green dye for DSSC
Luechai et al. Photosensitizing triarylamine-and triazine-cored porphyrin dimers for dye-sensitized solar cells
Wu et al. Thiocyanate-free asymmetric ruthenium (II) dye sensitizers containing azole chromophores with near-IR light-harvesting capacity
Anthonysamy et al. Molecular design and synthesis of ruthenium (II) sensitizers for highly efficient dye-sensitized solar cells
Cheema et al. Monodentate pyrazole as a replacement of labile NCS for Ru (II) photosensitizers: Minimum electron injection free energy for dye-sensitized solar cells
Shahroosvand et al. Red electroluminescence of ruthenium sensitizer functionalized by sulfonate anchoring groups