Development of a D–π–A dye with benzothienopyridine as the electron-withdrawing anchoring group for dye-sensitized solar cells
出版年份 2014 全文链接
标题
Development of a D–π–A dye with benzothienopyridine as the electron-withdrawing anchoring group for dye-sensitized solar cells
作者
关键词
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出版物
Journal of Materials Chemistry A
Volume 2, Issue 10, Pages 3293-3296
出版商
Royal Society of Chemistry (RSC)
发表日期
2014-01-06
DOI
10.1039/c3ta15067d
参考文献
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- (2013) Yousuke Ooyama et al. CHEMICAL COMMUNICATIONS
- Photovoltaic performance of dye-sensitized solar cells based on D–π–A type BODIPY dye with two pyridyl groups
- (2013) Yousuke Ooyama et al. NEW JOURNAL OF CHEMISTRY
- Dye-sensitized solar cells based on a functionally separated D–π–A fluorescent dye with an aldehyde as an electron-accepting group
- (2013) Yousuke Ooyama et al. NEW JOURNAL OF CHEMISTRY
- Stable Dyes Containing Double Acceptors without COOH as Anchors for Highly Efficient Dye-Sensitized Solar Cells
- (2012) Jiangyi Mao et al. ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
- 8-Hydroxylquinoline as a strong alternative anchoring group for porphyrin-sensitized solar cells
- (2012) Hongshan He et al. CHEMICAL COMMUNICATIONS
- Nitro group as a new anchoring group for organic dyes in dye-sensitized solar cells
- (2012) Jiayan Cong et al. CHEMICAL COMMUNICATIONS
- Porphyrin-sensitized solar cells
- (2012) Lu-Lin Li et al. CHEMICAL SOCIETY REVIEWS
- Photophysical and Electrochemical Properties, and Molecular Structures of Organic Dyes for Dye-Sensitized Solar Cells
- (2012) Yousuke Ooyama et al. CHEMPHYSCHEM
- D-D-π-A organic dyes containing 4,4′-di(2-thienyl)triphenylamine moiety for efficient dye-sensitized solar cells
- (2012) Ming-Dao Zhang et al. PHYSICAL CHEMISTRY CHEMICAL PHYSICS
- A new organic dye bearing aldehyde electron-withdrawing group for dye-sensitized solar cell
- (2012) Jin Tang et al. SOLAR ENERGY
- Photophysical, electrochemical and photovoltaic properties of dye sensitized solar cells using a series of pyridyl functionalized porphyrin dyes
- (2012) Dimitra Daphnomili et al. RSC Advances
- Dye-Sensitized Solar Cells Based On Donor-Acceptor π-Conjugated Fluorescent Dyes with a Pyridine Ring as an Electron-Withdrawing Anchoring Group
- (2011) Yousuke Ooyama et al. ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
- Dye-Sensitized Solar Cells Based on Donor-π-Acceptor Fluorescent Dyes with a Pyridine Ring as an Electron-Withdrawing-Injecting Anchoring Group
- (2011) Yousuke Ooyama et al. CHEMISTRY-A EUROPEAN JOURNAL
- Porphyrin-Sensitized Solar Cells with Cobalt (II/III)-Based Redox Electrolyte Exceed 12 Percent Efficiency
- (2011) A. Yella et al. SCIENCE
- Highly Efficient Mesoscopic Dye-Sensitized Solar Cells Based on Donor-Acceptor-Substituted Porphyrins
- (2010) Takeru Bessho et al. ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
- Dye-Sensitized Solar Cells
- (2010) Anders Hagfeldt et al. CHEMICAL REVIEWS
- Improvement of dye-sensitized solar cells: what we know and what we need to know
- (2010) Zhijun Ning et al. Energy & Environmental Science
- Synthesis of Functionalized Dibenzothiophenes - An Efficient Three-Step Approach Based on Pd-Catalyzed C-C and C-S Bond Formations
- (2010) Tue Heesgaard Jepsen et al. EUROPEAN JOURNAL OF ORGANIC CHEMISTRY
- Metal-Free Organic Dyes for Dye-Sensitized Solar Cells: From Structure: Property Relationships to Design Rules
- (2009) Amaresh Mishra et al. ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
- Triarylamine: a promising core unit for efficient photovoltaic materials
- (2009) Zhijun Ning et al. CHEMICAL COMMUNICATIONS
- Molecular Designs and Syntheses of Organic Dyes for Dye-Sensitized Solar Cells
- (2009) Yousuke Ooyama et al. EUROPEAN JOURNAL OF ORGANIC CHEMISTRY
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