Literature DB >> 19753339

Triarylamine: a promising core unit for efficient photovoltaic materials.

Zhijun Ning1, He Tian.   

Abstract

Triarylamine has been widely used in opto- and electro-active materials for its good electron donating and transporting capability, as well as its special propeller starburst molecular structure. Recently, organic photovoltaic functional materials with triarylamine as electron donor have aroused great interest and become the focus of intensive research in the field of solar cells. These materials have significantly reinforced the conversion efficiency of next-generation solar cells, especially dye sensitized solar cells. This Feature Article describes new synthetic methods and the application of starburst triarylamines, highlighting the applications in photovoltaic and optoelectrical fields.

Entities:  

Year:  2009        PMID: 19753339     DOI: 10.1039/b908802d

Source DB:  PubMed          Journal:  Chem Commun (Camb)        ISSN: 1359-7345            Impact factor:   6.222


  29 in total

1.  Synthesis and optical properties of various thienyl derivatives of pyrene.

Authors:  Krzysztof R Idzik; Tobias Licha; Vladimír Lukeš; Peter Rapta; Jaroslaw Frydel; Mario Schaffer; Eric Taeuscher; Rainer Beckert; Lothar Dunsch
Journal:  J Fluoresc       Date:  2013-08-06       Impact factor: 2.217

2.  The effect of anchoring group number on molecular structures and absorption spectra of triphenylamine sensitizers: a computational study.

Authors:  Jie Xu; Ligen Zhu; Lei Wang; Li Liu; Zikui Bai; Luoxin Wang; Weilin Xu
Journal:  J Mol Model       Date:  2011-08-12       Impact factor: 1.810

3.  Palladium-Catalyzed Coupling of Functionalized Primary and Secondary Amines with Aryl and Heteroaryl Halides: Two Ligands Suffice in Most Cases.

Authors:  Debabrata Maiti; Brett P Fors; Jaclyn L Henderson; Yoshinori Nakamura; Stephen L Buchwald
Journal:  Chem Sci       Date:  2011-01-01       Impact factor: 9.825

4.  Comparative study on electronic structures and optical properties of indoline and triphenylamine dye sensitizers for solar cells.

Authors:  Cai-Rong Zhang; Li Liu; Jian-Wu Zhe; Neng-Zhi Jin; Li-Hua Yuan; Yu-Hong Chen; Zhi-Qiang Wei; You-Zhi Wu; Zi-Jiang Liu; Hong-Shan Chen
Journal:  J Mol Model       Date:  2012-12-28       Impact factor: 1.810

5.  Synthesis of Strongly Fluorescent Imidazole Derivatives: Structure Property Studies, Halochromism and Fluorescent Photoswitching.

Authors:  Anu Kundu; Subramanian Karthikeyan; Dohyun Moon; Savarimuthu Philip Anthony
Journal:  J Fluoresc       Date:  2019-11-14       Impact factor: 2.217

6.  Improvement of photovoltaic performance by substituent effect of donor and acceptor structure of TPA-based dye-sensitized solar cells.

Authors:  Natalia Inostroza; Fernando Mendizabal; Ramiro Arratia-Pérez; Carlos Orellana; Cristian Linares-Flores
Journal:  J Mol Model       Date:  2016-01-07       Impact factor: 1.810

7.  Fused Methoxynaphthyl Phenanthrimidazole Semiconductors as Functional Layer in High Efficient OLEDs.

Authors:  Jayaraman Jayabharathi; Periyasamy Ramanathan; Chockalingam Karunakaran; Venugopal Thanikachalam
Journal:  J Fluoresc       Date:  2015-11-19       Impact factor: 2.217

8.  Theoretical study on p-type D-π-A sensitizers with modified π-spacers for dye-sensitized solar cells.

Authors:  Wen Yan; Kadali Chaitanya; Zhi-Dan Sun; Xue-Hai Ju
Journal:  J Mol Model       Date:  2018-02-24       Impact factor: 1.810

9.  Rational synthesis of interpenetrated 3D covalent organic frameworks for asymmetric photocatalysis.

Authors:  Xing Kang; Xiaowei Wu; Xing Han; Chen Yuan; Yan Liu; Yong Cui
Journal:  Chem Sci       Date:  2019-12-19       Impact factor: 9.825

10.  Synthesis, spectroscopy, and computational analysis of photoluminescent bis(aminophenyl)-substituted thiophene derivatives.

Authors:  Daniel Lumpi; Ernst Horkel; Felix Plasser; Hans Lischka; Johannes Fröhlich
Journal:  Chemphyschem       Date:  2013-02-26       Impact factor: 3.102

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