Literature DB >> 20571668

Carbazole-based polymers for organic photovoltaic devices.

Jiaoli Li1, Andrew C Grimsdale.   

Abstract

Polymers based upon 2,7-disubstituted carbazole have recently become of great interest as electron-donating materials in organic photovoltaic devices. In this tutorial review the synthesis of such polymers and their relative performances in such devices are surveyed. In particular structure-property relationships are investigated and the potential for the rational design of materials for high efficiency solar cells is discussed. In the case of the 2,7-carbazole homopolymer it has been found that electron acceptors other than fullerenes produce higher energy conversion efficiencies. To get around possible problems with the build-up of charge density at the 3- and 6-positions and to improve the solar light harvesting ability of the polymers by reducing the bandgap, ladder- and step-ladder type 2,7-carbazole polymers have been synthesised. The fully ladderised polymers gave very poor results in devices, but efficiencies of over 1% have been obtained from a step-ladder polymer with a diindenocarbazole monomer unit. Donor-acceptor copolymers containing 2,7-carbazole donors and various electron-accepting comonomer units have been prepared. An efficiency of 6% has been reported from a device using such a copolymer and by suitable choice of the acceptor comonomer, polymers can be designed with potential theoretical power conversion efficiencies of 10%. While such efficiencies remain to be obtained, the results to date certainly suggest that carbazole-based polymers and copolymers are among the most promising materials yet proposed for obtaining high efficiency organic solar cells.

Entities:  

Year:  2010        PMID: 20571668     DOI: 10.1039/b915995a

Source DB:  PubMed          Journal:  Chem Soc Rev        ISSN: 0306-0012            Impact factor:   54.564


  10 in total

1.  Synthesis of carbazole-based dendritic conjugated polymer: a dual channel optical probe for the detection of I- and Hg2.

Authors:  Yimin Wu; Ling Zhang; Fudong Ma; Tao Ding; Ablikim Obolda
Journal:  Des Monomers Polym       Date:  2022-06-20       Impact factor: 3.718

2.  Theoretical design of low bandgap donor-acceptor (D-A) monomers for polymer solar cells: DFT and TD-DFT study.

Authors:  Said A H Vuai; Numbury Surendra Babu
Journal:  Des Monomers Polym       Date:  2021-05-05       Impact factor: 2.650

3.  3,6-Carbazole vs 2,7-carbazole: A comparative study of hole-transporting polymeric materials for inorganic-organic hybrid perovskite solar cells.

Authors:  Wei Li; Munechika Otsuka; Takehito Kato; Yang Wang; Takehiko Mori; Tsuyoshi Michinobu
Journal:  Beilstein J Org Chem       Date:  2016-07-07       Impact factor: 2.883

4.  Thermodynamic synthesis of solution processable ladder polymers.

Authors:  Jongbok Lee; Bharath Bangalore Rajeeva; Tianyu Yuan; Zi-Hao Guo; Yen-Hao Lin; Mohammed Al-Hashimi; Yuebing Zheng; Lei Fang
Journal:  Chem Sci       Date:  2015-11-06       Impact factor: 9.825

5.  Unusual light-driven amplification through unexpected regioselective photogeneration of five-membered azaheterocyclic AIEgen.

Authors:  Qiyao Li; Junyi Gong; Ying Li; Ruoyao Zhang; Haoran Wang; Jianquan Zhang; He Yan; Jacky W Y Lam; Herman H Y Sung; Ian D Williams; Ryan T K Kwok; Min-Hui Li; Jianguo Wang; Ben Zhong Tang
Journal:  Chem Sci       Date:  2020-10-19       Impact factor: 9.825

6.  Reversible Charge Trapping in Bis-Carbazole-Diimide Redox Polymers with Complete Luminescence Quenching Enabling Nondestructive Read-Out by Resonance Raman Spectroscopy.

Authors:  Luuk Kortekaas; Federico Lancia; Jorn D Steen; Wesley R Browne
Journal:  J Phys Chem C Nanomater Interfaces       Date:  2017-06-12       Impact factor: 4.126

7.  Construction of highly functionalized carbazoles via condensation of an enolate to a nitro group.

Authors:  Tej Narayan Poudel; Yong Rok Lee
Journal:  Chem Sci       Date:  2015-09-16       Impact factor: 9.825

8.  Synthesis of Carbazoles and Related Heterocycles from Sulfilimines by Intramolecular C-H Aminations.

Authors:  Xianhai Tian; Lina Song; A Stephen K Hashmi
Journal:  Angew Chem Int Ed Engl       Date:  2020-04-02       Impact factor: 15.336

9.  Visible Light Induced Metal-Free Carbene N-Carbazolation.

Authors:  Claire Empel; Frederic W Patureau; Rene M Koenigs
Journal:  J Org Chem       Date:  2019-08-15       Impact factor: 4.354

10.  Chemically Stable Carbazole-Based Imine Covalent Organic Frameworks with Acidochromic Response for Humidity Control Applications.

Authors:  Leisan Gilmanova; Volodymyr Bon; Leonid Shupletsov; Darius Pohl; Marcus Rauche; Eike Brunner; Stefan Kaskel
Journal:  J Am Chem Soc       Date:  2021-11-02       Impact factor: 15.419

  10 in total

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