Literature DB >> 23030837

Bithiopheneimide-dithienosilole/dithienogermole copolymers for efficient solar cells: information from structure-property-device performance correlations and comparison to thieno[3,4-c]pyrrole-4,6-dione analogues.

Xugang Guo1, Nanjia Zhou, Sylvia J Lou, Jonathan W Hennek, Rocío Ponce Ortiz, Melanie R Butler, Pierre-Luc T Boudreault, Joseph Strzalka, Pierre-Olivier Morin, Mario Leclerc, Juan T López Navarrete, Mark A Ratner, Lin X Chen, Robert P H Chang, Antonio Facchetti, Tobin J Marks.   

Abstract

Rational creation of polymeric semiconductors from novel building blocks is critical to polymer solar cell (PSC) development. We report a new series of bithiopheneimide-based donor-acceptor copolymers for bulk-heterojunction (BHJ) PSCs. The bithiopheneimide electron-deficiency compresses polymer bandgaps and lowers the HOMOs--essential to maximize power conversion efficiency (PCE). While the dithiophene bridge progression R(2)Si→R(2)Ge minimally impacts bandgaps, it substantially alters the HOMO energies. Furthermore, imide N-substituent variation has negligible impact on polymer opto-electrical properties, but greatly affects solubility and microstructure. Grazing incidence wide-angle X-ray scattering (GIWAXS) indicates that branched N-alkyl substituents increased polymer π-π spacings vs linear N-alkyl substituents, and the dithienosilole-based PBTISi series exhibits more ordered packing than the dithienogermole-based PBTIGe analogues. Further insights into structure-property-device performance correlations are provided by a thieno[3,4-c]pyrrole-4,6-dione (TPD)-dithienosilole copolymer PTPDSi. DFT computation and optical spectroscopy show that the TPD-based polymers achieve greater subunit-subunit coplanarity via intramolecular (thienyl)S···O(carbonyl) interactions, and GIWAXS indicates that PBTISi-C8 has lower lamellar ordering, but closer π-π spacing than does the TPD-based analogue. Inverted BHJ solar cells using bithiopheneimide-based polymer as donor and PC(71)BM as acceptor exhibit promising device performance with PCEs up to 6.41% and V(oc) > 0.80 V. In analogous cells, the TPD analogue exhibits 0.08 V higher V(oc) with an enhanced PCE of 6.83%, mainly attributable to the lower-lying HOMO induced by the higher imide group density. These results demonstrate the potential of BTI-based polymers for high-performance solar cells, and provide generalizable insights into structure-property relationships in TPD, BTI, and related polymer semiconductors.

Entities:  

Year:  2012        PMID: 23030837     DOI: 10.1021/ja3081583

Source DB:  PubMed          Journal:  J Am Chem Soc        ISSN: 0002-7863            Impact factor:   15.419


  6 in total

1.  Theoretical design of donor-acceptor conjugated copolymers based on furo-, thieno-, and selenopheno[3,4-c] thiophene-4,6-dione and benzodithiophene units for organic solar cells.

Authors:  Xiaorui Liu; Rongxing He; Wei Shen; Ming Li
Journal:  J Mol Model       Date:  2013-07-31       Impact factor: 1.810

2.  Theoretical investigations on enhancing the performance of terminally diketopyrrolopyrrole-based small-molecular donors in organic solar cell applications.

Authors:  Xiaorui Liu; Chengzhi Huang; Wei Shen; Rongxing He; Ming Li
Journal:  J Mol Model       Date:  2015-12-21       Impact factor: 1.810

3.  Morphology Evolution in High-Performance Polymer Solar Cells Processed from Nonhalogenated Solvent.

Authors:  Wanzhu Cai; Peng Liu; Yaocheng Jin; Qifan Xue; Feng Liu; Thomas P Russell; Fei Huang; Hin-Lap Yip; Yong Cao
Journal:  Adv Sci (Weinh)       Date:  2015-05-26       Impact factor: 16.806

4.  Direct (Hetero)Arylation for the Synthesis of Molecular Materials: Coupling Thieno[3,4-c]pyrrole-4,6-dione with Perylene Diimide to Yield Novel Non-Fullerene Acceptors for Organic Solar Cells.

Authors:  Thomas A Welsh; Audrey Laventure; Gregory C Welch
Journal:  Molecules       Date:  2018-04-17       Impact factor: 4.411

5.  π-Conjugated stannole copolymers synthesised by a tin-selective Stille cross-coupling reaction.

Authors:  Isabel-Maria Ramirez Y Medina; Markus Rohdenburg; Pascal Rusch; Daniel Duvinage; Nadja C Bigall; Anne Staubitz
Journal:  Mater Adv       Date:  2021-03-27

6.  Small Molecules Derived from Thieno[3,4-c]pyrrole-4,6-dione (TPD) and Their Use in Solution Processed Organic Solar Cells.

Authors:  Cesar Garcias-Morales; Daniel Romero-Borja; José-Luis Maldonado; Arián E Roa; Mario Rodríguez; J Pablo García-Merinos; Armando Ariza-Castolo
Journal:  Molecules       Date:  2017-09-30       Impact factor: 4.411

  6 in total

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