Photovoltaic donor-acceptor conjugated polymers with minimally substituted acceptor moieties

被引:11
作者
Schmatz, Brian [1 ]
Pelse, Ian [1 ]
Advincula, Abigail [1 ]
Zhang, Junxiang [1 ]
Marder, Seth R. [1 ]
Reynolds, John R. [1 ]
机构
[1] Georgia Inst Technol, Georgia Tech Polymer Network, Ctr Organ Photon & Elect, Sch Chem & Biochem,Sch Mat Sci & Engn, Atlanta, GA 30332 USA
关键词
Organic photovoltaics; Organic solar cells; Donor-acceptor polymers; Thieno[3,4-c]pyrrole-4,6-dione; SOLAR-CELLS; SIDE-CHAINS; SEMICONDUCTING POLYMERS; MORPHOLOGY CONTROL; PERFORMANCE; AGGREGATION; COPOLYMERS; FULLERENES; IMIDE;
D O I
10.1016/j.orgel.2019.02.020
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
A novel family of conjugated donor-acceptor (D-A) copolymers designed with comparatively small methyl substituted acceptor units was synthesized for use as donor phase materials in bulk heterojunction (BHJ) organic photovoltaic (OPV) applications. These polymers make use of common acceptor moieties thieno [3,4-c] pyrrole-4,6-dione (TPD), diketopyrrolopyrrole (DPP), and isoindigo (iI) with methyl side chains to provide sterically unhindered sites for enhanced interactions with a molecular acceptor (MA), either PC71BM or ITIC in this study. The resulting polymers P(T4-TPD-M), P(T4-DPP-M), and P(T4-iI-M) were utilized in BHJ OPV devices where the highest performing D-A polymer, P(T4-TPD-M), obtained a maximum PCE of 7.5% with PC71BM and 4.0% with ITIC. These results indicate that minimally-sized methyl side chain derivatives of TPD, DPP, and iI can be useful acceptor moieties in D-A polymer systems, and the impact of sterics on the acceptor moiety can be elucidated in future studies through modification of the methyl side chain to bulkier aliphatic substituents.
引用
收藏
页码:280 / 284
页数:5
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