材料科学
掺杂剂
钙钛矿(结构)
电子迁移率
带隙
聚合物
共轭体系
接受者
光电子学
兴奋剂
纳米技术
化学工程
凝聚态物理
复合材料
物理
工程类
作者
Zilong Zhang,Lusheng Liang,Longhui Deng,Lu Ren,Nan Zhao,Jianhua Huang,Yaming Yu,Peng Gao
标识
DOI:10.1021/acsami.0c21729
摘要
As a critical component in perovskite solar cells (PSCs), hole-transporting materials (HTMs) have been extensively explored. To develop efficient dopant-free HTMs for PSCs, a decent hole mobility (>10 –3 cm 2 V –1 s –1 ) is critically essential, which is, however, seldom reported. In this work, we introduce two novel donor–acceptor (D–A) type conjugated polymers ( PDTPC-1 and PDTPC-2 ) with narrow bandgap unit, i.e., fused dithienopicenocarbazole ( DTPC ), as the donor building block and benzo[ c ][1,2,5]thiadiazole derivatives as the acceptors. The highly planar and strong electron-donating DTPC endows the polymers with superior hole mobility up to ∼4 × 10 –3 cm 2 V –1 s –1 . Because of the better energy alignment with perovskite and excellent film-forming property, PSCs with PDTPC-1 as HTM show an appreciably enhanced PCE of ∼17% in dopant-free PSCs along with improved device stability as opposed to PDTPC-2 . Our work revealed for the first time that the introduction of narrow bandgap DTPC in D–A polymers could achieve remarkably high hole mobility in the pristine form, favoring the application in dopant-free PSCs.
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