材料科学
有机太阳能电池
共轭体系
共聚物
溶解度
兴奋剂
电导率
轨道能级差
电子迁移率
化学工程
光伏系统
光电子学
聚合物
分子
有机化学
物理化学
复合材料
生态学
化学
工程类
生物
作者
Lisi Yang,Shuaishuai Shen,Xiang Chen,Huan Wei,Dongdong Xia,Chaowei Zhao,Ningfang Zhang,Yuanyuan Hu,Weiwei Li,Hao Xin,Jinsheng Song
标识
DOI:10.1002/adfm.202303603
摘要
Abstract The electron transport layer (ETL) is a critical component in achieving high device performance and stability in organic solar cells. Conjugated polyelectrolytes (CPEs) have become an attractive alternative due to film‐forming properties and ease of preparation. However, p‐type CPEs generally exhibit poor charge mobility and conductivity, incorporation of electron‐withdrawing units forming alternated D‐A conjugated backbone can make up for these deficiencies. Herein, the ratio of electron withdrawing moieties are further increased and two poly(A1‐alt‐A2) typed PIIDNDI‐Br and PDPPNDI‐Br based on the combination of naphthalene diimide (NDI) with isoindigo (IID) or diketopyrrolopyrrole (DPP) via direct arylation polycondensation are synthesized. These CPEs possess excellent alcohol solubility, a suitable lowest unocuppied molecular orbital energy level, and work function tunability. Surprisingly, the incorporation of IID and DPP units generate distinct self‐doping behaviors, which are confirmed by UV–vis absorption and ESR spectra. However, no matter doped or undoped, both CPEs present better charge‐transporting properties and conductivity when utilized as ETLs. The PIIDNDI‐Br and PDPPNDI‐Br display good universal compatibility with the blend of PM6:Y6 and PM6:L8‐BO, and PCEs of 18.32% and 18.36% are obtained, respectively, which also present excellent storage stability. In short, the combination of two different acceptors demonstrates an efficient strategy to design highly efficient ETLs for high performance photovoltaic devices.
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