材料科学
能量转换效率
聚合物
光伏系统
化学工程
溶剂
分散性
有机太阳能电池
电子迁移率
聚合物太阳能电池
等效串联电阻
接受者
化学物理
纳米技术
光电子学
高分子化学
复合材料
有机化学
电压
生物
物理
工程类
化学
量子力学
凝聚态物理
生态学
作者
Yan Wang,Han Yu,Xin Wu,Dan Zhao,Shoufeng Zhang,Xinhui Zou,Bo Li,Danpeng Gao,Zhen Li,Xinxin Xia,Xiankai Chen,Xinhui Lu,He Yan,Chu‐Chen Chueh,Alex K.‐Y. Jen,Zonglong Zhu
标识
DOI:10.1002/aenm.202202729
摘要
Abstract All‐polymer solar cells (all‐PSCs) have achieved impressive progress in photovoltaic performance and stabilities recently. However, their power conversion efficiencies (PCEs) still trail that of small‐molecular acceptor‐based organic solar cells (>19%) mainly because of the inferior fill factor (FF). Herein, a combined homo hydrocarbon solvent and sequential deposition (SD) strategy is presented to boost the FF of rigid all‐PSCs to 77.7% and achieve a superior PCE of 17.7% with excellent stability, which is among the highest efficiencies reported for all‐PSCs thus far. Meanwhile, a remarkable PCE of 14.5% is realized for flexible all‐PSCs with outstanding mechanical stability. The blend film morphologies measurements suggest that the SD method enables the formation of an ideal pseudo‐bilayer film with bicontinuous interdigitated structure and ordered polymer packing. The numerical simulation result indicates that the FF enhancement mainly results from the efficient exciton diffusion dynamics, increased carrier mobilities, and more balanced electron/hole mobility ratio induced by the developed SD method. This is also confirmed by the FF loss analysis, which manifests that the reduced series resistance and increased shunt resistance are the main reasons for the reduction of FF loss. This work provides a promising strategy to fabricate highly efficient and stable all‐PSCs to promote their future development and practical manufacturing.
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