材料科学
结晶
激子
有机太阳能电池
化学物理
重组
离解(化学)
堆积
光伏系统
有机半导体
光电子学
化学工程
聚合物
化学
凝聚态物理
物理化学
电气工程
有机化学
物理
生物化学
工程类
复合材料
基因
作者
Huarui Zhang,Guangliu Ran,Xinyue Cui,Yuqiang Liu,Zhe Yin,Dawei Li,Xueqing Ma,Wenlong Liu,Hao Lu,Rui Liu,Lei Cai,Wenkai Zhang,Siru Guo,Hongxiang Li,Jifa Yu,Yi Lin,Yahui Liu,Guanghao Lu,Zaifei Ma,Pei Cheng,Zhishan Bo
标识
DOI:10.1002/aenm.202302063
摘要
Abstract Although the advances in organic solar cells (OSCs) have been considerable, their efficiency is still limited by recombination losses. Photogenerated electrons and holes are generally bound as localized excitons in organic semiconductors. The transition from excitons into free charges requires diffusion and dissociation processes, in which parasitic recombination losses exist. Reducing these losses is necessary for highly efficient OSCs. The crystallization behavior of the active layers can influence the efficiency of exciton diffusion and dissociation. In this work, different additives are delicately designed to control the crystallization behavior. It is found that the crystallization quality of active layers can be improved by controlling the aggregation of nonfullerene acceptors. The π–π stacking of blend films becomes compact, meanwhile, the crystallization in the vertical direction is more uniform. These are beneficial to the diffusion and dissociation of excitons. As a consequence, recombination losses are reduced and power convention efficiencies (PCEs) are improved significantly. Meanwhile, the general applicability of the additive is demonstrated in various organic photovoltaic systems, in which a PCE of 19.3% is achieved in D18:BTP‐eC9‐4F OSCs. This work provides a facile strategy to reduce the recombination losses of excitons for efficient devices.
科研通智能强力驱动
Strongly Powered by AbleSci AI