材料科学
接受者
有机太阳能电池
能量转换效率
激子
活动层
光化学
共轭体系
光伏系统
光电子学
聚合物太阳能电池
聚合物
纳米技术
化学物理
图层(电子)
化学
电气工程
物理
凝聚态物理
薄膜晶体管
工程类
复合材料
作者
Furong Shi,Pengzhi Guo,Xianfeng Qiao,Yao Guo,Tao Zhang,Qi Lu,Qian Wang,Xiaofeng Wang,Jasurbek Rikhsibaev,Ergang Wang,Chunfeng Zhang,Young‐Wan Kwon,Han Young Woo,Hongbin Wu,Jianhui Hou,Dongge Ma,Ardalan Armin,Yuguang Ma,Yangjun Xia
标识
DOI:10.1002/adma.202212084
摘要
Nonfullerene-acceptor-based organic solar cells (NFA-OSCs) are now set off to the 20% power conversion efficiency milestone. To achieve this, minimizing all loss channels, including nonradiative photovoltage losses, seems a necessity. Nonradiative recombination, to a great extent, is known to be an inherent material property due to vibrationally induced decay of charge-transfer (CT) states or their back electron transfer to the triplet excitons. Herein, it is shown that the use of a new conjugated nitroxide radical polymer with 2,2,6,6-tetramethyl piperidine-1-oxyl side groups (GDTA) as an additive results in an improvement of the photovoltaic performance of NFA-OSCs based on different active layer materials. Upon the addition of GDTA, the open-circuit voltage (VOC ), fill factor (FF), and short-circuit current density (JSC ) improve simultaneously. This approach is applied to several material systems including state-of-the-art donor/acceptor pairs showing improvement from 15.8% to 17.6% (in the case of PM6:Y6) and from 17.5% to 18.3% (for PM6:BTP-eC9). Then, the possible reasons behind the observed improvements are discussed. The results point toward the suppression of the CT state to triplet excitons loss channel. This work presents a facile, promising, and generic approach to further improve the performance of NFA-OSCs.
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