材料科学
混溶性
有机太阳能电池
能量转换效率
接受者
聚合物
形状记忆合金*
延展性(地球科学)
拉伤
化学工程
富勒烯
分子
光伏系统
电子受体
复合材料
纳米技术
光电子学
光化学
有机化学
化学
工程类
医学
生态学
蠕动
物理
数学
组合数学
内科学
生物
凝聚态物理
作者
Zhenye Wang,Di Zhang,Lvpeng Yang,Omar Allam,Yerun Gao,Yang Su,Meichen Xu,Songmin Mo,Qinghe Wu,Zhi Wang,Junfeng Liu,Jiayi He,Rui Li,Xingwang Jia,Zhilin Li,Long Yang,Mark Weber,Yu Yu,Xinliang Zhang,Tobin J. Marks
出处
期刊:Science
[American Association for the Advancement of Science]
日期:2025-01-23
卷期号:387 (6732): 381-387
被引量:2
标识
DOI:10.1126/science.adp9709
摘要
Emerging wearable devices would benefit from integrating ductile photovoltaic light-harvesting power sources. In this work, we report a small-molecule acceptor (SMA), also known as a non–fullerene acceptor (NFA), designed for stretchable organic solar cell ( s -OSC) blends with large mechanical compliance and performance. Blends of the organosilane-functionalized SMA BTP-Si4 with the polymer donor PNTB6-Cl achieved a power conversion efficiency (PCE) of >16% and ultimate strain (ε u ) of >95%. Typical SMAs suppress OSC blend ductility, but the addition of BTP-Si4 enhances it. Although BTP-Si4 is less crystalline than other SMAs, it retains considerable electron mobility and is highly miscible with PNTB6-Cl and is essential for enhancing ε u . Thus, s -OSCs with PCE > 14% and operating normally under various deformations (>80% PCE retention under an 80% strain) were demonstrated. Analysis of several SMA-polymer blends revealed general molecular structure–miscibility–stretchability relationships for designing ductile blends.
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