材料科学
光伏系统
极限抗拉强度
有机太阳能电池
弹性体
复合材料
聚合物
工作(物理)
能量转换效率
纳米技术
光电子学
机械工程
电气工程
工程类
作者
Saimeng Li,Mengyuan Gao,Kangkang Zhou,Xin Li,Kaihu Xian,Wenchao Zhao,Yu Chen,Chunyong He,Long Ye
标识
DOI:10.1002/adma.202307278
摘要
Abstract Organic solar cells (OSCs) have potential for applications in wearable electronics. Except for high power conversion efficiency (PCE), excellent tensile properties and mechanical stability are required for achieving high‐performance wearable OSCs, while the present metrics barely meet the stretchable requirements. Herein, this work proposes a facile and low‐cost strategy for constructing intrinsically stretchable OSCs by introducing a readily accessible polymer elastomer as a diluent for all‐polymer photovoltaic blends. Remarkably, record‐high stretchability with a fracture strain of up to 1000% and mechanical stability with elastic recovery >90% under cyclic tensile tests are realized in the OSCs active layers for the first time. Specifically, the tensile properties of best‐performing all‐polymer photovoltaic blends are increased by up to 250 times after blending. Previously unattainable performance metrics (fracture strain >50% and PCE >10%) are achieved simultaneously for the resulting photovoltaic films. Furthermore, an overall evaluation parameter y is proposed for the efficiency‐cost‐ stretchability balance of photovoltaic blend films. The y value of dilute‐absorber system is two orders of magnitude greater than those of prior state‐of‐the‐art systems. Additionally, intrinsically stretchable devices are prepared to showcase the mechanical stability. Overall, this work offers a new avenue for constructing and comprehensively evaluating intrinsically stretchable organic electronic films.
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