材料科学
活动层
有机太阳能电池
偶极子
流体学
能量转换效率
接受者
退火(玻璃)
热的
光伏系统
光电子学
烷基
纳米技术
化学物理
太阳能电池
形态学(生物学)
化学工程
噻唑
聚合物太阳能电池
力矩(物理)
图层(电子)
钝化
能量转换
熔点
低临界溶液温度
偏移量(计算机科学)
俘获
作者
Tao Zhang,Chentong Liao,Yutao Lu,Xingjian Dai,H Wang,Jiahao Zhang,Weilin Zhou,Min Deng,Xiaopeng Xu,Qiang Peng
摘要
ABSTRACT Precise morphological control during both film formation and post‐thermal annealing (TA) remains a formidable challenge for layer‐by‐layer (LbL) processed organic solar cells (OSCs). Conventional solid additives often suffer from functional stagnation during the critical TA step due to their rigid thermal properties. Herein, we develop an innovative “annealing‐activated liquid mediator” strategy for multi‐level morphological control. Such a type of solid additive of BTTz has been designed and engineered by flanking a 5,6‐difluorobenzo[d]thiazole core with thiazole rings at the 4,7 positions. This constructs multiple non‐covalent interactions to optimize the primary aggregation of the D18 donor during deposition. Crucially, a 2‐hexyloctyl alkyl chain precisely tunes the BTTz melting point to 72°C. During TA treatment (80°C–120°C), the melted BTTz acts as a transient fluidic medium, driving the ordered secondary self‐assembly of L8‐BO acceptor into a D18 network. Consequently, the BTTz‐treated devices achieve an outstanding power conversion efficiency (PCE) of 20.03%, representing a ∼10% enhancement over the control one. This dynamic phase‐transition paradigm provides a robust pathway for precise morphology manipulation in high‐performance OSCs.
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