材料科学
光电流
热稳定性
接受者
有机太阳能电池
二聚体
单体
活动层
聚合物太阳能电池
图层(电子)
光化学
聚合物
能量转换效率
光电子学
化学工程
纳米技术
有机化学
化学
复合材料
薄膜晶体管
物理
工程类
凝聚态物理
作者
Chia‐Hua Tsai,Fang-Ning Li,Chuang-Yi Liao,Yu‐Yang Su,Kuen‐Wei Tsai,Yu‐Tang Hsiao,Yi‐Ming Chang
标识
DOI:10.1021/acsami.3c03073
摘要
Incorporation of a non-fullerene acceptor (NFA) into an organic bulk-heterojunction currently has realized the extendable spectral response and high photocurrent generation in organic photodiodes. However, to allow these organic materials to be industrially commercialized, the thermal stability which enables the materials to survive under the process integration and operation needs to be considered. Generally, NFA small molecules showed high crystallinity, which aggregated through heating and led to the poor thermal stability. To tackle the thermal stability issue of highly efficient NFAs, two IDIC-based NFA dimers─IDIC-T Dimer and IDIC-TT Dimer─were designed, synthesized, and characterized; the thermal stability of the BHJ layer incorporating these dimer molecules was evaluated and compared with that of the BHJ layer using the monomer, IDIC-4Cl, as acceptors. Eventually, a power conversion efficiency of 9.44% was achieved for organic photovoltaic devices based on the NFA dimer. The dimers also showed remarkable thermal stability than the IDIC-4Cl monomer, which provided a promising direction for the polymer/small-molecule system in organic photodiodes for industrial practicability.
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