结晶度
有机太阳能电池
材料科学
化学工程
能量转换效率
相(物质)
光致发光
光谱学
纳米技术
光伏系统
工作(物理)
固溶体
烷基
聚合物
原子力显微镜
形态学(生物学)
聚合物太阳能电池
合理设计
太阳能电池
漫反射红外傅里叶变换
机制(生物学)
作者
Huaipu Cui,Yanfeng Liu,Yu He,Xiuyan Wang,Tianmeng Zhang,Kai Wu,Lin Hu,Yingzhi Jin,Shumei Sun,Han Zuilhof,Zaifang Li,Hao Lü
标识
DOI:10.1021/acs.jpclett.5c03273
摘要
Incorporating solid additives is an effective strategy to regulate the morphologies of active layers and optimize the performance of organic solar cells (OSCs), yet their molecular-level mechanisms remain elusive. Here, three halogenated solid additives, namely, 1,8-dichloronaphthalene, 1,8-dibromonaphthalene, and 1,8-diiodonaphthalene, are investigated for their effect on PM6:Y6 blends. All three enhance the power conversion efficiency (PCE) of the devices, with 1,8-dibromonaphthalene yielding the highest value. Ex situ atomic force microscopy and in situ photoluminescence measurements reveal that the improved performance originates from favorable phase separation driven by promoted Y6 aggregation. Grazing incidence wide-angle X-ray scattering and interface-specific sum frequency generation spectroscopy further show that this favorable morphology stems from the enhanced crystallinity and increased ordering of alkyl side chains in both PM6 and Y6. Our work advances the fundamental understanding of the working mechanism of OSCs mediated by solid additives and offers guidance for the rational design of new solid additives for OSCs.
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