三元运算
材料科学
电场
接受者
开路电压
电压
光电子学
化学物理
激子
静电学
工作(物理)
分子间力
有机太阳能电池
结晶
电势能
能量转换效率
电荷(物理)
密度泛函理论
能量(信号处理)
领域(数学)
三元数制
纳米技术
整改
太阳能电池
光伏系统
电流密度
太阳能
电位
能量收集
科技与社会
作者
Yongjie Cui,Anxu Cheng,Wenzhao Xiong,Zhibo Wang,Shenbo Zhu,Zaifei Ma,Huawei Hu
摘要
ABSTRACT In ternary all‐polymer organic solar cells (all‐PSCs), while the short‐circuit current density ( J SC ) and fill factor (FF) are enhanced, further device efficiency improvement is constrained by the large energy loss. Here, a wide‐bandgap guest donor PTO2 with deeper energy level is introduced into the PM6:PYIT system to resolve this issue. Theoretical calculations indicate that PTO2 exhibits a more negative electrostatic potential (ESP), enabling the formation of a strong intermolecular electric field when paired with the acceptor that displays a positive surface ESP, thereby facilitating efficient exciton dissociation. Experimentally, PTO2 endows complementary light absorption, optimizes the vertical composition distribution, balances the crystallization kinetics, and promotes tighter π – π stacking. Meanwhile, PTO2 can effectively enhance the built‐in electric field and reduce charge generation/recombination associated energy loss. Consequently, the ternary device achieves an optimal efficiency of 19.12% with an enhanced open circuit voltage ( V OC ) of 0.963 V without sacrificing J SC and FF compared to PM6:PYIT. This work highlights the crucial role of ESP modulation and provides a novel matching approach for high‐performance ternary all‐PSCs.
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