材料科学
钙钛矿(结构)
串联
共轭体系
带隙
光电子学
化学工程
复合材料
聚合物
工程类
作者
Jianwei Chen,Zhuojia Lin,Hongyu Min,Kezhou Fan,Honggang Chen,Shibing Zou,Yitong Xu,Xiaoshuai Wu,Penggang Yin,Haining Chen,Lin Guo,Xinhui Lu,Man Yu Lam,Sergeev A. Aleksandr,Kam Sing Wong,Keyou Yan
标识
DOI:10.1002/aenm.202500309
摘要
Abstract Compared to single‐junction perovskite solar cells (PSCs), all‐perovskite tandem solar cells (PTSCs) offer higher power conversion efficiencies (PCEs). However, the substantial open‐circuit voltage ( V OC ) loss of wide‐bandgap (WBG) perovskite sub‐cells limits the efficiency due to the interface defect and halide segregation. In this study, 6‐hydroxy‐2‐naphthalenecarboxylic acid (HNA) is employed to construct cross‐linked network by the H‐bond and conjugated interaction to engineer the interface and suppress halide segregation. Enhanced Photoluminescence (PL) intensity and reduced quai‐Fermi level splitting (QFLS) loss indicate that the unique molecular conformation of HNA facilitates the process of the dense crosslinked film, which greatly enhances the passivation effect. Meanwhile, the strong π‐π interactions accelerate the charge transport at the WBG perovskite/C 60 interface, effectively suppressing the non‐radiative recombination. The 1.78 eV WBG PSCs achieve a V OC of 1.35 V and a PCE of 19.92% and deliver T 80 = 1100 h by maximum power point track (MPPT). In combination with narrow‐bandgap (NBG) sub‐cells, PTSCs exhibit a V OC of 2.13 V, a PCE of 28.25%, and T 80 of 500 h. This work provides a self‐assembled interlayer strategy to develop highly efficient and stable WBG sub‐cells for PTSCs.
科研通智能强力驱动
Strongly Powered by AbleSci AI