材料科学
碘化物
钙钛矿(结构)
卤化物
扩散
钋
钝化
三卤化物
化学工程
氧化物
纳米技术
无机化学
高分子化学
热力学
化学
冶金
工程类
物理
图层(电子)
作者
Haipeng Zeng,Lin Li,Fengxiang Liu,Min Li,Shujing Zhang,Xin Zheng,Long Luo,Shuai You,Yang Zhao,Rui Guo,Zhongmiao Gong,Rong Huang,Zhe Li,Ti Wang,Yi Cui,Yaoguang Rong,Xiong Li
标识
DOI:10.1002/aenm.202102820
摘要
Abstract Long‐term stability has become the major obstacle for the successful large‐scale application of perovskites devices. Owing to the ionic nature of metal‐halide perovskites, the interfacial ion diffusion can induce irreversible degradation under operational conditions, which presents a great challenge to realize stable perovskite solar modules. Here, a diphenylphosphine oxide compound, ethane‐1,2‐diylbis(diphenylphosphine oxide) (DPPO) is introduced to coordinate with lead iodide and form a cross‐linked 1D Pb 3 I 6 ‐DPPO (1D‐PbI 2 ) complex. These judiciously designed cross‐linked nonionic low‐dimensional lead halide/organic adducts can passivate the defects of perovskite while acting as a robust ion diffusion barrier, thus significantly improving the electronic quality and intrinsic stability of perovskite films. As a result, high‐performance inverted (p‐i‐n) solar modules with a champion efficiency approaching 19% (a certified stabilized efficiency of 17.8%) for active device areas above 17 cm 2 without the use of antisolvents, accompanied by outstanding operational stability under heat stress and continuous illumination are achieved.
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