甲脒
钙钛矿(结构)
卤化物
材料科学
碘化物
八面体
吸附
能量转换效率
化学物理
不稳定性
铋
相对湿度
相变
格子(音乐)
接受者
电极
无机化学
化学工程
化学
熵(时间箭头)
纳米技术
六方晶系
相(物质)
作者
Tianyin Miao,Sanwan Liu,Xia Lei,Yong Zhang,Wenhua Li,Qisen Zhou,Yi-Xiang Wang,Nikita A. Emelianov,Victoria V. Ozerova,Valeria S. Bolshakova,W WANG,Zheng Zhou,Z G Zhu,Lanlu Lu,Z J Chen,Jingyuan Ma,Erxiang Xu,L S Wang,Li Yunfei,Zhengtian Tan
出处
期刊:Science
[American Association for the Advancement of Science]
日期:2026-05-14
卷期号:392 (6799): 742-748
被引量:4
标识
DOI:10.1126/science.aeb9953
摘要
A critical limitation of formamidinium lead iodide (FAPbI 3 ) perovskite solar cells (PSCs) lies in the intrinsic instability of the ionic–covalent Pb–I octahedral lattice, relative to the unfavorable hexagonal δ-phase under operating conditions. We report an entropy-regulating molecular-lock strategy using 1-pyridin-3-ylmethyl-piperazine hydrochloride (3-PMPCl). Strong interactions between the perovskite lattice surface and 3-PMPCl modulate the rotational freedom of organic cations and suppress the detrimental entropy increase associated with [PbI 6 ] 4− octahedra disorder or expansion. This entropy-favored environment intrinsically increases the phase transition energy barrier. The uniform distribution and strong adsorption of 3-PMPCl stabilize the α-phase under elevated temperature and humidity conditions. We achieved a certified power conversion efficiency (PCE) of 27.6% in FAPbI 3 -based PSCs. However, the operational stability of such champion devices remains below the state of the art. Adopting a stable bismuth electrode addresses this issue with a slight reduction in efficiency, yielding a device that retains 93.0% of its initial PCE (26.8%) after 1011 hours at 85°C under 1-sun illumination.
科研通智能强力驱动
Strongly Powered by AbleSci AI