材料科学
光电子学
钙钛矿(结构)
光伏系统
载流子
超晶格
收缩(语法)
X射线光电子能谱
凝聚态物理
化学物理
化学
结晶学
物理
医学
生物
核磁共振
内科学
生态学
作者
Wenbin Li,Siraj Sidhik,Boubacar Traoré,Reza Asadpour,Jin Hou,Hao Zhang,Austin Fehr,Joseph Essman,Yafei Wang,Justin M. Hoffman,Ioannis Spanopoulos,Jared Crochet,Esther H. R. Tsai,Joseph Strzalka,Claudine Katan,Muhammad A. Alam,Mercouri G. Kanatzidis,Jacky Even,Jean‐Christophe Blancon,Aditya D. Mohite
标识
DOI:10.1038/s41565-021-01010-2
摘要
Understanding and tailoring the physical behaviour of halide perovskites under practical environments is critical for designing efficient and durable optoelectronic devices. Here, we report that continuous light illumination leads to >1% contraction in the out-of-plane direction in two-dimensional hybrid perovskites, which is reversible and strongly dependent on the specific superlattice packing. X-ray photoelectron spectroscopy measurements show that constant light illumination results in the accumulation of positive charges in the terminal iodine atoms, thereby enhancing the bonding character of inter-slab I-I interactions across the organic barrier and activating out-of-plane contraction. Correlated charge transport, structural and photovoltaic measurements confirm that the onset of the light-induced contraction is synchronized to a threefold increase in carrier mobility and conductivity, which is consistent with an increase in the electronic band dispersion predicted by first-principles calculations. Flux-dependent space-charge-limited current measurement reveals that light-induced interlayer contraction activates interlayer charge transport. The enhanced charge transport boosts the photovoltaic efficiency of two-dimensional perovskite solar cells up to 18.3% by increasing the device's fill factor and open-circuit voltage.
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