三碘化物
钙钛矿(结构)
能量转换效率
材料科学
铯
兴奋剂
光电子学
格子(音乐)
化学物理
化学
无机化学
电极
结晶学
物理化学
电解质
色素敏化染料
物理
声学
作者
Hsinhan Tsai,Reza Asadpour,Jean‐Christophe Blancon,Constantinos C. Stoumpos,Olivier Durand,Joseph Strzalka,Bo Chen,Rafael Verduzco,Pulickel M. Ajayan,Sergei Tretiak,Jacky Even,Muhammad Ashraf Alam,Mercouri G. Kanatzidis,Wanyi Nie,Aditya D. Mohite
出处
期刊:Science
[American Association for the Advancement of Science (AAAS)]
日期:2018-04-05
卷期号:360 (6384): 67-70
被引量:624
标识
DOI:10.1126/science.aap8671
摘要
Light-induced structural dynamics plays a vital role in the physical properties, device performance, and stability of hybrid perovskite–based optoelectronic devices. We report that continuous light illumination leads to a uniform lattice expansion in hybrid perovskite thin films, which is critical for obtaining high-efficiency photovoltaic devices. Correlated, in situ structural and device characterizations reveal that light-induced lattice expansion benefits the performances of a mixed-cation pure-halide planar device, boosting the power conversion efficiency from 18.5 to 20.5%. The lattice expansion leads to the relaxation of local lattice strain, which lowers the energetic barriers at the perovskite-contact interfaces, thus improving the open circuit voltage and fill factor. The light-induced lattice expansion did not compromise the stability of these high-efficiency photovoltaic devices under continuous operation at full-spectrum 1-sun (100 milliwatts per square centimeter) illumination for more than 1500 hours.
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