材料科学
制作
钙钛矿(结构)
结晶度
三碘化物
能量转换效率
成核
热稳定性
钙钛矿太阳能电池
化学工程
带隙
晶体生长
退火(玻璃)
纳米技术
矿物学
光电子学
结晶学
物理化学
电解质
化学
复合材料
色素敏化染料
电极
医学
替代医学
有机化学
病理
工程类
作者
Guanghui Yu,Ke‐Jian Jiang,Wei‐Min Gu,Xinning Jiao,Tangyue Xue,Yiqiang Zhang,Yanlin Song
标识
DOI:10.1021/acsami.2c23289
摘要
All-inorganic cesium lead triiodide (CsPbI3) perovskite has received increasing attention due to its intrinsic thermal stability and suitable band gap for photovoltaic applications. However, it is difficult to deposit high-quality pure-phase CsPbI3 films using CsI and PbI2 as precursors due to the rapid nucleation and crystal growth by the solution coating method. Here, a simple cation-exchange approach is employed to fabricate all-inorganic 3D CsPbI3 perovskite, where 1D ethylammonium lead (EAPbI3) perovskite is first solution-deposited and then transformed to 3D CsPbI3 via ion exchange between EA+ and Cs+ during thermal annealing. The large space between the PbI3– skeletons in 1D EAPbI3 favors the cation interdiffusion and exchange for the formation of pure-phase 3D CsPbI3 with full compactness and high crystallinity and orientation. The resulting CsPbI3 film exhibits a low trap density of state and high charge mobility, and the perovskite solar cell shows a power-conversion efficiency of 18.2% with enhanced stability. This strategy provides an alternative and promising fabrication route for the fabrication of high-quality all-inorganic perovskite devices.
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