材料科学
表面改性
钙钛矿(结构)
钝化
成核
晶界
退火(玻璃)
晶粒生长
粒度
离子键合
化学工程
相(物质)
纳米技术
矿物学
复合材料
离子
热力学
有机化学
微观结构
图层(电子)
化学
工程类
物理
作者
Zhaobing Zeng,Jing Zhang,Xinlei Gan,Hongrui Sun,Minghui Shang,Dagang Hou,Chaojie Lu,Renjie Chen,Yuejin Zhu,Liyuan Han
标识
DOI:10.1002/aenm.201801050
摘要
Abstract The phase instability and large energy loss are two obstacles to achieve stable and efficient inorganic‐CsPbI 3− x Br x perovskite solar cells. In this work, stable cubic perovskite (α)‐phase CsPbI 2 Br is successfully achieved by Pb(Ac) 2 functioning at the grain boundary under low temperature. Ac − strongly coordinates with CsPbI 2 Br to stabilize the α‐phase and also make the grain size smaller and film uniform by fast nucleation. PbO is formed in situ at the grain boundary by decomposing Pb(Ac) 2 at high‐temperature annealing. The semiconducting PbO effectively passivates the surface states, reduces the interface recombination, and promotes the charge transport in CsPbI 2 Br perovskite solar cells. A 12% efficiency and good stability are obtained for in situ PbO‐passivated CsPbI 2 Br solar cells, while Pb(Ac) 2 ‐passivated device exhibits 8.7% performance and the highest stability, much better than the control device with 8.5% performance and inferior stability. This article highlights the extrinsic ionic grain boundary functionalization to achieve stable and efficient inorganic CsPbI 3− x Br x materials and the devices.
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