极化子
钙钛矿(结构)
材料科学
偶极子
化学物理
凝聚态物理
存水弯(水管)
电子
化学
结晶学
物理
量子力学
气象学
有机化学
作者
Kai-Ping Wang,Hui Liang,Xi-Meng Tang,Bo Wen,Chuan‐Jia Tong,Oleg V. Prezhdo
标识
DOI:10.1021/acs.jpclett.5c02430
摘要
Defects significantly influence charge transport in CH3NH3PbI3 (MAPbI3) perovskite solar cells, particularly at interfaces. Using quantum dynamics simulation, we reveal a distinct interstitial iodine (Ii) defect behavior at different positions in the TiO2/MAPbI3 system. In the perovskite bulk-like region, Ii exhibits high mobility and dissociates detrimental iodine trimers, facilitating small-to-large polaron transition and promoting shallow trap formation. In contrast, the interfacial Ii defect enhances local structural rigidity due to its strong interaction with undercoordinated Ti atoms and MA molecular dipoles, which unexpectedly pins the deep trap state and suppresses its inherent self-healing capability. This leads to polaron localization and accelerates nonradiative recombination by 2 orders of magnitude. The results reveal the mechanism of deep-trap-pinning due to an interstitial Ii defect at perovskite interfaces, which offers theoretical guidance for minimizing charge losses in highly efficient perovskite solar cells.
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