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Updated: Jun 13, 2026

Monovalent Cation Doping of CH3NH3PbI3 for Efficient Perovskite Solar Cells
Published on: March 19, 2017
Interstitial Iodine Induced Deep-Trap-Pinning Suppresses Self-Healing at the TiO2/Perovskite Interface
Kai-Ping Wang1, Hui Liang1, Xi-Meng Tang1
1Institute of Quantum Physics, Hunan Key Laboratory of Nanophotonics and Devices, Hunan Key Laboratory of Super-Microstructure and Ultrafast Process, School of Physics, Central South University, Changsha 410083, China.
None:
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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