Author
Listed:
- Shulin Chen
(Peking University
Harbin Institute of Technology)
- Changwei Wu
(Shenzhen Institute of Advanced Technology, Chinese Academy of Sciences)
- Bo Han
(Peking University)
- Zhetong Liu
(Peking University)
- Zhou Mi
(Shijiazhuang Tiedao University)
- Weizhong Hao
(Shijiazhuang Tiedao University)
- Jinjin Zhao
(Shijiazhuang Tiedao University)
- Xiao Wang
(Shenzhen Institute of Advanced Technology, Chinese Academy of Sciences
Southern University of Science and Technology)
- Qing Zhang
(Peking University)
- Kaihui Liu
(Peking University
Collaborative Innovation Center of Quantum Matter)
- Junlei Qi
(Harbin Institute of Technology)
- Jian Cao
(Harbin Institute of Technology)
- Jicai Feng
(Harbin Institute of Technology)
- Dapeng Yu
(South University of Science and Technology)
- Jiangyu Li
(Shenzhen Institute of Advanced Technology, Chinese Academy of Sciences
Southern University of Science and Technology
Southern University of Science and Technology)
- Peng Gao
(Peking University
Collaborative Innovation Center of Quantum Matter
Peking University)
Abstract
Understanding the atomic structure and structural instability of organic-inorganic hybrid perovskites is the key to appreciate their remarkable photoelectric properties and understand failure mechanism. Here, using low-dose imaging technique by direct-detection electron-counting camera in a transmission electron microscope, we investigate the atomic structure and decomposition pathway of CH3NH3PbI3 (MAPbI3) at the atomic scale. We successfully image the atomic structure of perovskite in real space under ultra-low electron dose condition, and observe a two-step decomposition process, i.e., initial loss of MA+ followed by the collapse of perovskite structure into 6H-PbI2 with their critical threshold doses also determined. Interestingly, an intermediate phase (MA0.5PbI3) with locally ordered vacancies can robustly exist before perovskite collapses, enlightening strategies for prevention and recovery of perovskite structure during the degradation. Associated with the structure evolution, the bandgap gradually increases from ~1.6 eV to ~2.1 eV. In addition, it is found that C-N bonds can be readily destroyed under irradiation, releasing NH3 and HI and leaving hydrocarbons. These findings enhance our understanding of the photoelectric properties and failure mechanism of MAPbI3, providing potential strategies into material optimization.
Suggested Citation
Shulin Chen & Changwei Wu & Bo Han & Zhetong Liu & Zhou Mi & Weizhong Hao & Jinjin Zhao & Xiao Wang & Qing Zhang & Kaihui Liu & Junlei Qi & Jian Cao & Jicai Feng & Dapeng Yu & Jiangyu Li & Peng Gao, 2021.
"Atomic-scale imaging of CH3NH3PbI3 structure and its decomposition pathway,"
Nature Communications, Nature, vol. 12(1), pages 1-7, December.
Handle:
RePEc:nat:natcom:v:12:y:2021:i:1:d:10.1038_s41467-021-25832-9
DOI: 10.1038/s41467-021-25832-9
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Citations
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Cited by:
- Weilun Li & Mengmeng Hao & Ardeshir Baktash & Lianzhou Wang & Joanne Etheridge, 2023.
"The role of ion migration, octahedral tilt, and the A-site cation on the instability of Cs1-xFAxPbI3,"
Nature Communications, Nature, vol. 14(1), pages 1-11, December.
- Shuxian Du & Hao Huang & Zhineng Lan & Peng Cui & Liang Li & Min Wang & Shujie Qu & Luyao Yan & Changxu Sun & Yingying Yang & Xinxin Wang & Meicheng Li, 2024.
"Inhibiting perovskite decomposition by a creeper-inspired strategy enables efficient and stable perovskite solar cells,"
Nature Communications, Nature, vol. 15(1), pages 1-11, December.
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