期刊
NPG ASIA MATERIALS
卷 14, 期 1, 页码 -出版社
NATURE PORTFOLIO
DOI: 10.1038/s41427-022-00395-3
关键词
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资金
- National Natural Science Foundation of China [22072045, 21603073, 21574043]
- Xing-Fu-Zhi-Hua Foundation of ECNU
- Microscale Magnetic Resonance Platform of ECNU
This study compares the effects of bromine anion and dimethylamine cation alloying on the structure and properties of FAPbI3 perovskite. It demonstrates that DMA-incorporated FAPbI3 perovskites exhibit improved structural stability and photovoltaic performance while maintaining the original bandgap energy. The incorporation of DMA cations constrains the dynamic space of neighboring FA cations, increasing their interaction with the inorganic lattice and stabilizing the lattice structure. This work provides an efficient method for improving the phase stability of FAPbI3 perovskite materials and offers a plausible molecular mechanism for the stability induced by DMA-FA alloying.
Applications of organic-inorganic formamidinium (FA) lead triiodide (FAPbl(3)) perovskites in high-efficiency solar cells often suffer from spontaneous alpha-to-delta phase transitions. However, current efforts to inhibit this phenomenon based on simple cation and anion alloying strategies continue to suffer from unintended consequences, such as unfavorable shifts in the bandgap energy and unwanted phase separation during operation. The present work compares the effects of bromine (Br) anion and dimethylamine (DMA) cation alloying on the structure and properties of FAPbl(3) perovskite in detail. DMA-incorporated FAPbl(3) perovskites show significantly improved structural stability and photovoltaic performance, while the inherent bandgap energy of the original material is maintained. Rigorous analyses demonstrate that the relatively large size and free isotropic motion of the incorporated DMA cations constrain the dynamic space of neighboring FA cations, which increases the degree to which the FA cations interact with the inorganic lattice and therefore stabilizes the Pbl(6) lattice structure without significant lattice distortion. Hence, this work demonstrates an efficient method for improving the phase stability of FAPbl(3) perovskite materials while providing a plausible molecular mechanism for the stability engendered by the alloying of DMA and FA.
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