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• W4308005313 abstract "In this study, single-crystalline methylammonium lead tribromide (MAPbBr₃, CH₃NH₃PbBr₃) flakes with a higher theoretical specific capacity than methylammonium lead iodide (MAPbI₃, CH₃NH₃PbI₃), the prototype of organic/inorganic hybrid perovskite, were synthesized by the inverse temperature crystallization method. The combination of the additive-free electrophoretic deposition (EPD) system and the single crystal fabrication method provided a fundamental understanding of the electrochemical properties associated with the lithium-ion storage mechanism in which the formation of the lithiated-phase (Li_x:CH₃NH₃PbBr₃) and the conversion reaction causes significant irreversible capacity, reducing battery cycle stability. The conversion reaction in MAPbBr₃ was observed to be the main factor for high irreversible capacity, while the capacity due to the alloying reaction was more significant. The occurrence of the capacity due to the conversion reaction in the slurry system demonstrates that the additives worked as a buffer to relieve the stress associated with the formation of the lithiated phase, which was not observed in the MAPbBr₃ EPD film. As part of an investigation of the active material/electrolyte in terms of cycling stability, the problem of structural instability was addressed by replacing the lithium salt and organic solvent that are components of the electrolyte. Our findings shed light on the intrinsic electrochemical properties of MAPbBr₃ during lithiation/delithiation in the charging/discharging process, eliminating the complex effect caused by the MAPbBr₃/additive mixture. Structural stability at the MAPbBr₃/electrolyte interface was probed by varying the solvent and lithium salt." @default.
• W4308005313 created "2022-11-07" @default.
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• W4308005313 date "2022-11-05" @default.
• W4308005313 modified "2023-09-30" @default.
• W4308005313 title "Lithiation/De-lithiation through Conversion and Alloying Reactions in MAPbBr₃ Single Crystal Flake Li-ion Battery Anodes" @default.
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• W4308005313 doi "https://doi.org/10.3365/kjmm.2022.60.11.845" @default.
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