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Electrochemical Performance of Orthorhombic CsPbI(3) Perovskite in Li-Ion Batteries
A facile solution process was employed to prepare CsPbI(3) as an anode material for Li-ion batteries. Rietveld refinement of the X-ray data confirms the orthorhombic phase of CsPbI(3) at room temperature. As obtained from bond valence calculations, strained bonds between Pb and I are identified with...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8510073/ https://www.ncbi.nlm.nih.gov/pubmed/34640106 http://dx.doi.org/10.3390/ma14195718 |
Sumario: | A facile solution process was employed to prepare CsPbI(3) as an anode material for Li-ion batteries. Rietveld refinement of the X-ray data confirms the orthorhombic phase of CsPbI(3) at room temperature. As obtained from bond valence calculations, strained bonds between Pb and I are identified within PbI(6) octahedral units. Morphological study shows that the as-prepared δ-CsPbI(3) forms a nanorod-like structure. The XPS analysis confirm the presence of Cs (3d, 4d), Pb (4d, 4f, 5d) and I (3p, 3d, 4d). The lithiation process involves both intercalation and conversion reactions, as confirmed by cyclic voltammetry (CV) and first-principles calculations. Impedance spectroscopy coupled with the distribution function of relaxation times identifies charge transfer processes due to Li metal foil and anode/electrolyte interfaces. An initial discharge capacity of 151 mAhg(−1) is found to continuously increase to reach a maximum of ~275 mAhg(−1) at 65 cycles, while it drops to ~240 mAhg(−1) at 75 cycles and then slowly decreases to 235 mAhg(−1) at 100 cycles. Considering the performance and structural integrity during electrochemical performance, δ-CsPbI(3) is a promising material for future Li-ion battery (LIB) application. |
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