X射线光电子能谱
氢氧化物
碱性电池
氧化还原
电化学
化学
无机化学
碱土金属
X射线吸收光谱法
材料科学
吸收光谱法
电解质
化学工程
电极
金属
冶金
物理
物理化学
量子力学
工程类
作者
Sathya Narayanan Jagadeesan,Gabriel D. Barbosa,Fenghua Guo,Lihua Zhang,Milinda Abeykoon,Gihan Kwon,Daniel Olds,C. Heath Turner,Xiaowei Teng
标识
DOI:10.1021/acs.chemmater.3c01496
摘要
Rechargeable alkaline iron batteries that constitute environmentally benign electrolytes and earth-abundant industrial materials are desirable green solutions for large-scale energy storage. As one of the most abundant metal elements in the earth's crust, iron (Fe) can satisfy nearly all criteria for low-cost and safe battery electrodes. However, challenges in achieving reversible Fe redox impede their extensive implementation in modern energy supply systems. This study revealed that Cl-anion insertion into Fe(OH)2 layered double hydroxide (LDH) formed a green rust intermediate phase with the formula [Fe22+Fe13+(HO–)6]+[Cl]−, which assisted a high Fe(OH)2/FeOOH conversion reaction (64.7%) and improved cycling stability. This new iron redox chemistry was validated by operando X-ray diffraction, electrochemical testing, X-ray absorption spectroscopy (XAS), X-ray photoelectron spectroscopy (XPS) analysis, scanning transmission electron microscopy–energy-dispersive X-ray spectroscopy (STEM-EDS) mapping, and molecular dynamics (MD) simulations. Our study provides new insight into designing LDH materials for high-capacity alkaline iron batteries.
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