普鲁士蓝
材料科学
氧化还原
X射线光电子能谱
水溶液
电化学
傅里叶变换红外光谱
电解质
单斜晶系
无机化学
化学工程
电极
化学
结晶学
晶体结构
物理化学
工程类
冶金
作者
Marcos Lucero,Davis B. Armitage,Xin Yang,Sean K. Sandstrom,Mason Lyons,Ryan C. Davis,George E. Sterbinsky,Namhyung Kim,David Reed,Xiulei Ji,Xiaolin Li,Zhenxing Feng
标识
DOI:10.1021/acsami.3c07304
摘要
Aqueous Na-ion batteries using Prussian blue materials have inherent advantages in safety, material sustainability, and economic cost. However, it is challenging to obtain long-term cycling stability because many redox reactions have poor intrinsic stability in water. Here, we demonstrate reversible Fe2.4+ to Fe3+ redox reaction of Prussian blue electrodes cycled in a 17 m NaClO4 water-in-salt electrolyte. The cubic phase c-Na1.17Fe[Fe(CN)6]·0.35H2O) derived from monoclinic Prussian blue (m-Na1.88Fe[Fe(CN)6]·0.7H2O) through ball milling delivers excellent cycling stability of >18,000 cycles with >90% capacity retention at the 10C rate. The specific capacity is ∼75 and ∼67 mAh/g at 1C and 10C rates, respectively. Systematic characterizations including electron microscopy, X-ray diffraction, Fourier-transform infrared spectroscopy, X-ray photoelectron spectroscopy, and X-ray absorption spectroscopy have verified the phase transition and iron oxidation state evolution, revealing the mechanism that enables the material's high rate and long durability as the battery cathode.
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