假电容
材料科学
氮化钒
钒
阳极
氧化还原
钠
X射线光电子能谱
钠离子电池
储能
氮化物
无机化学
化学工程
纳米技术
法拉第效率
电极
电化学
超级电容器
冶金
化学
功率(物理)
物理
物理化学
图层(电子)
量子力学
工程类
作者
Ruijia Liu,Lingxu Yang,Wenjun Wang,Enyue Zhao,Bao-Tian Wang,Xue Zhang,Huijun Liu,Chaoliu Zeng
标识
DOI:10.1016/j.mtener.2023.101300
摘要
Structure-stable anodes are essential for achieving long-cycling stability in sodium-ion batteries. However, a large cycled structure/volume change is inevitable in conversion-type or alloying-reaction anodes, which make them intrinsically unsuitable for durable sodium-ion batteries . Here, we synthesized carbon fiber-anchored vanadium nitride nanoparticles (denoted as VN@CF) through a simple molten-salt method without NH3 treatment. The VN@CF anode shows an ultra-stable Na-storage structure with a discharge capacity of 204 mAh/g at 0.1 A/g after 500 cycles. More notably, it shows remarkably long-cycling stability over 6600 cycles without capacity attenuation at 1.0 A/g. Multiple ex-situ characterizations, such as X-ray diffraction and X-ray photoelectron spectroscopy, indicate that the sodium storage behavior of VN@CF is a surface redox-related pseudocapacitive process, which is further supported by theoretical calculations. Such surface pseudocapacitive could not only enhance the sodium-storage structure stability but increase the redox reaction kinetics, which should be the origins of VN@CF's superior electrochemical properties. Our work paves a way for designing structure-stable energy storage materials based on the surface redox pseudocapacitance mechanism.
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