阳极
材料科学
储能
X射线光电子能谱
化学工程
超级电容器
钠
法拉第效率
电容器
插层(化学)
透射电子显微镜
假电容
纳米技术
电极
离子
电化学
化学
无机化学
电压
功率(物理)
电气工程
热力学
物理
物理化学
有机化学
冶金
工程类
作者
Huanyu Liang,Hao Zhang,Linyi Zhao,Zhengyuan Chen,Chuanxue Huang,Cunliang Zhang,Zhuan Liang,Yaqun Wang,Xia Wang,Qiang Li,Xiangxin Guo,Hongsen Li
标识
DOI:10.1016/j.cej.2021.131481
摘要
Abstract Sodium-ion capacitors (SICs) show great potential for large-scale energy storage devices due to their high energy-power density, long cycling life, and low cost of sodium. Nevertheless, a daunting challenge to this technology is the sluggish sodium ion diffusion kinetics of the faradaic anode materials, which impede the widespread development of SICs. Herein, uniformly layered Fe2(MoO4)3 (L-FMO) assemblies are prepared though a facile solvothermal-assisted route and used as anode material of SICs for the first time. Benefiting from the improved extrinsic pseudocapacitive contribution, the L-FMO assemblies exhibit fast kinetics, high sodium storage capacity as well as long-term lifetime. Moreover, an initial intercalation-subsequent conversion sodium storage mechanism of L-FMO assemblies is further demonstrated though a series of techniques including in-situ X-ray diffraction, ex-situ transmission electron microscopy as well as ex-situ X-ray photoelectron spectroscopy. When the L-FMO assemblies was applied into SICs, the assembled devices achieve a high-energy-power density (227.2 Wh kg−1, 20.05 kW kg−1) along with good cycling stability (a low capacity decay of only 0.0062% per cycle during 3000 cycles at the current density of 1 A g−1). The present work pioneers alkaline earth metal molybdates for SICs anodes and will push the development of energy storage systems.
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