材料科学
纳米团簇
电化学
阴极
钒
氧化钒
电池(电)
氧化物
电解质
储能
介电谱
纳米技术
离子
化学工程
无机化学
电极
物理化学
冶金
化学
有机化学
功率(物理)
工程类
物理
量子力学
作者
Yingwen Cheng,Yuyan Shao,V. Bheema Raju,Xiulei Ji,B. Layla Mehdi,Kee Sung Han,Mark H. Engelhard,Guosheng Li,Nigel D. Browning,Karl T. Mueller,Jun Li
标识
DOI:10.1002/adfm.201505501
摘要
Mg batteries have potential advantages in terms of safety, cost, and reliability over existing battery technologies, but their practical implementations are hindered by the lack of amenable high-voltage cathode materials. The development of cathode materials is complicated by limited understandings of the unique divalent Mg2+ ion electrochemistry and the interaction/transportation of Mg2+ ions with host materials. Here, it is shown that highly dispersed vanadium oxide (V2O5) nanoclusters supported on porous carbon frameworks are able to react with Mg2+ ions reversibly in electrolytes that are compatible with Mg metal, and exhibit high capacities and good reaction kinetics. They are able to deliver initial capacities exceeding 300 mAh g−1 at 40 mA g−1 in the voltage window of 0.5 to 2.8 V. The combined electron microscope, spectroscopy, and electrochemistry characterizations suggest a surface-controlled pseudocapacitive electrochemical reaction, and may be best described as a molecular energy storage mechanism. This work can provide a new approach of using the molecular mechanism for pseudocapacitive storage of Mg2+ for Mg batteries cathode materials.
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