青岛科技大学  English 
李桂村
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教授 博士生导师  
硕士生导师  

教师拼音名称:liguicun

出生日期:1974-05-12

电子邮箱:

所在单位:材料学院综合办公室

职务:材料科学与工程学院院长

学历:博士研究生

办公地点:材料楼225房间

性别:男

联系方式:guicunli@qust.edu.cn Tel:13730918070

学位:工学博士

职称:教授

毕业院校:中国海洋大学

学科:

材料物理与化学

曾获荣誉:

2016-01-01 山东省有突出贡献的中青年专家

2012-11-07 山东省第三届优秀研究生指导教师

2011-04-01 青岛拔尖人才

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Study on synergy effect of hydrated ionic radius and oxidation state for pre-intercalated cations towards highly reversible magnesium ions batteries

关键字:STORAGE; VS4; FILMS

摘要:Magnesium ions batteries (MIBs) are promising in that Mg anode shows high theoretical volumetric capacity (3833 mAh cm-3) and is dendrite free deposition upon charging. However, the higher charge/radius ratio of Mg2 with bivalent nature shows strong electrostatic interaction between Mg2 and host anion lattice of VS4 in situ grown on N doped tubular graphene (VS4/N-TG), causing the sluggish reaction kinetics and poorer structural stability. Therefore, there is great need to develop strategy for modifying VS4/N-TG. Although interlayer preintercalation is an effective way to improve the overall cell performance, the systematic study about the ious ionic radius and oxidation states of pre-intercalated cations on modulating electronic structure to enhance the electrochemical performance has not been focused. In this study, cations pre-intercalation engineering is achieved in VS4/N-TG for constructing M0.06VS4/N-TG cathode via electrochemical method. After the systematic study about the effect of hydrated ionic radius and oxidation state of ious pre-intercalated cations on electrochemical performance of M0.06VS4/N-TG, pre-intercalated Mg2 with moderate hydrated ionic radius and oxidation state would enlarge the interchain spacing for facilitating magnesium working ions transportation and maintaining structural stability, as well as change the oxidation states of V element as V2 and V3 to enhance the electrochemical reactivity. Therefore, Mg0.06VS4/N-TG deliver superior electrochemical properties, including the excellent cycling stability with nearly 100% capacity retention ratio after 1500 cycles, high specific capacity about 170 mAh/g at 50 mA g-1, superior rate capability (107 mAh/g at 1000 mA g-1) and high antiself-discharge behavior. The highlighted synergic effect of the hydrated ionic radius and oxidation state would guide more energy storage devices design for obtaining the excellent electrochemical performance.

卷号:471

期号:-

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