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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Strategy of cation/anion co-doping for potential elevating of VS4 cathode for magnesium ion batteries

关键字:PERFORMANCE; NANOSHEETS; SULFIDE; POLYSULFIDES; SPECTROSCOPY; GRAPHENE; NITRIDE; STORAGE; CARBON; OXIDE

摘要:VS4 is one of the most potential cathode materials candidates for magnesium ion batteries (MIBs). However, it is still challenging for suitably modifying VS4 to make it process more excellent cycle and rate performance. Herein, modifying VS4 with cation (Mo)/anion (O) co-doping (MVSO) enhances the electrical conductivity, generates rich sulfur and oxygen vacancies, induces the co-existence of V3+/V4+ and regulates the morphology as hollow flower-like morphology. Benefitted from the advantages of co-doping of Mo and O, MVSO delivers the excellent electrochemical properties, such as the high specific capacity (140.5 mAh g(-1)) under 50 mA g(-1), ultralong cycling life about 1000 cycles with capacity retention ratio of 95.6%, superior rate capability (the capacity could achieve at 75.2 mAh g(-1), when the current density increases to 1000 mA g(-1)), and low self-discharge ratio. Furthermore, the fast reaction kinetics and high capacitive process contribution for MVSO unmasked by the galvanostatic intermittent titration technique (GITT) and pesudocapaticance-like contribution analysis are highlighted. Particularly, the intrinsic Mg2+ storage mechanism and the high reversible properties caused by MoO co-doping is unveiled with comprehensive ex situ characterizations. These findings are supposed to open new avenues for designing cathode materials for applying in future energy storage devices.

卷号:439

期号:

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