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
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
最后更新时间:..
关键字:N-TG;Mo-doped VS4;rich sulfur vacancies;cathode materials;Mg-ion batteries
摘要:The development of cathode materials with a high electric conductivity and a low polarization effect is crucial for enhancing the electrochemical properties of magnesium-ion batteries (MIBs). Herein, Mo doping and nitrogen-doped tubular graphene (N-TG) introduction are carried out for decorating VS4 (Mo-VS4/N-TG) via the one-step hydrothermal method as a freestanding cathode for MIBs. The results of characterizations and density functional theory (DFT) reveal that rich sulfur vacancies are induced by Mo doping, and N-TG as a high conductive skeleton material serves to disperse the active material and forms a tight connection, all of which collectively improved the electrical conductivity of electrode and increased the adsorption energy of Mg2+ (-6.341 eV). Furthermore, the fast reaction kinetics is also confirmed by the galvanostatic intermittent titration technique (GITT) and the pesudocapacitance-like contribution analysis. Benefiting from the synergistic effect of electrical conductivity enhancement and rich vacancy introduction, Mo-VS4/N-TG delivers a steady Mg2+ storage specific capacity of about 140 mAh g(-1) at 50 mA g(-1) outstanding cycle stability (80.6% capacity retention ratio after 1200 cycles under 500 mA g(-1)), and excellent rate capability (specific capacity reaches 77.1 mAh g(-1) when the current density reaches 500 mA g(-1)). In addition, the reversible reaction process, intercalation mechanism, and structural stability during the Mg2+ insertion/extraction process are confirmed by a series of ex situ characterizations. This research provides a sustainable and scalable strategy to spur the development of MIBs.
卷号:13
期号:45
是否译文:否