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    刘啸嵩

    • 教授 博士生导师 硕士生导师
    • 教师拼音名称:liuxiaosong
    • 电子邮箱:
    • 职务:国家同步辐射实验室副主任
    • 办公地点:安徽省合肥市蜀山区合作化南路42号中国科学技术大学国家同步辐射实验室3号楼319
    • 联系方式:0551-63602078
    • 2021年国家高层次人才特殊支持计划科技创新领军人才
    • 2020年江苏省双创团队领军人才
    • 2014年中国科学院“引进海外杰出人才(A类)”
    • 2014年上海市浦江人才

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    Highly reversible formation and decomposition of S–S dimers driven by the migration of metal Cr in layered NaCr2/3Ti1/3S2

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    DOI码:10.1038/s41467-019-12310-6

    发表刊物:Nature Communications

    关键字:X-RAY-ABSORPTION;POSITIVE ELECTRODE;CRYSTAL-STRUCTURE;VANADIUM SULFIDE;SULFUR;CHEMISTRY;CATHODES;SPECTROSCOPY;CHALLENGES;MOSSBAUER

    摘要:The use of anion redox reactions is gaining interest for increasing rechargeable capacities in alkaline ion batteries. Although anion redox coupling of S2- and (S-2)(2-) through dimerization of S-S in sulfides have been studied and reported, an anion redox process through electron hole formation has not been investigated to the best of our knowledge. Here, we report an O3-NaCr2/3Ti1/3S2 cathode that delivers a high reversible capacity of similar to 186 mAh g(-1) (0.95 Na) based on the cation and anion redox process. Various charge compensation mechanisms of the sulfur anionic redox process in layered NaCr2/3Ti1/3S2, which occur through the formation of disulfide-like species, the precipitation of elemental sulfur, S-S dimerization, and especially through the formation of electron holes, are investigated. Direct structural evidence for formation of electron holes and (S2)(n-) species with shortened S-S distances is obtained. These results provide valuable information for the development of materials based on the anionic redox reaction.

    合写作者:Guo-Xi Ren, Ji-Li Yue, Yi-Fei Mo, Xi-Qian Yu, Ming-Hui Cao, Zulipiya Shadike

    第一作者:Tian Wang

    通讯作者:Pan Liu,Xiaosong Liu,Zheng-Wen Fu

    论文编号:4458

    卷号:10

    ISSN号:2041-1723

    是否译文:

    发表时间:2019-10-01

    发布期刊链接:https://www.nature.com/articles/s41467-019-12310-6