淡江大學機構典藏:Item 987654321/120720
English  |  正體中文  |  简体中文  |  全文笔数/总笔数 : 64198/96992 (66%)
造访人次 : 7984234      在线人数 : 8177
RC Version 7.0 © Powered By DSPACE, MIT. Enhanced by NTU Library & TKU Library IR team.
搜寻范围 查询小技巧:
  • 您可在西文检索词汇前后加上"双引号",以获取较精准的检索结果
  • 若欲以作者姓名搜寻,建议至进阶搜寻限定作者字段,可获得较完整数据
  • 进阶搜寻


    jsp.display-item.identifier=請使用永久網址來引用或連結此文件: https://tkuir.lib.tku.edu.tw/dspace/handle/987654321/120720


    题名: Critical Factors Controlling Superoxide Reactions in Lithium-Oxygen Batteries
    作者: Wang, Y.;Lu, Y. R.;Dong, C. L.;Lu, Y. C.
    日期: 2020-03-27
    上传时间: 2021-05-05 12:12:06 (UTC+8)
    摘要: Superoxide (LiO2) formation on charging is one of the major causes of poor cycle life of Li–O2 batteries. The underlying mechanism controlling LiO2 formation remains elusive. Here, we reveal that the formation of LiO2 is mainly controlled by oxidation potential and solvent donicity, which regulates the rates of LiO2 formation and consumption via electrochemical oxidation and disproportionation. We quantify LiO2 in the electrolyte under a wide range of charging potentials via rotating-ring disk chronoamperometry and reveal that the amount of LiO2 decreases with increasing charging potential and decreasing solvent donicity. X-ray absorption near-edge structure spectroscopy results support the formation of LiO2 at low charge potentials. Li2CO3 is observed along with LiO2 formation, indicating severe side reactions resulting from LiO2. Our study reveals the underlying mechanism controlling LiO2 formation on charging Li–O2 batteries and highlights that strategies which simultaneously reduce charge potential and bypass LiO2 (e.g., redox mediator) should be developed to enable efficient and reversible Li–O2 batteries.
    關聯: ACS Energy Letters 5(5), p.1355–1363
    DOI: 10.1021/acsenergylett.0c00365
    显示于类别:[電機工程學系暨研究所] 期刊論文

    文件中的档案:

    档案 描述 大小格式浏览次数
    Critical Factors Controlling Superoxide Reactions in Lithium-Oxygen Batteries.pdf4476KbAdobe PDF4检视/开启
    index.html0KbHTML130检视/开启

    在機構典藏中所有的数据项都受到原著作权保护.

    TAIR相关文章

    DSpace Software Copyright © 2002-2004  MIT &  Hewlett-Packard  /   Enhanced by   NTU Library & TKU Library IR teams. Copyright ©   - 回馈