4.7 Article

Accelerating the electrochemical kinetics of metal-iodine batteries: progress and prospects

期刊

MATERIALS TODAY ENERGY
卷 30, 期 -, 页码 -

出版社

ELSEVIER SCI LTD
DOI: 10.1016/j.mtener.2022.101146

关键词

Metal iodine battery; Conversion reaction; Redox kinetics; Catalytic host; Shuttle effect; Functional interlayer

资金

  1. Natural Scientific Foundation of China [22109001]
  2. Anhui Provincial Natural Science Foundation [2108085QB58]
  3. China Postdoctoral Science Foundation [2022M713039]
  4. Anhui University
  5. Hefei National Laboratory for Physical Sciences at the Microscale [KF2020106]

向作者/读者索取更多资源

Rechargeable metal-iodine batteries have been attracting attention for their high-rate performance, remarkable energy density, and low cost, but the slow electro-chemical kinetics of iodine have hindered practical implementation. Various strategies have been explored to accelerate the redox kinetics of iodine for developing advanced metal-iodine batteries.
Rechargeable metal-iodine batteries (MIBs) have attracted tremendous attention, due to their merits of high-rate performance, remarkable energy density, and low cost. Nevertheless, the torpid electro-chemical kinetics of iodine have encumbered the development of practically implementable MIBs technology. To circumvent these issues, various strategies have been explored and utilized to accel-erate the redox kinetics of iodine species. The fundamental tuning of metal iodine redox kinetics is crucial for developing advanced and emerging MIBs. Herein, the intractable obstacles that prevent the practical implementation of MIBs are first summarized. Recent representative works of MIBs are systematically reported and discussed in terms of exploration of micro-and nanostructured iodine hosts, optimization of electrolyte formulas, modification of separators, and construction of functional interlayers. Furthermore, the construction of a catalytic iodine cathode to accelerate the real appli-cation of MIBs is proposed.(c) 2022 Elsevier Ltd. All rights reserved.

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