阳极
硫族元素
材料科学
镁
电化学
阴极
电池(电)
钝化
沉积(地质)
储能
化学工程
纳米技术
冶金
化学
电极
图层(电子)
有机化学
功率(物理)
古生物学
物理化学
工程类
物理
生物
量子力学
沉积物
作者
Liping Wang,Thomas Diemant,Zhenyou Li,Dasari Bosubabu,Zhirong Zhao‐Karger
标识
DOI:10.1021/acsaem.2c03516
摘要
Magnesium–chalcogen batteries are promising post lithium battery systems for large-scale energy storage applications in terms of energy density, material sustainability, safety, and cost. However, the soluble reaction intermediates, such as polysulfides or polyselenides, formed during the electrochemical processes can severely passivate the Mg metal anode, limiting the cycle life of the batteries. It is necessary to rescrutinize the failure in Mg–chalcogen batteries from an anodic perspective. Herein, the Mg metal anode failure mechanism is thoroughly examined, revealing that it is induced by an inhomogeneous Mg deposition promoted by soluble intermediates from chalcogen cathodes. To further confirm the mechanism and solve this anode failure problem, a multifunctional 3D current collector is used to decrease the local current density and regulate the Mg deposition behavior. The present findings are anticipated to provide guidance for anode design, enhance the life-span of Mg–chalcogen batteries, and facilitate the development of other magnesium metal batteries.
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