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.