Supernormal Conversion Anode Consisting of High-Density MoS₂ Bubbles Wrapped in Thin Carbon Network by Self-Sulfuration of Polyoxometalate Complex.

Abstract

Large-capacity conversion electrodes are highly required to raise the energy density of batteries. However, their undesired phase segregation and volume expansion during cycling lead to the motivation for nanofabrication and nanochemistry of active species in order to decrease "dead mass" and promote better construction of conductive networks. However, the inactivity of the conductive skeleton and loose nanostructure would compromise the energy density of the electrode. The integration of large-sized (high-density) grains into an electroactive conductive network in a compact way is still a big challenge. Here we report a proof-of-concept prototype consisting of unusual MoS₂ solid bubbles of hundreds of nanometers in size, which are conformally encapsulated by thin-layer carbon. The seamless welding between this carbon coating and the surrounding broader carbon substrate can effectively avoid the peel-off of active species and breakage of the conductive network. This MoS₂-C composite is achieved by simultaneous self-sulfuration and self-carbonization of a polyoxometalate (POM)-based chelate, and its Li-storage performance is superior to most MoS₂-based anodes even with ultrathin 2D nanosheets. Partially benefiting from the electroactivity of a dithiooxamide (DTO)-derivate carbon network, the reversible capacity of MoS₂-C by pyrolyzing the POM-DTO chelate can reach 1500-2000 mAh/g at 0.5-1 A/g even after 700 cycles and be maintained around 1000 mAh/g under as high as 10-20 A/g.