High theoretical capacity of BiS propels it toward an ideal anode material for lithium-ion batteries (LIBs); however, rapid capacity attenuation and poor long-term stability are major barriers to widespread application. In this work, an oxygen self-doping strategy was utilized to synthesize O-BiS@C, significantly increasing the amount of active sites for lithium-ion storage. Meanwhile, sulfur vacancies were formed to improve the electrical conductivity and ionic transport efficiency, enhance the long-term stability, and accelerate the electrochemical kinetics of BiS@C. O-BSC-S1:3 anode exhibits a reversible capacity of 673.1 mAh g at 0.2 A g. It retains a long-term capacity of 596.3 mAh g over 1100 cycles at a high density of 3 A g in LIBs. Moreover, the installed O-BiS@C//LiCoO full battery offers exceptional reversible capacity and remarkable cyclability (325.2 mAh g after 200 cycles) at 0.2 A g. The combined strategy of oxygen self-doping and sulfur vacancy effectively enhances the reversible capacity and cycling life of BiS, providing an approach for the design of high-performance transition metal sulfide anodes for LIBs.
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http://dx.doi.org/10.1021/acsami.4c11172 | DOI Listing |
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