多硫化物
电化学
材料科学
锂硫电池
催化作用
串联
化学工程
异质结
锂(药物)
硫黄
无机化学
电极
纳米技术
化学
复合材料
电解质
光电子学
物理化学
有机化学
医学
工程类
冶金
内分泌学
作者
Ni Wang,Wenbin Li,Guiqiang Cao,Ruixian Duan,Jingjie Pei,Penghui Luo,Jianhua Zhang,Jingjing Wang,Xifei Li
标识
DOI:10.1016/j.jallcom.2023.173394
摘要
The “shuttle effect” caused by polysulfide (LiPSs) dissolution and diffusion is a great challenge for sulfur (S) cathode in lithium-sulfur batteries (LSBs). Herein, we have successfully constructed Co/CoV2O6 tandem catalytic heterostructure anchored by N-doped carbon (Co/CoV2O6/NC) via an impregnation-assisted pyriaolysis method. The “adsorption-transfer-conversion” tandem catalytic mechanism for LiPSs is realized by utilizing the three behaviors of the strong chemical adsorption of CoV2O6 to LiPSs, the strong conversion of Co to LiPSs, and the transport effect of CoV2O6←Co interfacial built-in electric field to polysulfide ions. This can effectively suppress the “shuttle effect” by separating the adsorption and conversion process of LiPSs at different active sites. The tandem catalytic characteristic coupled with the interfacial Co-N and V-N bonds among Co, CoV2O6 and NC, the high electrical conductivities of metal Co and NC conducting network, the hierarchical porous structure of polyhedral framework, collectively endow Co/CoV2O6/NC@S cathode with strong structural stability, weak electrochemical polarization, good electrochemical reversibility and fast electrochemical kinetics. As a result, Co/CoV2O6/NC@S cathode presents the significantly enhanced electrochemical performance with a high capacity of 558.4 mAh g-1 at 0.2 C after 100 cycles and a low-capacity decay rate of 0.123% per cycle during 300 cycles at 1 C.
科研通智能强力驱动
Strongly Powered by AbleSci AI