多硫化物
兴奋剂
杂原子
电化学
掺杂剂
吸附
催化作用
热液循环
阴极
材料科学
化学工程
石墨烯
多孔性
纳米材料
化学
纳米技术
电解质
光电子学
电极
复合材料
物理化学
有机化学
工程类
戒指(化学)
作者
Weiwei Jiang,Yahui Li,Junjie Li,Guoyu Ding,Yijie Zhan,Jiajia Peng,Xiaofei Yan,Xi Deng,Jiawei Tan,Jiawei Xu,Changxin Tang,Yu Dai,Fugen Sun
标识
DOI:10.1016/j.jallcom.2023.168880
摘要
The oxygen doped MoS2 nanosheets were in-situ grown into the three-dimensional (3D) porous graphene frameworks (O-MoS2/G) through a facile hydrothermal method, and then used to coat the commercial PP separators for Li-S batteries. The relatively low hydrothermal temperature should be a key factor for achieving the O-doped MoS2. The O dopants could expand and disturb interlayer structures of MoS2 to produce abundant active edge sites for adsorption and catalytic conversion of polysulfides. Moreover, the basal planes of MoS2 should be also activated by the O doping and exhibit enhanced chemical adsorption strength towards polysulfides for propelling electrochemical conversion. Owing to the synergistic effects of the 3D porous graphene frameworks and the inlaid O-MoS2 nanosheets, the Li-S cells with high S areal loading cathodes and O-MoS2/[email protected] separators exhibit excellent electrochemical performances with a high specific capacity of 1141 mAh g−1 at the 1st cycle at 0.1 C, reversible capacities of 772 mAh g−1 at the 50th cycle at 0.2 C and 583 mAh g−1 at the 100th cycle at 0.5 C. These encouraging results provide that the heteroatom doping should be a promising approach to improve the adsorption and catalytic activity of MoS2 for propelling the polysulfide conversion in Li-S batteries.
科研通智能强力驱动
Strongly Powered by AbleSci AI