多硫化物
磷化物
双金属片
镍
钴
分离器(采油)
催化作用
化学工程
硫黄
无机化学
吸附
化学
材料科学
有机化学
冶金
电极
电解质
物理
物理化学
热力学
工程类
作者
Hangyi Zhu,Siyang Dong,Jing Xiong,Pengfei Wan,Xuanyang Jin,Shengjun Lu,Yufei Zhang,Haosen Fan
标识
DOI:10.1016/j.jcis.2023.03.083
摘要
Lithium-sulfur batteries (LSBs) have aroused great research interest due to their high theoretical capacity and high energy density. To further develop lithium-sulfur batteries, it has become more and more important to put more efforts in promoting the adsorption and rapid catalytic conversion of lithium polysulfides (LiPSs). Herein, Ni/Co bimetallic phosphides were encapsulated into nitrogen-doped dual carbon conductive network (NiCoP@NC) by annealing and phosphorizing Ni-ZIF-67 precursor at high temperature. Due to their numerous co-adsorption/catalytic sites and high conductivity of carbon skeleton, the encapsulated Ni/Co phosphides particles could significantly enhance the anchoring and catalytic conversion of LiPSs and provide ultrafast channels for Li+ transport. When used as a modified separator for LSBs, the cells displayed superior performance with an initial capacity of 1083.4 m Ah g-1 at 0.5 C and outstanding cycle stability with a capacity decay rate of only 0.09% per cycle for 300 cycles. Besides, even at high sulfur loading (3.2 mg cm-2), they still present satisfactory performance. Therefore, this study presents a novel strategy on how to use MOF derived bimetallic phosphides with chemical adsorption and catalytic conversion of polysulfides for high-power advanced lithium-sulfur batteries.
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