Position difference between Mo clusters and N sites induced highly synergistic electrocatalysis in integrated electrode-separator membranes with crosslinked hierarchically porous interface

材料科学 电解质 电催化剂 电极 化学工程 分离器(采油) 电子转移 吸附 多硫化物 电化学 光化学 化学 物理化学 物理 工程类 热力学 生物化学
作者
Helong Jiang,Shenghan Gu,Jiao Guo,Yan Dai,Wenji Zheng,Xiaobin Jiang,Xuemei Wu,Wu Xiao,Gaohong He,Xiangcun Li
出处
期刊:Energy Storage Materials [Elsevier BV]
卷期号:45: 370-379 被引量:24
标识
DOI:10.1016/j.ensm.2021.12.006
摘要

Herein, scalable integrated electrode-separator membranes with hierarchical porous interface are reported for promoting Li+/electrolyte transfer and Al-free refined Li-S battery configuration. The electrode side ([email protected]) with ultrahigh porosity of 89% is composed with CNT as skeleton and Mo/N-codoped carbon (Mo-NC) as the crosslinked shell, the unique porous membrane electrode side and interface can strengthen transfer of Li+/electrons/electrolyte for fast reaction kinetics, and provide large space for polysulfide (LiPSs) anchoring and volume expansion. Furthermore, the N active sites with Li+-transfer transition function and Mo clusters with LiPSs adsorption and catalytic ability constitute a highly-efficient synergistic effect in mitigating shuttle effect and reducing energy barrier of redox reaction. For the Mo13NC-a surface with adjacent Mo and N, the LiPSs are adsorbed by Mo during the discharge process, and the N sites with lone electron pairs can accelerate diffusion of the positively charged Li+ to Mo, and to react quickly with LiPSs and transform into Li2S. For Mo13NC-b surface, however, the repulsion effect between Mo and Li+ during the charge process can promote the rapid migration of the dissociated Li+ to surround graphene due to the N center is occupied by Mo, which is beneficial to the dissociation reaction of Li2S. For the separator side ([email protected]) with CNT as the skeleton and nonconductive polymer (NP) as crosslinked shell, the porous structure also facilitates the Li+/electrolyte transport. With uniform sulfur loading in the electrode side, an Al/Cu free Li-S battery with refined configuration and long-term cycle stability is formed. The proposed strategy has an important guiding significance for the design of membrane-based electrode/separator/interlayer with low ion/electrolyte transfer resistance in Li-S batteries.
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