多硫化物
钴
材料科学
电催化剂
氧化还原
硫黄
锂(药物)
碳纳米管
碳纤维
纳米技术
化学工程
化学
电极
冶金
复合数
电化学
复合材料
工程类
物理化学
电解质
内分泌学
医学
作者
Yiju Li,Peng Zhou,Hui Li,Tingting Gao,Lei Zhou,Yelong Zhang,Ni Xiao,Zhonghong Xia,Liang Wang,Chaoshi Ren,Lin Gu,Shaojun Guo
标识
DOI:10.1002/smtd.201900701
摘要
Abstract The development of Li‐S batteries is greatly hindered by the polysulfide shuttling and sluggish sulfur redox kinetics, leading to low utilization of active materials and rapid capacity decay. Herein, a freestanding multifunctional interlayer, prepared by layer‐by‐layer assembling of the single‐atom cobalt‐anchored nitrogen‐doped carbon nanosheets (NC@SA‐Co) and dual network of carbon nanotube‐cellulose nanofiber (CNT‐CNF) hybrid, is proposed to effectively enhance the polysulfide immobilization and sulfur redox kinetics. The conductive CNT network acts as the physical barrier to confine the polysulfide diffusion and to facilitate the reuse of polysulfides. The oxygen‐group‐terminated CNF network allows the hopping of Li + ion and suppresses the polysulfide crossover due to the strong electrostatic repulsion. Moreover, it is demonstrated that the 2D NC@SA‐Co with numerous well‐defined single sites of Co–N 4 can effectively serve as an electrocatalyst to boost the reversible reaction of polysulfides. As a result, the assembled Li‐S batteries with the multifunctional interlayer deliver a high reversible specific capacity of 1160 mAh g −1 at 0.1 C and an ultralow capacity decay of 0.058% per cycle over 700 cycles. Even with a high sulfur loading of 7.2 mg cm −2 , a high areal capacity of 8.3 mAh cm −2 can be achieved.
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