多硫化物
催化作用
化学
动力学
溶解
硫黄
氧化还原
吸附
极地的
钠
化学极性
化学工程
无机化学
纳米技术
材料科学
电极
有机化学
分子
物理化学
电解质
工程类
物理
量子力学
天文
作者
Peiyuan Wang,Shumin Sun,Xianhong Rui,Yonghui Zhang,Shiwen Wang,Yuanhua Xiao,Shao‐Ming Fang,Yan Yu
标识
DOI:10.1002/smtd.202201728
摘要
Abstract Due to the high theoretical energy density, low cost, and rich abundance of sodium and sulfur, room‐temperature sodium–sulfur (RT Na–S) batteries are investigated as the promising energy storage system. However, the inherent insulation of the S 8 , the dissolution and shuttle of the intermediate sodium polysulfides (NaPSs), and especially the sluggish conversion kinetics, restrict the commercial application of the RT Na–S batteries. To address these issues, various catalysts are developed to immobilize the soluble NaPSs and accelerate the conversion kinetics. Among them, the polar catalysts display impressive performance. Polar catalysts not only can significantly accelerate (or alter) the redox process, but also can adsorb polar NaPSs through polar–polar interaction because of their intrinsic polarity, thus inhibiting the notorious shuttle effect. Herein, the recent advances in the electrocatalytic effect of polar catalysts on the manipulation of S speciation pathways in RT Na–S batteries are reviewed. Furthermore, challenges and research directions to realize rapid and reversible sulfur conversion are put forward to promote the practical application of RT Na–S batteries.
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