Huang Xiang-Long, Li Xue, Yang Mingyue, Yang Yeqing, Qian Jiahao, Yao Long, Zhu Kunjie, Liu Hua-Kun, Wang Yun-Xiao
Institute of Energy Materials Science (IEMS), University of Shanghai for Science and Technology, Shanghai 200093, China.
School of Physics, University of Electronic Science and Technology of China, Chengdu 611731, China.
Chem Commun (Camb). 2025 Jan 30;61(11):2156-2172. doi: 10.1039/d4cc06120a.
Room-temperature sodium-sulfur (RT Na-S) batteries that typically feature multielectron conversion chemistries can allow an ultrahigh specific capacity of 1675 mA h g and a high energy density of 1275 W h kg but unfortunately suffer from a lot of intractable challenges from sulfur cathodes. These issues cover the poor electronic conductivity of pristine sulfur and solid products, the severe shuttle effect of polysulfides, and the sluggish redox kinetics, The shuttling behavior of polysulfides always leads to cathode/anode instability and performance degeneration. Recently, the emerging catalysis strategy has been demonstrated as a reliable pathway to tackle the central issues caused by sulfur electrochemistry and revitalize RT Na-S batteries. This review provides an overview of electrocatalysis in the realm of RT Na-S batteries. Sulfur conversion chemistries and critical challenges in RT Na-S batteries are generalized firstly. The emphasis is focused on discussing chemisorption mechanisms for polysulfides, material innovation of catalysts, selectivity and design of catalysts, and a series of catalysis regulation strategies. Finally, existing challenges and perspectives regarding catalysis in RT Na-S batteries are offered, with the aim of propelling its rapid development.
室温钠硫(RT Na-S)电池通常具有多电子转换化学特性,可实现1675 mA h g的超高比容量和1275 W h kg的高能量密度,但不幸的是,硫阴极面临诸多棘手挑战。这些问题包括原始硫和固体产物的电子导电性差、多硫化物的严重穿梭效应以及缓慢的氧化还原动力学。多硫化物的穿梭行为总是导致阴极/阳极不稳定和性能退化。最近,新兴的催化策略已被证明是解决硫电化学引起的核心问题并振兴室温钠硫电池的可靠途径。本文综述了室温钠硫电池领域的电催化。首先概述了室温钠硫电池中的硫转化化学和关键挑战。重点讨论了多硫化物的化学吸附机制、催化剂的材料创新、催化剂的选择性和设计以及一系列催化调控策略。最后,针对室温钠硫电池催化提出了现有挑战和展望,旨在推动其快速发展。