材料科学
多硫化物
钠
电解质
阳极
储能
溶解
阴极
电池(电)
分离器(采油)
化学工程
纳米技术
冶金
功率(物理)
电极
热力学
工程类
物理化学
化学
物理
标识
DOI:10.1016/j.ensm.2024.103704
摘要
Room temperature sodium-sulfur batteries (RT Na-S batteries) are regarded as promising power sources particularly for grid-scale energy storage, owing to their high theoretical capacity and low-cost electrode materials. Currently, numerous studies have focused on the S-cathode. Moreover, it is identified that the dissolution/shuttle of sodium polysulfides (NaPSs) in ether-based electrolytes and the grievous nucleophilic reaction in ester-based electrolytes are the most pivotal challenges for RT Na-S batteries. Nevertheless, the practical advancement of RT Na-S batteries is equally hampered by significant obstacles associated with Na anodes. This review starts with the discussion on the origin, cell chemistries and principles of RT Na-S batteries. Afterwards, severe challenges confronted by Na anodes especially in RT Na-S batteries are concluded. Then, we provide an exhaustive overview of the present stabilization strategies for Na anodes in polysulfides-rich environments, including electrolyte, interface and separator. Moreover, theoretical investigations to foundational data concerning stable NaPSs, surface structure, charge transfer kinetics and sodium deposition/dissolution dynamics in polysulfide-rich electrolytes are summarized. Finally, this article also provides suggestions on underscoring fundamental scientific challenges and considerations necessitating attention in order to promote comprehensive development of RT Na-S batteries.
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