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室温钠硫电池阴极材料的现状与挑战

Status and Challenges of Cathode Materials for Room-Temperature Sodium-Sulfur Batteries.

作者信息

Wu Ying, Wu Liang, Wu Shufan, Yao Yu, Feng Yuezhan, Yu Yan

机构信息

Hefei National Laboratory for Physical Sciences at the Microscale Department of Materials Science and Engineering CAS Key Laboratory of Materials for Energy Conversion University of Science and Technology of China Hefei Anhui 230026 China.

Key Laboratory of Materials Processing and Mold (Zhengzhou University) Ministry of Education Zhengzhou University Zhengzhou 450002 China.

出版信息

Small Sci. 2021 Sep 24;1(11):2100059. doi: 10.1002/smsc.202100059. eCollection 2021 Nov.

Abstract

Room-temperature sodium-sulfur (RT Na-S) batteries have become the most potential large-scale energy storage systems due to the high theoretical energy density and low cost. However, the severe shuttle effect and the sluggish redox kinetics arising from the sulfur cathode cause enormous challenges for the development of RT Na-S batteries. This review systematically sheds light on the rational design strategies of integrating porous carbon matrix with "adsorption-catalysis" agents, including transition-metal single-atom, transition-metal nanoclusters, transition-metal compounds, or heterostructures. Moreover, the multistep reaction mechanism accompanied with the evolution process of various sodium polysulfides during the redox process is systematically summarized on the basis of electrochemical technique analysis and ex situ/in situ characterization. Finally, the future perspectives and potential research directions are outlined to provide a guideline for the continuous development of RT Na-S batteries.

摘要

室温钠硫(RT Na-S)电池因其高理论能量密度和低成本,已成为最具潜力的大规模储能系统。然而,硫正极产生的严重穿梭效应和缓慢的氧化还原动力学给RT Na-S电池的发展带来了巨大挑战。本文综述系统地阐述了将多孔碳基体与“吸附-催化”剂(包括过渡金属单原子、过渡金属纳米团簇、过渡金属化合物或异质结构)相结合的合理设计策略。此外,基于电化学技术分析和非原位/原位表征,系统地总结了氧化还原过程中各种多硫化钠演变过程所伴随的多步反应机理。最后,概述了未来展望和潜在的研究方向,为RT Na-S电池的持续发展提供指导。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9b81/11935918/25d54b045925/SMSC-1-2100059-g001.jpg

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