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非水可充电电池中的碱金属和碱土金属离子-溶剂共嵌入反应。

Alkali and alkaline-earth metal ion-solvent co-intercalation reactions in nonaqueous rechargeable batteries.

作者信息

Li Lin, Hu Zhe, Zhao Shuo, Chou Shu-Lei

机构信息

Institute for Carbon Neutralization, College of Chemistry and Materials Engineering, Wenzhou University Wenzhou Zhejiang 325035 China

Key Laboratory of Advanced Energy Materials Chemistry, Ministry of Education, Renewable Energy Conversion and Storage Center, College of Chemistry, Nankai University Tianjin 300071 China.

出版信息

Chem Sci. 2021 Nov 12;12(46):15206-15218. doi: 10.1039/d1sc04202e. eCollection 2021 Dec 1.

Abstract

Alkali and alkaline-earth metal ion-solvent co-intercalation reactions have attracted extensive attention in recent years owing to the advantage of the absence of a desolvation process, which generally results in fast kinetics and good rate performance for batteries. However, less attention has been paid to summarizing the mechanism, performance and other related aspects about ion-solvent co-intercalation reaction in batteries. A summary of alkali and alkaline-earth metal ion-solvent co-intercalation reactions in nonaqueous rechargeable batteries is presented in this review, which mainly focuses on the electrochemical performance, ion-solvent co-intercalation mechanism, conditions for reversible ion-solvent co-intercalation and potential for practical application. It is suggested that future research should focus on reducing the redox potential of the ion-solvent co-intercalation reaction to achieve high energy-density and power-density full cells. This review provides an understanding of alkali and alkaline-earth metal ion-solvent co-intercalation reactions in nonaqueous rechargeable batteries and will serve as significant guidance for researchers to further develop ion-solvent co-intercalation reactions for fast-charging batteries.

摘要

近年来,碱金属和碱土金属离子 - 溶剂共嵌入反应因其不存在去溶剂化过程的优势而备受关注,这通常会使电池具有快速动力学和良好的倍率性能。然而,关于电池中离子 - 溶剂共嵌入反应的机理、性能及其他相关方面的总结却较少受到关注。本文综述了非水可充电电池中的碱金属和碱土金属离子 - 溶剂共嵌入反应,主要聚焦于其电化学性能、离子 - 溶剂共嵌入机理、可逆离子 - 溶剂共嵌入的条件以及实际应用潜力。建议未来的研究应集中在降低离子 - 溶剂共嵌入反应的氧化还原电位,以实现高能量密度和功率密度的全电池。本综述有助于理解非水可充电电池中的碱金属和碱土金属离子 - 溶剂共嵌入反应,并将为研究人员进一步开发用于快速充电电池的离子 - 溶剂共嵌入反应提供重要指导。

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