Salt‐Assisted Recovery of Sodium Metal Anodes for High‐Rate Capability Sodium Batteries
Source abstract
Abstract
Abstract Rechargeable sodium metal batteries are considered to be one of the most promising high energy density and cost‐effective electrochemical energy storage systems. However, their practicality is constrained by the high reactivity of sodium metal anodes that readily brings about excessive accumulation of inactive Na species on the surface, either by chemical reactions with oxygen and moisture during electrode handling or through electrochemical processes with electrolytes during battery operation. Herein, this paper reports on an alkali, salt‐assisted, assembly‐polymerization strategy to recover Na activity and to reinforce the solid‐electrolyte interphase (SEI) of sodium metal anodes. To achieve this, an alkali‐reactive coupling agent 3‐glycidoxypropyltrimethoxysilane (GPTMS) is applied to convert inactive Na species into Si–O–Na coordination with a self‐assembly GPTMS layer that consists of inner O–Si–O networks and outer hydrophobic epoxides. As a result, the electrochemical activity of Na metal anodes can be fully recovered and the robust GPTMS‐derived SEI layer ensures high capacity and long‐term cycling under an ultrahigh rate of 30 C (93.1 mAh g−1, 94.8% after 3000 cycles). This novel process provides surface engineering clues on designing high power density and cost‐effective alkaline metal batteries.
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Research context
OpenAlex topics: Advanced Battery Materials and Technologies · Advancements in Battery Materials · Advanced battery technologies research
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
State Key Laboratory of Powder Metallurgy Central South University Changsha Hunan 410083 P. R. China
Department of Chemical and Materials Engineering University of Alberta Edmonton Alberta T6G 1H9 Canada
Funding
National Natural Science Foundation of China · Natural Science Foundation of Hunan Province · China Postdoctoral Science Foundation
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Show source-provided references
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