Affiliation:
1. College of Chemistry and Chemical Engineering State Key Laboratory of Advanced Chemical Power Sources (SKL‐ACPS) College of Materials Science and Engineering National Innovation Center for Industry‐Education Integration of Energy Storage Technology Chongqing University Chongqing 400044 China
2. College of Chemistry and Chemical Engineering State Key Laboratory of Advanced Chemical Power Sources (SKL‐ACPS) Chongqing University Chongqing 400044 China
Abstract
AbstractZinc metal has emerged as a promising candidate for high‐capacity and low‐cost anodes in aqueous zinc‐ion batteries; nevertheless, it encounters serious obstacles, including low cycling stability and poor reversibility, caused by parasitic reactions and the formation of zinc dendrites. Herein, the study proposes a novel nonprotonic dimethylacetamide (DMAC)/ZnCl2/LiCl electrolyte that enables both solvation structural modulation of [ZnClx]2‐x and the cationic electrostatic shielding effect of [Li(DMAC)]+ by controlling the concentration of LiCl. The optimal concentration of LiCl electrolyte (0.28 m), which results in the highest ratio of [ZnCl3]−, strikes a balance between low desolvation energy and a high mass transfer rate while promoting homoepitaxial deposition of Zn (002). Moreover, inert [Li(DMAC)]+ ions, which possess a lower reduction potential, preferentially adsorb onto zinc protrusions, mitigating the tip effect. Leveraging electrolyte engineering, the zinc deposition/stripping process results in impressive long‐term stability, surpassing 2,800 cycles, and the Zn||MnO2 cell also achieves a stable lifespan extending beyond 1400 cycles. The research highlights the potential of LiCl as an additive in the modulation of water‐free electrolytes.
Funder
National Key Research and Development Program of China
National Natural Science Foundation of China