Multifunctional Self‐Assembled Bio‐Interfacial Layers for High‐Performance Zinc Metal Anodes

Author:

Lu Jiahui1ORCID,Wang Tianyi1,Yang Jian2,Shen Xin1,Pang Huan1,Sun Bing3ORCID,Wang Guoxiu3ORCID,Wang Chengyin1

Affiliation:

1. School of Chemistry and Chemical Engineering Yangzhou University 225002 Yangzhou Jiangsu Province P. R. China

2. Key Lab of Fluorine and Silicon for Energy Materials and Chemistry of Ministry of Education College of Chemistry and Chemical Engineering Jiangxi Normal University 330022 Nanchang Jiangxi Province P. R. China

3. Centre for Clean Energy Technology School of Mathematical and Physical Science Faculty of Science University of Technology Sydney 2007 Broadway NSW Australia

Abstract

AbstractRechargeable aqueous zinc‐ion (Zn‐ion) batteries are widely regarded as important candidates for next‐generation energy storage systems for low‐cost renewable energy storage. However, the development of Zn‐ion batteries is currently facing significant challenges due to uncontrollable Zn dendrite growth and severe parasitic reactions on Zn metal anodes. Herein, we report an effective strategy to improve the performance of aqueous Zn‐ion batteries by leveraging the self‐assembly of bovine serum albumin (BSA) into a bilayer configuration on Zn metal anodes. BSA′s hydrophilic and hydrophobic fragments form unique and intelligent ion channels, which regulate the migration of Zn ions and facilitate their desolvation process, significantly diminishing parasitic reactions on Zn anodes and leading to a uniform Zn deposition along the Zn (002) plane. Notably, the Zn||Zn symmetric cell with BSA as the electrolyte additive demonstrated a stable cycling performance for up to 2400 hours at a high current density of 10 mA cm−2. This work demonstrates the pivotal role of self‐assembled protein bilayer structures in improving the durability of Zn anodes in aqueous Zn‐ion batteries.

Funder

National Natural Science Foundation of China

Australian Research Council

Publisher

Wiley

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