Polycation‐Regulated Electrolyte and Interfacial Electric Fields for Stable Zinc Metal Batteries

Author:

Peng Mengke1,Tang Xiannong1,Xiao Kang2,Hu Ting2,Yuan Kai1,Chen Yiwang13ORCID

Affiliation:

1. College of Chemistry and Chemical Engineering/Institute of Polymers and Energy Chemistry (IPEC)/Jiangxi Provincial Key Laboratory of New Energy Chemistry Nanchang University 999 Xuefu Avenue Nanchang 330031 China

2. School of Physics and Materials Science Nanchang University 999 Xuefu Avenue Nanchang 330031 China

3. National Engineering Research Center for Carbohydrate Synthesis Key Laboratory of Fluorine and Silicon for Energy Materials and Chemistry of Ministry of Education Jiangxi Normal University 99 Ziyang Avenue Nanchang 330022 China

Abstract

AbstractZn metal as one of promising anode materials for aqueous batteries but suffers from disreputable dendrite growth, grievous hydrogen evolution and corrosion. Here, a polycation additive, polydiallyl dimethylammonium chloride (PDD), is introduced to achieve long‐term and highly reversible Zn plating/stripping. Specifically, the PDD can simultaneously regulate the electric fields of electrolyte and Zn/electrolyte interface to improve Zn2+ migration behaviors and guide dominant Zn (002) deposition, which is veritably detected by Zeta potential, Kelvin probe force microscopy and scanning electrochemical microscopy. Moreover, PDD also creates a positive charge‐rich protective outer layer and a N‐rich hybrid inner layer, which accelerates the Zn2+ desolvation during plating process and blocks the direct contact between water molecules and Zn anode. Thereby, the reversibility and long‐term stability of Zn anodes are substantially improved, as certified by a higher average coulombic efficiency of 99.7 % for Zn||Cu cells and 22 times longer life for Zn||Zn cells compared with that of PDD‐free electrolyte.

Funder

National Natural Science Foundation of China

Publisher

Wiley

Subject

General Chemistry,Catalysis

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