Affiliation:
1. College of Chemistry and Materials Science Key Laboratory of Analytical Science and Technology of Hebei Province Institute of Life Science and Green Development Hebei University Baoding 071002 P. R. China
2. Hebei Research Center of the Basic Discipline of Synthetic Chemistry Hebei University Baoding 071002 P. R. China
Abstract
AbstractRechargeable aqueous zinc (Zn) batteries are a promising candidate for large‐scale energy storage, but the noncompact and dendritic Zn deposition, water‐induced parasitic reaction, and narrow operating temperature range severely hinder their practical application. Here, it is demonstrated that these challenges can be conquered by introducing low‐cost acetamide (Ace) into aqueous electrolytes. The non‐sacrificial Ace molecules with both donor and acceptor groups can disrupt the original H‐bonded network of water, replace the solvating‐H2O in Zn2+‐solvation sheath, form dynamic adsorption on Zn, and create an H2O‐poor electrical double‐layer. Consequently, the presence of Ace suppresses water erosion on Zn, homogenizes Zn nucleation/growth, reduces water reactivity, and depresses the freezing point of electrolyte. The formulated Ace‐containing electrolyte features a wide temperature range from −20 to 60 °C and enables highly compact and dendrite‐free Zn electrodeposition even at 25 mAh cm−2 using a non‐pressure electrolytic cell. Moreover, the Ace‐containing electrolyte allows Zn electrodes to achieve a long‐term lifespan across −20–60 °C and excellent deep cycling stability under 85.3% depth‐of‐discharge (25 mAh cm−2) with over 400 h, and supports the stable operation of Zn–Iodine full batteries under harsh conditions.
Funder
National Natural Science Foundation of China
China Association for Science and Technology
Natural Science Foundation of Hebei Province
Department of Education of Hebei Province
Subject
Electrochemistry,Condensed Matter Physics,Biomaterials,Electronic, Optical and Magnetic Materials