电解质
材料科学
阴极
电化学
阳极
溶解
共晶体系
化学工程
水溶液
成核
电池(电)
无机化学
电极
冶金
化学
合金
物理化学
有机化学
热力学
功率(物理)
工程类
物理
作者
Prakas Samanta,Souvik Ghosh,Aniruddha Kundu,Haradhan Kolya,Chun–Won Kang,Pranab Samanta,Naresh Chandra Murmu,Tapas Kuila
出处
期刊:ACS Sustainable Chemistry & Engineering
[American Chemical Society]
日期:2023-03-29
卷期号:11 (14): 5495-5505
被引量:6
标识
DOI:10.1021/acssuschemeng.2c07125
摘要
Aqueous rechargeable Zn-ion batteries (ZiBs) are receiving increasing attention worldwide owing to their inherent safety and cost effectiveness. However, ZiBs are still struggling with rapid performance degradation caused by poor Zn anode reversibility and cathode dissolution into aqueous electrolytes. Inspired by the knowledge of industrial-scale Zn electroplating, a cyanide functional group containing a succinonitrile (SN) neutral ligand-based hydrated eutectic electrolyte was used to mitigate these issues. The ligand-oriented SN partially replaced free water molecules from the Zn2+ ion primary solvation sheath, resulting in delayed oxidation and a smaller Zn2+ ion desolvation energy barrier which promoted uniform Zn nucleation. Moreover, the MoO3@Mn3O4 cathode and Zn anode-based ZiB in an eutectic hydrated electrolyte with a 10:10 molar ratio of ZnCl2 and SN exhibited an ∼2.3 V working potential window which delivered a maximum of ∼476 mAh g–1 specific capacity and ∼232.2 Wh kg–1 energy density at a 0.2 A g–1 current density. The fabricated device exhibited ∼79.56% specific capacity retention after 5000 cycles at a 10 A g–1 current density. The coinsertion/extraction of H+ and Zn2+ ions and the Zn deposition/dissolution mechanism of the optimized hydrated eutectic electrolyte-based ZiBs are investigated by ex situ physicochemical and electrochemical studies. Overall, this work provides a new path on exploring green electrolytes and layered-structure materials for the development of high-performance ZiBs.
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