法拉第效率
电解质
阴极
阳极
材料科学
电化学
水溶液
吸附
化学工程
电池(电)
锌
电极
无机化学
冶金
化学
量子力学
物理
工程类
物理化学
功率(物理)
有机化学
作者
Yahui Wang,Ran Zhao,Jingjing Yang,Jiawen Zou,Anqi Zhang,Xiaomin Han,Zhifan Hu,Mengge Lv,Xinran Wang,Chuan Wu,Ying Bai
出处
期刊:Small
[Wiley]
日期:2024-10-04
标识
DOI:10.1002/smll.202406871
摘要
Abstract Aqueous zinc‐ion batteries (AZIBs) with slightly acidic electrolytes process advantages such as high safety, competitive cost, and satisfactory electrochemical performance. However, the failure behaviors of both electrodes, regarding zinc dendrite growth, interfacial parasitic reactions, and the collapse of cathode materials hinder the practical application of ZIBs. To alleviate the issues of both anode and cathode at the same time, D‐xylose (DX) is introduced to the electrolyte as a multifunctional additive. As a result, the side reaction of the anode is suppressed and the metallic deposition behavior is regulated due to the hydrogen bonding network reconstruction and preferential surface adsorption of DX; for the MnO 2 cathode, the DX adsorption can help the interfacial charge transfer and increase the reactive sites. Benefiting from these merits, DX‐optimized Zn//Zn battery displays reveal a prolonged lifespan of 6912 h and an ultra‐high cumulative capacity of 17.28 Ah cm −2 at 5 mA cm −2 . With the function of water reactivity suppression, the Coulombic efficiency reaches 99.91% at 2 mA cm −2 ; the Zn||MnO 2 full batteries exhibit excellent cyclability over 2000 cycles at 5C with an increased capacity of 118.9 mAh g −1 , indicating the dual functions to both of the electrodes for AZIBs.
科研通智能强力驱动
Strongly Powered by AbleSci AI