期刊
JOURNAL OF ALLOYS AND COMPOUNDS
卷 896, 期 -, 页码 -出版社
ELSEVIER SCIENCE SA
DOI: 10.1016/j.jallcom.2021.163071
关键词
AZIBs; Cathode material; V2O5 nanofibers; Zn-storage
资金
- Scientific and Technological Innovation Foundation of Shunde Graduate School, USTB [BK21BE010]
- Guangdong Science and Technology Major Special Fund [2019-252]
Aqueous zinc-ion batteries (AZIBs) are being vigorously explored as a novel and competitive candidate for large-scale energy storage, with high safety, eco-friendliness, and low cost. Efficient Zn-storage with desirable cycling stability and rate capability can be achieved by constructing suitable cathode materials and fast Zn2+ diffusion kinetics. The novel V2O5 nanofibers show promising specific capacity and rate capability when used as a cathode material for AZIBs, matching with aqueous Zn(CF3SO3)2 electrolyte.
Aqueous zinc-ion batteries (AZIBs) are now vigorously explored as a class of novel and competitive candidates for large-scale energy storage in terms of high safety, eco-friendliness and low cost. In order to realize efficient Zn-storage with desirable cycling stability and rate capability, constructing suitable cathode materials that possess reliable host structure and fast Zn2+ diffusion kinetics makes a lot of sense. Herein, novel V2O5 nanofibers were facilely synthesized via a hydrothermal method and employed as a cathode material for AZIBs. By matching with aqueous Zn(CF3SO3)2 electrolyte, the cathode is able to achieve a specific capacity as high as 264.5 mAh g-1 at 200 mA g-1. Even conducted at a large current density of 2000 mA g-1, a considerable rate capability of 132.6 mAh g-1 can also be delivered. In addition, electrochemical reaction kinetics and ion diffusion mechanism were initially conducted to uncover the insights for efficient Zn-storage. This work is anticipated to offer feasible strategy for the design and fabrication of promising vanadium-based cathode materials for rechargeable AZIBs. (c) 2021 Elsevier B.V. All rights reserved.
作者
我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。
推荐
暂无数据