材料科学
阴极
镍
化学工程
钒酸盐
阳极
氧化还原
电化学
水溶液
储能
钒
电池(电)
X射线光电子能谱
冶金
电极
化学
物理化学
工程类
功率(物理)
物理
量子力学
作者
NULL AUTHOR_ID,Quan Kuang,NULL AUTHOR_ID,NULL AUTHOR_ID,NULL AUTHOR_ID,NULL AUTHOR_ID,Youzhong Dong,NULL AUTHOR_ID
出处
期刊:Small
[Wiley]
日期:2024-07-07
标识
DOI:10.1002/smll.202404215
摘要
Abstract Aqueous nickel‐ion batteries (ANIBs) as an emerging energy storage device attracted much attention owing to their multielectron redox reaction and dendrite‐free Ni anode, yet their development is hindered by the divalent properties of Ni 2+ and the lack of suitable cathode materials. Herein, a hydrated iron vanadate (Fe 2 V 3 O 10.5 ∙1.5H 2 O, FOH) with a preferred orientation along the (200) plane is innovatively proposed and used as cathode material for ANIBs. The FOH cathode exhibits a remarkable capacity of 129.3 mAh g −1 at 50 mA g −1 and a super‐high capacity retention of 95% at 500 mA g −1 after 700 cycles. The desirable Ni 2+ storage capacity of FOH can be attributed to the preferentially oriented and tunnel structures, which offer abundant reaction active planes and a broad Ni 2+ diffusion path, the abundant vacancies and high specific surface area further increase ion storage sites and accelerate ion diffusion in the FOH lattice. Furthermore, the Ni 2+ storage mechanism and structural evolution in the FOH cathode are explored through ex situ XRD, ex situ Raman, ex situ XPS and other ex situ characteristics. This work opens a new way for designing novel cathode materials to promote the development of ANIBs.
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