镍
锌
氢氧化物
水溶液
氢氧化锌
无机化学
金属
材料科学
金属有机骨架
金属氢氧化物
化学
冶金
有机化学
吸附
作者
Shixian Wang,Yichun Su,Zhaocheng Jiang,Zhenyang Meng,Tianyi Wang,Meifang Yang,Weijie Zhao,Han‐Yi Chen,Mohsen Shakouri,Huan Pang
出处
期刊:Nano Letters
[American Chemical Society]
日期:2024-11-14
卷期号:24 (47): 15101-15109
被引量:14
标识
DOI:10.1021/acs.nanolett.4c04414
摘要
Hydroxides exhibit a high theoretical capacity for energy storage by ion release and are often intercalated with anions to enhance the ion migration kinetics. In this study, a series of metal-hydroxide organic frameworks (MHOFs) are synthesized by intercalating aromatic organic linkers into hydroxides using I-M/Ni(OH)2 (where M = Co2+, Cu2+, Mg2+, Fe2+). The coordination environment and layer spacing (1.09 nm) of I-M/Ni(OH)2 are explored by X-ray absorption fine structure and cryo-electron microscopy. The intercalation nanostructure improves the conductivity of the hydroxides and facilitates Zn2+ migration by increasing the interlayer spacing, while enhancing the rate capability and cycling stability. Consequently, the I-Co/Ni(OH)2 material exhibites a satisfactory specific capacity of 0.35 mAh cm-2 at 3 mA cm-2 and a high peak power density of 6.78 mW cm-2. This study offers a novel perspective on the design of intercalated hydroxide and provides new insights into high-performance nickel-zinc batteres.
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