Activation of the microstructures in nickel-based bimetallic complexes for aqueous batteries

被引:1
|
作者
Su, Yichun [1 ]
Zhang, Yanfei [1 ]
Yuan, Guoqiang [1 ]
Tang, Yijian [1 ]
Zhang, Guangxun [1 ]
Shakouri, Mohsen [2 ]
Chen, Hsiao-Chien [3 ,4 ]
Zhou, Huijie [5 ]
Liu, Zheng [1 ]
Pang, Huan [1 ,6 ]
机构
[1] Yangzhou Univ, Sch Chem & Chem Engn, Yangzhou 225002, Peoples R China
[2] Univ Saskatchewan, Canadian Light Source Inc, Saskatoon, SK S7N 2V3, Canada
[3] Chang Gung Univ, Ctr Reliabil Sci & Technol, Taoyuan 333, Peoples R China
[4] Chang Gung Mem Hosp, Kidney Res Ctr, Dept Nephrol, Taoyuan 333, Peoples R China
[5] Yangzhou Univ, Inst Technol Carbon Neutralizat, Yangzhou 225002, Peoples R China
[6] Nanjing Univ, State Key Lab Coordinat Chem, Nanjing 210023, Peoples R China
来源
基金
中国国家自然科学基金;
关键词
thermal activation; mesoporous microstructure; ligand competition; nickel-based complexes; aqueous batteries; HIGH-PERFORMANCE; METAL; MOF; ZN; ADSORPTION; NI;
D O I
10.1007/s11426-024-2374-0
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The full utilization of active metal sites is meaningful for enhancing the application of materials in the energy storage field. In this study, a nickel-based nanosphere (NiSA-SSA-Co) precursor was obtained via effective doping based on a dual-ligand complex. With thermal activation, the pore microstructure of the precursor was modulated, and a transition state complex (NiSA-SSA-Co-350) was fabricated. NiSA-SSA-Co-350 not only retains part of the framework structure, but also fully exposes the metal nodes and enhances the efficiency of the active sites. NiSA-SSA-Co-350 exhibits optimal conductivity and intrinsic reactivity when applied as an electrode material for nickel-zinc batteries (NZBs). In contrast to the precursor, NiSA-SSA-Co-350 with large specific surface area shows a higher specific capacity (0.30 mAh cm-2 at 3 mA cm-2). This work hopefully provides a new perspective on the study of nanomaterial porosity in energy storage applications.
引用
收藏
页数:9
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