Activation of the microstructures in nickel-based bimetallic complexes for aqueous batteries
作者机构:School of Chemistry and Chemical Engineering Yangzhou University Canadian Light Source Inc. University of Saskatchewan Center for Reliability Science and Technologies Chang Gung University Kidney Research Center Department of Nephrology Chang Gung Memorial Hospital Institute of Technology for Carbon Neutralization Yangzhou University State Key Laboratory of Coordination Chemistry Nanjing University
出 版 物:《Science China Chemistry》 (中国科学:化学(英文版))
年 卷 期:2024年
核心收录:
学科分类:0808[工学-电气工程] 081704[工学-应用化学] 07[理学] 070304[理学-物理化学(含∶化学物理)] 08[工学] 0817[工学-化学工程与技术] 0703[理学-化学]
基 金:supported by the National Natural Science Foundation of China (52371240) the Postgraduate Research & Practice Innovation Program of Jiangsu Province (KYCX23_3511)
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(NiSASSA-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-350with large specific surface area shows a higher specific capacity(0.30 mAh cm-2at 3 mA cm-2). This work hopefully provides a new perspective on the study of nanomaterial porosity in energy storage applications.