Yang Yuan, Wang Xiuqin, Huang Feifei, Zhao Jialu, Wang Xiuhua
College of Chemistry and Materials Science, Anhui Normal University, The Key Laboratory of Functional Molecular Solids, Ministry of Education, Anhui Laboratory of Molecular-Based Materials, The Key Laboratory of Electrochemical Clean Energy of Anhui Higher Education Institutes, Wuhu 241002, China.
Dalton Trans. 2020 Dec 15;49(47):17310-17320. doi: 10.1039/d0dt03237a.
A novel Co-Co LDH/C/Ni(OH)2 nanostructure was constructed by loading Ni(OH)2 nanodots on hollow Co-Co LDH/C nanocages derived from MOFs. The Co-Co LDH/C/Ni(OH)2 nanostructure revealed a high specific capacitance of up to 1426 F g-1 at 1 A g-1 and an outstanding rate capability with 90.2% retention at 10 A g-1 owing to the cooperative effect of the Ni(OH)2 nanodots and hollow Co-Co LDH/C nanocages. The electrochemical kinetic analysis showed that the Co-Co LDH/C/Ni(OH)2 electrode was dominated by surface capacitance control, demonstrating the origins of performance improvement. This work may provide an effective strategy by combining nanodots with hollow porous structures for low-cost and efficient energy storage materials.
通过将氢氧化镍纳米点负载在由金属有机框架衍生而来的中空钴-钴层状双氢氧化物/碳纳米笼上,构建了一种新型的钴-钴层状双氢氧化物/碳/氢氧化镍纳米结构。由于氢氧化镍纳米点与中空钴-钴层状双氢氧化物/碳纳米笼的协同效应,钴-钴层状双氢氧化物/碳/氢氧化镍纳米结构在1 A g-1时显示出高达1426 F g-1的高比电容以及出色的倍率性能,在10 A g-1时电容保持率为90.2%。电化学动力学分析表明,钴-钴层状双氢氧化物/碳/氢氧化镍电极受表面电容控制,这证明了性能提升的根源。这项工作可能通过将纳米点与中空多孔结构相结合,为低成本、高效储能材料提供一种有效的策略。