Jiaying Zhang, Tingyang Xie, Minying Zhao, Yiqing Liu, Nguyen Duc Hoa, Alice A. Kasera, Ronghua Zeng, Guozheng Ma, Yuhong Luo, Yongbo Wu, Xiaoming Lin
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引用次数: 0
Abstract
Transition metal oxides with low cost and good redox properties are excellent candidates for supercapacitor electrode materials. Herein, we present the synthesis of MOF-derived dual transition metal oxide heterojunction nanostructures (NiO/V2O3/C) via hydrothermal and thermal processes. The influence of different ligands and thermal conditions on the electrochemical performance of the resulting materials was systematically examined. The NiO/V2O3/C (NVI-500) electrode material, comprising isonicotinic acid as a ligand, exhibits distinctive heterojunction characteristics at the nanoparticle interfaces, a substantial specific surface area, and synergistic effects that collectively contribute to an exceptional specific capacitance of up to 855 F g-1 at 1 A g-1. Encouragingly, the capacity conservation rate of NVI-500 is 68.1% after 3000 cycles (10 A g-1). Furthermore, the constructed asymmetric supercapacitors demonstrated excellent energy density (26.6 Wh kg-1) and power density (400 W kg-1) with an initial capacitance retention of 83.8% after 9000 cycles. This finding serves to demonstrate that the construction of non-homogeneous transition metal oxides using MOFs as precursors is indeed a feasible strategy.
过渡金属氧化物具有低廉的成本和良好的氧化还原性能,是超级电容器电极材料的理想选择。本文采用水热法和热法合成了mof衍生的双过渡金属氧化物异质结纳米结构(NiO/V2O3/C)。系统地考察了不同配体和热条件对合成材料电化学性能的影响。由异烟酸作为配体组成的NiO/V2O3/C (NVI-500)电极材料在纳米颗粒界面处表现出独特的异质结特性,具有相当大的比表面积和协同效应,共同有助于在1 a g-1时达到855 F -1的特殊比电容。令人鼓舞的是,经过3000次循环(10 A g-1), NVI-500的容量节约率为68.1%。此外,所构建的非对称超级电容器在9000次循环后具有良好的能量密度(26.6 Wh kg-1)和功率密度(400 W kg-1),初始电容保持率为83.8%。这一发现表明,利用mof作为前体构建非均相过渡金属氧化物确实是一种可行的策略。
期刊介绍:
Electrochimica Acta is an international journal. It is intended for the publication of both original work and reviews in the field of electrochemistry. Electrochemistry should be interpreted to mean any of the research fields covered by the Divisions of the International Society of Electrochemistry listed below, as well as emerging scientific domains covered by ISE New Topics Committee.