Yuxiang ChenWenning MuJunjin MengYifan HuangXiaolong BiRuimin YangXuefei LeiShaohua Luo
Supercapacitors with transition bimetallic oxides as pseudocapacitive materials have been of wide concern for their excellent energy storage performance. In this work, a simple coprecipitation method was used to synthesize the precursor, followed by calcination to prepare Ni-Cu bimetallic oxide materials. The structure, morphology and properties of the materials prepared by different precipitating agents and different calcination temperatures of NCO-H2C2O4 precursor were investigated. The optimum precipitant was determined to be H2C2O4, and Ni-Cu nanoparticles with regular lamellar microstructure were obtained at the calcination temperature of 400 °C. The nanostructure and morphology provide a large active channel for the rapid diffusion of electrolyte ions, and the specific capacitance of NCO-H2C2O4-400 electrode material can reach 740.31 F/g Cs at 1 A/g. The investigation of charge storage mechanism shows that the contribution rate of capacitance and diffusion control is about 37.9% and 67.2%, respectively. The electrochemical test results of the asymmetric supercapacitors (ASC) constructed with NCO-H2C2O4-400 and activated carbon show that the specific capacitance, energy density, and power density of the capacitor are 52.66 F/g, 16.45 Wh/kg, and 759.51 W/kg, respectively. Even after 5000 charge/discharge cycles at 5 A/g, it can still keep 90.57% of its initial capacity. This work not only provides competitive electrode materials for energy storage devices but also provides a feasible strategy for producing complex transition metal oxide materials with high capacitance performance.
Xiaohui TangBowei ZhangYu Hui LuiShan Hu
Zhang YangYanli ChenKe LiangYanrong ZhangDan WangWenchang WangJie WangNaotoshi MitsuzakiZhidong Chen
Man FengJianmin GuGuang Cong ZhangMing XuYanan YuXin LiuZhuang WangBaipeng YinYuwen LiuShimin Liu
Xianjun ZhuHuaili DaiJing HuLei DingLi Jiang
M. ManikandanE. ManikandanV SwethaS. KurpaaS. N. S. Maruthy VijayV. Kiruthika