Electrochemical in situ construction of vanadium oxide heterostructures with boosted pseudocapacitive charge storage

被引:45
作者
Dong, Ran [1 ]
Song, Yu [1 ]
Yang, Duo [1 ]
Shi, Hua-Yu [1 ]
Qin, Zengming [1 ]
Zhang, Mingyue [1 ]
Guo, Di [1 ]
Sun, Xiaoqi [1 ]
Liu, Xiao-Xia [1 ]
机构
[1] Northeastern Univ, Dept Chem, Shenyang 110819, Peoples R China
基金
中国博士后科学基金; 中国国家自然科学基金;
关键词
MANGANESE OXIDE; RATE CAPABILITY; PERFORMANCE; SUPERCAPACITORS; CAPACITANCE; ELECTRODES;
D O I
10.1039/c9ta12097a
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Pseudocapacitive materials hold extraordinary promise for improving the energy densities of electrochemical capacitors but are often limited to electrodes with ultralow mass loadings (e.g. <1 mg cm(-2)) due to the sluggish mass transport kinetics in thicker electrodes. Here a V5O12/VO2 heterojunction nanomaterial with a built-in electric field near the heterointerface is fabricated on a 3D graphite substrate via an in situ electrochemical method for the first time, which can remarkably enhance the capacitive performance by improving the electron/ion delivery kinetics. The V5O12/VO2 electrode (mass loading similar to 10.8 mg cm(-2)) achieves a high areal capacitance of 5.03 F cm(-2) (465 F g(-1)) with a good rate capability and long cycle life, outperforming the V5O12 and VO2 counterparts, as well as the state-of-the-art reported VOX electrodes. An asymmetric supercapacitor assembled using V5O12/VO2 as the negative electrode and MnO2 as the positive electrode can deliver high areal/volumetric energy densities of 1.42 mW h cm(-2)/11.85 mW h cm(-3). An extrapolated gravimetric energy density of 18.6 W h kg(-1) can also be achieved, based on the entire weight of the device (76.6 mg cm(-2), active material ratio similar to 30%), representing a critical step of pushing pseudocapacitors toward practical applications.
引用
收藏
页码:1176 / 1183
页数:8
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