Synergistic effects of nanocarbon spheres sheathed on a binderless CoMoO4 electrode for high-performance asymmetric supercapacitor

被引:29
作者
Bhattarai, Roshan Mangal [1 ]
Pandiyarajan, Sudhakaran Moopri Singer [1 ]
Saud, Shirjana [1 ]
Kim, Sang Jae [2 ]
Mok, Young Sun [1 ]
机构
[1] Jeju Natl Univ, Dept Chem & Biol Engn, Jeju 63243, South Korea
[2] Jeju Natl Univ, Nanomat & Syst Lab, Dept Mechatron Engn, Jeju 63243, South Korea
基金
新加坡国家研究基金会;
关键词
COBALT MOLYBDATE; ENERGY-STORAGE; GRAPHENE OXIDE; HIGH-POWER; NI FOAM; CARBON; ARRAYS; BATTERY; GLUCOSE; FABRICATION;
D O I
10.1039/d0dt02204g
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
An essential key to enhancing the specific capacity and cyclic stability of transition metal oxide materials is the hybridization of carbon compounds by binder-free methods for supercapacitors. Carbonaceous compounds shorten the electron-ion diffusion pathways due to their high active surface area and conductivity. Herein, we focus on improving the specific energy, stability, and conductivity of the electrode by the incorporation of nanosized carbon material. The integration of nano carbons from viable eco-friendly glucose with CoMoO4 enhanced the experimental specific capacity of the electrode. The self-grown CoMoO4 on a nickel foam (CMO-NF) was confirmed as the best approach after extensive optimization process by the feasible hydrothermal (HT) method. The amount of carbon deposited and the structural morphology on the fabricated CoMoO4-glucose-derived carbon (CMO-GC) electrode was varied by adjusting the concentration of glucose by the viable HT technique. Notably, the hybrid CMO-GC-2 achieved a maximum specific capacity of 851.85 C g(-1) at 1 A g(-1), and it is relatively higher than that of CMO-NF (301.4 C g(-1)). The asymmetric supercapacitor device (CMO-GC-2//AC) demonstrated excellent energy density (36.86 W h kg(-1) for 152.84 W kg(-1)), power density (3209.35 W kg(-1) for 11.19 W h kg(-1)), and extensive capacity retention of 87% for up to 5000 cycles. The high performance is related to the synergetic effect of EDLC and the redox reaction, with nano-architecture and well-defined morphology of the electrode material.
引用
收藏
页码:14506 / 14519
页数:14
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