Transition-Metal Oxides Anchored on Nitrogen-Enriched Carbon Ribbons for High-Performance Pseudocapacitors

被引:22
作者
Pang, Yuanchao [1 ]
Zhang, Shuyang [1 ]
Chen, Sheng [1 ]
Liang, Jin [1 ]
Li, Mingyan [1 ]
Ding, Dawei [1 ]
Ding, Shujiang [1 ]
机构
[1] Xi An Jiao Tong Univ, Dept Dept Appl Chem,Sch Sci,Xian Key Lab Sustaina, MOE Key Lab Nonequilibrium Synth & Modulat Conden, State Key Lab Nonequilibrium Synth & Modulat Cond, Xian 710049, Shaanxi, Peoples R China
基金
中国国家自然科学基金;
关键词
biomass; micron-sized carbon ribbons; NiCo2O4; nanosheets; nitrogen doping; supercapacitors; SOLID-STATE SUPERCAPACITOR; REDUCED GRAPHENE OXIDE; ASYMMETRIC SUPERCAPACITORS; ALLYLIC REARRANGEMENT; ELECTRODE MATERIALS; CORE/SHELL ARRAYS; FACILE SYNTHESIS; NANOWIRE ARRAYS; NICKEL FOAM; THIN-FILMS;
D O I
10.1002/chem.201802951
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Increasing demand for effective energy-storage systems derived from low-cost and ecofriendly raw materials has aroused wide concern. In this contribution, we propose nitrogen-abundant amorphous micron-sized carbon ribbons (AMCRs) originating from biomass raupo as a novel substrate due to their specific quasi 2D morphologies and outstanding dispersion ability. Owing to the innate nitrogen atoms on the surface of AMCRs, ultrathin binary and ternary metal oxide (NiO, CoO, and NiCo2O4) nanosheets can be uniformly developed under benign conditions. These three composites were separately fabricated as electrodes for supercapacitors in a three-electrode system and exhibited favorable activities. Among them, the ternary metal oxide composites NiCo2O4@AMCRs delivered the supreme specific capacitance of 1691 Fg(-1) and best cycling stability (89% capacity retention over 10,000 cycles). Moreover, symmetric supercapacitors (NiCo2O4@AMCRs//NiCo2O4@AMCRs) were assembled inside sleeve devices with 2 M KOH aqueous electrolyte, which demonstrated admirable cyclic stability (79.1 % capacity retention over 8,000 cycles), and an excellent energy density of 26 Wh kg(-1) at the power density of 1.8 kW kg(-1).
引用
收藏
页码:16104 / 16112
页数:9
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