Co@Carbon and Co3O4@Carbon nanocomposites derived from a single MOF for supercapacitors

被引:104
作者
Dai, Engao [1 ]
Xu, Jiao [1 ]
Qiu, Junjie [1 ]
Liu, Shucheng [1 ]
Chen, Ping [1 ]
Liu, Yi [1 ]
机构
[1] Guizhou Univ, Sch Phys Sci, Guiyang 550025, Guizhou, Peoples R China
基金
中国国家自然科学基金;
关键词
METAL-ORGANIC FRAMEWORK; DOPED POROUS CARBON; RAMAN-SPECTROSCOPY; NANOPOROUS CARBON; GRAPHENE; NANOSHEETS; COBALT; COMPOSITES; ELECTRODES; REDUCTION;
D O I
10.1038/s41598-017-12733-5
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Developing a composite electrode containing both carbon and transition metal/metal oxide as the supercapacitor electrode can combine the merits and mitigate the shortcomings of both the components. Herein, we report a simple strategy to prepare the hybrid nanostructure of Co@Carbon and Co3O4@Carbon by pyrolysis a single MOFs precursor. Co-based MOFs (Co-BDC) nanosheets with morphology of regular parallelogram slice have been prepared by a bottom-up synthesis strategy. One-step pyrolysis of Co-BDC, produces a porous carbon layer incorporating well-dispersed Co and Co3O4 nanoparticles. The as-prepared cobalt-carbon composites exhibit the thin layer morphology and large specific surface area with hierarchical porosity. These features significantly improve the ion-accessible surface area for charge storage and shorten the ion transport length in thin dimension, thus contributing to a high specific capacitance. Improved capacitance performance was successfully realized for the asymmetric supercapacitors (ASCs) (Co@Carbon//Co3O4@Carbon), better than those of the symmetric supercapacitors (SSCs) based on Co@Carbon and Co3O4@Carbon materials (i.e., Co@Carbon//Co@ Carbon and Co3O4@Carbon//Co3O4@Carbon). The working voltage of the ASCs can be extended to 1.5 V and show a remarkable high power capability in aqueous electrolyte. This work provides a controllable strategy for nanostructured carbon-metal and carbon-metal oxide composite electrodes from a single precursor.
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页数:11
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