Constructing micropore-rich nitrogen-doped carbon for high-performance supercapacitor and adsorption of carbon dioxide

被引:5
|
作者
Sahu, Priya [1 ,2 ]
Mishra, Ranjit [1 ,2 ]
Panigrahy, Sonali [1 ,2 ]
Panda, Prajnashree [1 ,2 ]
Barman, Sudip [1 ,2 ]
机构
[1] Natl Inst Sci Educ & Res NISER, Sch Chem Sci, Bhubaneswar 752050, Odisha, India
[2] Homi Bhabha Natl Inst, Mumbai, Maharashtra, India
关键词
activation; electrode; heteroatom; micropore; physisorption; HIERARCHICALLY POROUS CARBON; ELECTROCHEMICAL ENERGY-STORAGE; ADVANCED ELECTRODE MATERIALS; ACTIVATED CARBON; CO2; CAPTURE; GRAPHITIC CARBON; AREA; NANOSHEETS;
D O I
10.1002/er.8075
中图分类号
TE [石油、天然气工业]; TK [能源与动力工程];
学科分类号
0807 ; 0820 ;
摘要
Design of advanced highly porous heteroatom-doped carbon is desirable for their wide presence in applications like electrochemical energy storage systems, gas adsorption, and separation processes. In this work, porous nitrogen-doped carbon was developed from ethylenediamine via an in situ self-doping solvothermal process followed by pyrolysis and KOH activation under high temperature. Micropore-rich nitrogen-containing carbon materials were prepared through variation of the KOH/C ratio during activation and their electrochemical performance in alkaline electrolyte as well as CO2 sorption behaviour was evaluated. The porous carbon developed using KOH/C ratio of 2 delivered highest supercapacitor performance in 6 M KOH achieving high specific capacitance of 353 F g(-1) with 1 A g(-1) of current due to its high pore volume and micropore rich surface. The functionalized carbon delivered CO2 uptake capacities of 4.48 and 3.0 mmol g(-1) under temperatures of 273 and 298 K, respectively, at 1 bar pressure with a good CO2/N-2 selectivity of 20.58 and CO2/CH4 selectivity of 3.83. The existence of nitrogen functional groups, high surface area, and micropore-rich porous structures may be the essential reasons behind superior electrode performance and CO2 capture capacity of the material. This work hopefully offers a simple development of N-doped carbon for effective energy storage and CO2 adsorption systems.
引用
收藏
页码:13556 / 13569
页数:14
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