Nitrogen doped superporous carbon prepared by a mild method. Enhancement of supercapacitor performance

被引:40
作者
Jose Mostazo-Lopez, Maria [1 ,2 ]
Ruiz-Rosas, Ramiro [1 ,2 ]
Morallon, Emilia [2 ,3 ]
Cazorla-Amoros, Diego [1 ,2 ]
机构
[1] Univ Alicante, Dept Quim Inorgan, Apartado 99, E-03080 Alicante, Spain
[2] Univ Alicante, Inst Univ Mat, Apartado 99, E-03080 Alicante, Spain
[3] Univ Alicante, Dept Quim Fis, Apartado 99, E-03080 Alicante, Spain
关键词
Activated carbons; Surface chemistry; Nitrogen doped carbons; Supercapacitors; ACTIVATED CARBONS; FUNCTIONAL-GROUPS; ELECTROCHEMICAL CHARACTERIZATION; SURFACE-CHEMISTRY; CAPACITANCE; ELECTRODES; NANOTUBES; FIBERS;
D O I
10.1016/j.ijhydene.2016.03.091
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
Nitrogen functionalization (ca. 4 at. % N-xps) of a highly microporous activated carbon (S-BET > 3000 m(2)/g) has been achieved by two different approaches at mild conditions: (i) oxidation and post-reaction with nitrogen reactants, and (ii) direct reaction of pristine carbon material with nitrogen reactants. Interestingly, the introduction of nitrogen functionalities allows full preservation of the microporosity when pathway (ii) is followed. The electrochemical performance of the carbon materials as electrodes for supercapacitors was evaluated by using symmetric and asymmetric configuration in 1 M H2SO4. Both nitrogenfunctionalized carbon materials showed larger stability and energy efficiency than the pristine carbon material when working at 1.4 V. The non-oxidized and functionalized activated carbon evidences the best performance as electrode for supercapacitor, providing energy and power density of 14.5 Wh/kg and 61.2 kW/kg and keeping 83% of original capacitance after 5000 charge discharge cycles. This improvement is related to the presence of surface nitrogen functionalities that provide a higher electrochemical stability, avoiding the formation of detrimental oxygen groups during the operation of the supercapacitor. (C) 2016 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:19691 / 19701
页数:11
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