Hydrogen Storage in High Surface Area Carbons: Experimental Demonstration of the Effects of Nitrogen Doping

被引:174
作者
Xia, Yongde [2 ]
Walker, Gavin S. [2 ]
Grant, David M. [2 ]
Mokaya, Robert [1 ]
机构
[1] Univ Nottingham, Sch Chem, Nottingham NG7 2RD, England
[2] Univ Nottingham, Fac Engn, Div Fuels & Power Technol, Nottingham NG7 2RD, England
基金
英国工程与自然科学研究理事会;
关键词
ORDERED POROUS CARBON; ZEOLITE-TEMPLATED CARBON; CARBIDE-DERIVED CARBONS; MICROPOROUS CARBON; PORE-SIZE; ACTIVATED CARBONS; H-2; STORAGE; ADSORPTION; NANOTUBES; PHYSISORPTION;
D O I
10.1021/ja9054838
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The influence of nitrogen doping on the hydrogen uptake and storage capacity of high surface area carbon materials is presented in this report. To generate suitable study materials, we have exploited the relationship between synthesis conditions and textural properties of zeolite-templated carbons to generate a range of high surface area carbons with similar pore size distribution but which are either N-doped or N-free. For N-doped carbons, the nitrogen content was kept within a narrow range of between 4.7 and 7.7 wt %. The carbon materials, irrespective of whether they were doped or not, exhibited high surface area (1900-3700 m(2)/g) and pore volume (0.99 and 1.88 cm(3)/g), a micropore surface area of 1500-2800 m(2)/g, and a micropore volume of 0.65-1.24 cm(3)/g. The hydrogen uptake varied between 4.1 and 6.9 wt %. We present experimental data that indicates that the effect of N-doping on hydrogen uptake is only apparent when related to the surface area and pore volume associated with micropores rather than total porosity. Furthermore, by considering the isosteric heat of hydrogen adsorption and excess hydrogen uptake on N-free or N-doped carbons, it is shown that N-doping can be beneficial at lower coverage (low hydrogen uptake) but is detrimental at higher coverage (higher hydrogen uptake). The findings are consistent with previous theoretical predictions on the effect of N-doping of carbon on hydrogen uptake. The findings, therefore, add new insights that are useful for the development of carbon materials with enhanced hydrogen storage capacity.
引用
收藏
页码:16493 / 16499
页数:7
相关论文
共 61 条
[1]   The preparation of active carbons from coal by chemical and physical activation [J].
Ahmadpour, A ;
Do, DD .
CARBON, 1996, 34 (04) :471-479
[2]   Role of microporosity in hydrogen adsorption on templated nanoporous carbons [J].
Armandi, M. ;
Bonelli, B. ;
Arean, C. Otero ;
Garrone, E. .
MICROPOROUS AND MESOPOROUS MATERIALS, 2008, 112 (1-3) :411-418
[3]   Nanostructured, nitrogen-doped carbon materials for hydrogen storage [J].
Badzian, A ;
Badzian, T ;
Breval, E ;
Piotrowski, A .
THIN SOLID FILMS, 2001, 398 :170-174
[4]   Storage of hydrogen by physisorption on carbon and nanostructured materials [J].
Benard, Pierre ;
Chahine, Richard .
SCRIPTA MATERIALIA, 2007, 56 (10) :803-808
[5]   Optimum conditions for adsorptive storage [J].
Bhatia, SK ;
Myers, AL .
LANGMUIR, 2006, 22 (04) :1688-1700
[6]   Hydrogen storage capacities of nanoporous carbon calculated by density functional and Moller-Plesset methods [J].
Cabria, I. ;
Lopez, M. J. ;
Alonso, J. A. .
PHYSICAL REVIEW B, 2008, 78 (07)
[7]   The optimum average nanopore size for hydrogen storage in carbon nanoporous materials [J].
Cabria, Ivan ;
Lopez, Maria J. ;
Alonso, Julio A. .
CARBON, 2007, 45 (13) :2649-2658
[8]   Origin of the large N is binding energy in X-ray photoelectron spectra of calcined carbonaceous materials [J].
Casanovas, J ;
Ricart, JM ;
Rubio, J ;
Illas, F ;
JimenezMateos, JM .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1996, 118 (34) :8071-8076
[9]   Hydrogen storage in activated carbons and activated carbon fibers [J].
de la Casa-Lillo, MA ;
Lamari-Darkrim, F ;
Cazorla-Amorós, D ;
Linares-Solano, A .
JOURNAL OF PHYSICAL CHEMISTRY B, 2002, 106 (42) :10930-10934
[10]   Ordered porous carbon with tailored pore size for electrochemical hydrogen storage application [J].
Fang, BZ ;
Zhou, HS ;
Honma, I .
JOURNAL OF PHYSICAL CHEMISTRY B, 2006, 110 (10) :4875-4880