Simultaneous Nitrogen Doping and Reduction of Graphene Oxide

被引:1619
作者
Li, Xiaolin [1 ]
Wang, Hailiang [1 ]
Robinson, Joshua T. [1 ]
Sanchez, Hernan [1 ]
Diankov, Georgi [1 ]
Dai, Hongjie [1 ]
机构
[1] Stanford Univ, Dept Chem, Stanford, CA 94305 USA
关键词
GRAPHITE OXIDE; SHEETS; CARBON; SERIES; XPS;
D O I
10.1021/ja907098f
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
We developed a simple chemical method to obtain bulk quantities of N-doped, reduced graphene oxide (GO) sheets through thermal annealing of GO in ammonia. X-ray photoelectron spectroscopy (XPS) study of GO sheets annealed at various reaction temperatures reveals that N-doping occurs at a temperature as low as 300 degrees C, while the highest doping level of similar to 5% N is achieved at 500 degrees C. N-doping is accompanied by the reduction of GO with decreases in oxygen levels from similar to 28% in as-made GO down to similar to 2% in 1100 degrees C NH3 reacted GO. XPS analysis of the N binding configurations of doped GO finds pyridinic N in the doped samples, with increased quaternary N (N that replaced the carbon atoms in the graphene plane) in GO annealed at higher temperatures (>= 900 degrees C). Oxygen groups in GO were found responsible for reactions with NH3 and C-N bond formation. Prereduced GO with fewer oxygen groups by thermal annealing in H-2 exhibits greatly reduced reactivity with NH3 and a lower N-doping level. Electrical measurements of individual GO sheet devices demonstrate that GO annealed in NH3 exhibits higher conductivity than those annealed in H-2, suggesting more effective reduction of GO by annealing in NH3 than in H-2, consistent with XPS data. The N-doped reduced GO shows clearly n-type electron doping behavior with the Dirac point (DP) at negative gate voltages in three terminal devices. Our method could lead to the synthesis of bulk amounts of N-doped, reduced GO sheets useful for various practical applications.
引用
收藏
页码:15939 / 15944
页数:6
相关论文
共 25 条
[1]   Edge-functionalized and substitutionally doped graphene nanoribbons:: Electronic and spin properties [J].
Cervantes-Sodi, F. ;
Csanyi, G. ;
Piscanec, S. ;
Ferrari, A. C. .
PHYSICAL REVIEW B, 2008, 77 (16)
[2]  
Gao W, 2009, NAT CHEM, V1, P403, DOI [10.1038/nchem.281, 10.1038/NCHEM.281]
[3]   The rise of graphene [J].
Geim, A. K. ;
Novoselov, K. S. .
NATURE MATERIALS, 2007, 6 (03) :183-191
[4]   Altering low-bias transport in zigzag-edge graphene nanostrips with edge chemistry [J].
Gunlycke, D. ;
Li, J. ;
Mintmire, J. W. ;
White, C. T. .
APPLIED PHYSICS LETTERS, 2007, 91 (11)
[5]   A new structural model for graphite oxide [J].
He, HY ;
Klinowski, J ;
Forster, M ;
Lerf, A .
CHEMICAL PHYSICS LETTERS, 1998, 287 (1-2) :53-56
[6]   STUDY OF OXYGEN-CONTAINING GROUPS IN A SERIES OF GRAPHITE OXIDES - PHYSICAL AND CHEMICAL CHARACTERIZATION [J].
HONTORIALUCAS, C ;
LOPEZPEINADO, AJ ;
LOPEZGONZALEZ, JDD ;
ROJASCERVANTES, ML ;
MARTINARANDA, RM .
CARBON, 1995, 33 (11) :1585-1592
[7]   Electrochemical performance of nitrogen-enriched carbons in aqueous and non-aqueous supercapacitors [J].
Hulicova, D ;
Kodama, M ;
Hatori, H .
CHEMISTRY OF MATERIALS, 2006, 18 (09) :2318-2326
[8]   PREPARATION OF GRAPHITIC OXIDE [J].
HUMMERS, WS ;
OFFEMAN, RE .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1958, 80 (06) :1339-1339
[9]   XPS and 15N NMR study of nitrogen forms in carbonaceous solids [J].
Kelemen, SR ;
Afeworki, M ;
Gorbaty, ML ;
Kwiatek, PJ ;
Solum, MS ;
Hu, JZ ;
Pugmire, RJ .
ENERGY & FUELS, 2002, 16 (06) :1507-1515
[10]  
Kinoshita K., 1988, CARBON ELECTROCHEMIC