Chemical Doping of Large-Area Stacked Graphene Films for Use as Transparent, Conducting Electrodes

被引:317
作者
Kasry, Amal [1 ,2 ]
Kuroda, Marcelo A. [1 ,3 ]
Martyna, Glenn J. [1 ]
Tulevski, George S. [1 ]
Bol, Ageeth A. [1 ]
机构
[1] IBM Corp, Thomas J Watson Res Ctr, Yorktown Hts, NY 10598 USA
[2] Egypt Nanotechnol Res Ctr, Giza 12577, Egypt
[3] Univ Illinois, Dept Comp Sci, Urbana, IL 61801 USA
关键词
graphene; doping; transparent conductive electrodes; solar cells; resistor network; stacking; OXIDE-FILMS; PHASE;
D O I
10.1021/nn100508g
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Graphene is considered a leading candidate to replace conventional transparent conducting electrodes because of its high transparency and exceptional transport properties. The effect of chemical p-type doping on graphene stacks was studied in order to reduce the sheet resistance of graphene films to values approaching those of conventional transparent conducting oxides. In this report, we show that large-area, stacked graphene films are effectively p-doped with nitric acid. The doping decreases the sheet resistance by a factor of 3, yielding films comprising eight stacked layers with a sheet resistance of 90 Omega/square at a transmittance of 80%. The films were doped either after all of the layers were stacked (last-layer-doped) or after each layer was added (interlayer-doped). A theoretical model that accurately describes the stacked graphene film system as a resistor network was developed. The model defines a characteristic transfer length where all the channels in the graphene films actively contribute to electrical transport. The experimental data shows a linear increase in conductivity with the number of graphene layers, indicating that each layer provides an additional transport channel, in good agreement with the theoretical model.
引用
收藏
页码:3839 / 3844
页数:6
相关论文
共 34 条
[1]   Reversibility, dopant desorption, and tunneling in the temperature-dependent conductivity of type-separated, conductive carbon nanotube networks [J].
Barnes, Teresa M. ;
Blackburn, Jeffrey L. ;
van de Lagemaat, Jao ;
Coutts, Timothy J. ;
Heben, Michael J. .
ACS NANO, 2008, 2 (09) :1968-1976
[2]   Evaluation of solution-processed reduced graphene oxide films as transparent conductors [J].
Becerril, Hdctor A. ;
Mao, Jie ;
Liu, Zunfeng ;
Stoltenberg, Randall M. ;
Bao, Zhenan ;
Chen, Yongsheng .
ACS NANO, 2008, 2 (03) :463-470
[3]   Graphene-based liquid crystal device [J].
Blake, Peter ;
Brimicombe, Paul D. ;
Nair, Rahul R. ;
Booth, Tim J. ;
Jiang, Da ;
Schedin, Fred ;
Ponomarenko, Leonid A. ;
Morozov, Sergey V. ;
Gleeson, Helen F. ;
Hill, Ernie W. ;
Geim, Andre K. ;
Novoselov, Kostya S. .
NANO LETTERS, 2008, 8 (06) :1704-1708
[4]   A mechanical assessment of flexible optoelectronic devices [J].
Chen, Z ;
Cotterell, B ;
Wang, W ;
Guenther, E ;
Chua, SJ .
THIN SOLID FILMS, 2001, 394 (1-2) :201-205
[5]   ITO/Ag/ITO multilayer films for the application of a very low resistance transparent electrode [J].
Choi, KH ;
Kim, JY ;
Lee, YS ;
Kim, HJ .
THIN SOLID FILMS, 1999, 341 (1-2) :152-155
[6]   Structural coherency of graphene on Ir(111) [J].
Coraux, Johann ;
N'Diaye, Alpha T. ;
Busse, Carsten ;
Michely, Thomas .
NANO LETTERS, 2008, 8 (02) :565-570
[7]   INTERCALATION COMPOUNDS OF GRAPHITE [J].
DRESSELHAUS, MS ;
DRESSELHAUS, G .
ADVANCES IN PHYSICS, 1981, 30 (02) :139-326
[8]   Chemical Doping and Electron-Hole Conduction Asymmetry in Graphene Devices [J].
Farmer, Damon B. ;
Golizadeh-Mojarad, Roksana ;
Perebeinos, Vasili ;
Lin, Yu-Ming ;
Tulevski, George S. ;
Tsang, James C. ;
Avouris, Phaedon .
NANO LETTERS, 2009, 9 (01) :388-392
[9]   Inelastic neutron scattering study of the proton dynamics in HNO3 graphite intercalation compounds [J].
Fillaux, F ;
Menu, S ;
Conard, J ;
Fuzellier, H ;
Parker, SW ;
Hanon, AC ;
Tomkinson, J .
CHEMICAL PHYSICS, 1999, 242 (02) :273-281
[10]   The rise of graphene [J].
Geim, A. K. ;
Novoselov, K. S. .
NATURE MATERIALS, 2007, 6 (03) :183-191