Overcoming the barrier to graphitization in a polymer-derived nanoporous carbon

被引:61
作者
Burket, Christopher L. [1 ]
Rajagopalan, Ramakrishnan [2 ]
Foley, Henry C. [1 ,2 ,3 ]
机构
[1] Penn State Univ, Dept Chem Engn, University Pk, PA 16802 USA
[2] Penn State Univ, Mat Res Inst, University Pk, PA 16802 USA
[3] Penn State Univ, Dept Chem, University Pk, PA 16802 USA
基金
美国国家科学基金会;
关键词
D O I
10.1016/j.carbon.2007.12.016
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
A new pathway to synthesize a carbon with both nanoporosity and pre-graphitic structures has been discovered by annealing at 2000 degrees C a CO2 activated, non-graphitizing, nanoporous carbon originally derived from polyfurfuryl alcohol. The activation process with CO2 overcomes the barrier to graphitization normally present in this carbon even when treated at high temperature. Gas adsorption analysis, skeletal density measurements, X-ray diffraction, and transmission electron microscopy are utilized to probe the structure of both the non-activated and the activated carbons at 800, 1200, 1800, and 2000 degrees C. The influence of activation time is also examined. Prior to activation the nanopore walls are comprised of several layers of disordered graphenes. Activation eliminates the barrier to graphitization by reducing the number of layers below the limit of detection and by removing carbon material highly susceptible to oxidation. Annealing at 2000 degrees C of the carbon activated to 84% burnoff induces the formation of pre-graphitic domains amongst the nanoporous carbon. The (002) bands corresponding to 20 = 24.3 degrees, 26 degrees, and 26.5 degrees are identified and assigned to amorphous, turbostratic, and graphitic morphologies. A pore volume of 0.50 cm(3) g(-1) localized in pores below 2 nm in size is preserved after annealing. (c) 2007 Elsevier Ltd. All rights reserved.
引用
收藏
页码:501 / 510
页数:10
相关论文
共 27 条
[1]   Simulation of nanoporous carbons: a chemically constrained structure [J].
Acharya, M ;
Strano, MS ;
Mathews, JP ;
Billinge, JL ;
Petkov, V ;
Subramoney, S ;
Foley, HC .
PHILOSOPHICAL MAGAZINE B-PHYSICS OF CONDENSED MATTER STATISTICAL MECHANICS ELECTRONIC OPTICAL AND MAGNETIC PROPERTIES, 1999, 79 (10) :1499-1518
[2]   Genesis of porosity in polyfurfuryl alcohol derived nanoporous carbon [J].
Burket, Christopher L. ;
Rajagopalan, Ramakrishnan ;
Marencic, Andrew P. ;
Dronvajjala, Krishna ;
Foley, Henry C. .
CARBON, 2006, 44 (14) :2957-2963
[3]   The ''falling cards model'' for the structure of microporous carbons [J].
Dahn, JR ;
Xing, W ;
Gao, Y .
CARBON, 1997, 35 (06) :825-830
[4]   Microporosity and optical properties of some activated chars [J].
Duber, S ;
Rouzaud, JN ;
Clinard, C ;
Pusz, S .
FUEL PROCESSING TECHNOLOGY, 2002, 77 :221-227
[5]   EFFECT OF CROSSLINKING ON FORMATION OF GLASSLIKE CARBONS FROM THERMOSETTING RESINS [J].
FITZER, E ;
SCHAFER, W .
CARBON, 1970, 8 (03) :353-&
[6]   CARBOGENIC MOLECULAR-SIEVES - SYNTHESIS, PROPERTIES AND APPLICATIONS [J].
FOLEY, HC .
MICROPOROUS MATERIALS, 1995, 4 (06) :407-433
[7]   CRYSTALLITE GROWTH IN GRAPHITIZING AND NON-GRAPHITIZING CARBONS [J].
FRANKLIN, RE .
PROCEEDINGS OF THE ROYAL SOCIETY OF LONDON SERIES A-MATHEMATICAL AND PHYSICAL SCIENCES, 1951, 209 (1097) :196-&
[8]  
FRANKLIN RE, 1956, NATURE, V177, P239
[9]   Fullerene-related structure of commercial glassy carbons [J].
Harris, PJF .
PHILOSOPHICAL MAGAZINE, 2004, 84 (29) :3159-3167
[10]   High-resolution electron microscopy studies of non-graphitizing carbons [J].
Harris, PJF ;
Tsang, SC .
PHILOSOPHICAL MAGAZINE A-PHYSICS OF CONDENSED MATTER STRUCTURE DEFECTS AND MECHANICAL PROPERTIES, 1997, 76 (03) :667-677