Templated synthesis of carbon materials from zeolites (Y, beta, and ZSM-5) and a montmorillonite clay (K10): Physical and electrochemical characterization

被引:125
作者
Meyers, CJ
Shah, SD
Patel, SC
Sneeringer, RM
Bessel, CA
Dollahon, NR
Leising, RA
Takeuchi, ES
机构
[1] Villanova Univ, Dept Chem, Villanova, PA 19085 USA
[2] Villanova Univ, Dept Biol, Villanova, PA 19085 USA
[3] Wilson Greatbatch Ltd, Clarence, NY 14031 USA
来源
JOURNAL OF PHYSICAL CHEMISTRY B | 2001年 / 105卷 / 11期
关键词
D O I
10.1021/jp0029663
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
New high surface area carbon materials were prepared at low temperature (600 degreesC) using zeolite (Y, Beta, and ZSM-5) and montmorillonite clay (K10)templates. Acrylonitrile, furfuryl alcohol, pyrene, and vinyl acetate precursors were polymerized and carbonized in each of the inorganic matrixes without the addition of a polymerizing agent. The templates were removed by acid demineralization and the resulting carbon materials were physically characterized by infrared spectroscopy,BET (N-2) surface area analysis, energy dispersive spectroscopy (EDS), scanning electron microscopy (SEM), and elemental analyses. Electrochemical characterizations were also conducted. Cyclic voltammetry was employed to examine the synthesized carbons in the oxidation of catechol to hydroquinone and quinone, a model reaction that is known to be surface dependent. The identities of both the template and the substrate affected the electrochemical response. Additionally, the ability of the new carbons to intercalate and deintercalate lithium was investigated. While all of the synthesized carbons displayed high irreversible capacities consistent with other low-temperature carbons, the carbons prepared from zeolite Y displayed unique voltage curves, suggesting template effects on the carbon. In addition, all of the carbons prepared for this study displayed significant voltage hysteresis on charge/discharge.
引用
收藏
页码:2143 / 2152
页数:10
相关论文
共 95 条
[1]  
AIHARA M, 1987, ANAL LETT, V20, P669
[2]   CARBON NANOTUBES AS REMOVABLE TEMPLATES FOR METAL-OXIDE NANOCOMPOSITES AND NANOSTRUCTURES [J].
AJAYAN, PM ;
STEPHAN, O ;
REDLICH, P ;
COLLIEX, C .
NATURE, 1995, 375 (6532) :564-567
[3]   TEMPLATE MINERALIZATION OF SELF-ASSEMBLED ANISOTROPIC LIPID MICROSTRUCTURES [J].
ARCHIBALD, DD ;
MANN, S .
NATURE, 1993, 364 (6436) :430-433
[4]   Periodic mesoporous organosilicas with organic groups inside the channel walls [J].
Asefa, T ;
MacLachlan, MJ ;
Coombs, N ;
Ozin, GA .
NATURE, 1999, 402 (6764) :867-871
[5]   TEMPLATING OF MESOPOROUS MOLECULAR-SIEVES BY NONIONIC POLYETHYLENE OXIDE SURFACTANTS [J].
BAGSHAW, SA ;
PROUZET, E ;
PINNAVAIA, TJ .
SCIENCE, 1995, 269 (5228) :1242-1244
[6]   STUDY OF CARBON-SMECTITE COMPOSITES AND CARBONS OBTAINED BY IN-SITU CARBONIZATION OF POLYFURFURYL ALCOHOL [J].
BANDOSZ, TJ ;
PUTYERA, K ;
JAGIELLO, J ;
SCHWARZ, JA .
CARBON, 1994, 32 (04) :659-664
[7]   Pore structure of carbon-mineral nanocomposites and derived carbons obtained by template carbonization [J].
Bandosz, TJ ;
Jagiello, J ;
Putyera, K ;
Schwarz, JA .
CHEMISTRY OF MATERIALS, 1996, 8 (08) :2023-2029
[8]  
Bard A.J., 1980, ELECTROCHEMICAL METH, P290
[9]   A NEW FAMILY OF MESOPOROUS MOLECULAR-SIEVES PREPARED WITH LIQUID-CRYSTAL TEMPLATES [J].
BECK, JS ;
VARTULI, JC ;
ROTH, WJ ;
LEONOWICZ, ME ;
KRESGE, CT ;
SCHMITT, KD ;
CHU, CTW ;
OLSON, DH ;
SHEPPARD, EW ;
MCCULLEN, SB ;
HIGGINS, JB ;
SCHLENKER, JL .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1992, 114 (27) :10834-10843
[10]   ENCAPSULATION OF POLYPYRROLE CHAINS IN ZEOLITE CHANNELS [J].
BEIN, T ;
ENZEL, P .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION IN ENGLISH, 1989, 28 (12) :1692-1694