Intercalation of conductive polyaniline in the mesostructured V2O5

被引:61
作者
Li, ZF [1 ]
Ruckenstein, E [1 ]
机构
[1] SUNY Buffalo, Dept Chem Engn, Buffalo, NY 14260 USA
关键词
D O I
10.1021/la0203887
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Starting from mesoporous V2O5 containing a small amount of Mg, V2O5/PANI (polyaniline) nanocomposites with lamellar and wormlike structures and fibrous morphologies were synthesized. Mesoporous V2O5/Mg was first prepared at room temperature using a binary mixture of surfactants (cetyltrimethylammonium bromide (CTAB) and hexadecylamine (HDA)) as a template and MgCl2 as an ordered structure stabilizer. After a heat treatment and solvent extraction which eliminated the surfactants, the as-synthesized mesostructured V2O5 was subjected to an in situ oxidative intercalation of aniline as polyaniline in the presence of air (V2O5 being the oxidation agent). The V2O5/PANI composite thus obtained kept an ordered mesostructure. The mesostructured V2O5 and V2O5/PANI nanocomposites were characterized by XRD, TEM, and BET/N-2 adsorption analysis. The FTIR of the mesostructured V2O5 and V2O5/PANI nanocomposites has demonstrated that PANI chains were intercalated into the mesostructured V2O5/Mg. The electrical conductivity of PANI/V2O5 nanocomposite reached values of the order of 10(-2) S/cm, which is by 5 orders of magnitude higher than that of the mesostructured V2O5/Mg. It was found that the aging in air facilitated the chain growth of PANI in the mesopores, thus increasing the electrical conductivity. It should be emphasized that the aging time needed to reach a relatively high conductivity of the mesostructured V2O5/PANI composites was shorter than those of the V2O5 xerogels/PANI. This occurred because the former possesses larger pores than the latter, and this facilitated the growth of the PANI chains.
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页码:6956 / 6961
页数:6
相关论文
共 38 条
[1]   Mesoporous aluminoborates [J].
Ayyappan, S ;
Rao, CNR .
CHEMICAL COMMUNICATIONS, 1997, (06) :575-576
[2]   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
[3]   Lithium insertion into host materials: the key to success for Li ion batteries [J].
Broussely, M ;
Biensan, P ;
Simon, B .
ELECTROCHIMICA ACTA, 1999, 45 (1-2) :3-22
[4]   Effect of the nature of the templating surfactant on the synthesis and structure of mesoporous V-Mg-O [J].
Chao, ZS ;
Ruckenstein, E .
LANGMUIR, 2002, 18 (03) :734-743
[5]   High surface area zirconia by digestion of zirconium propoxide at different pH [J].
Chuah, GK ;
Liu, SH ;
Jaenicke, S ;
Li, J .
MICROPOROUS AND MESOPOROUS MATERIALS, 2000, 39 (1-2) :381-392
[6]   Electrochemical properties of assembled polypyrrole/V2O5 xerogel films [J].
Demets, GJF ;
Anaissi, FJ ;
Toma, HE .
ELECTROCHIMICA ACTA, 2000, 46 (04) :547-554
[7]  
Gomez-Romero P, 2001, ADV MATER, V13, P163, DOI 10.1002/1521-4095(200102)13:3<163::AID-ADMA163>3.0.CO
[8]  
2-U
[9]   Synthesis of polyaniline-intercalated graphite oxide [J].
Higashika, S ;
Kimura, K ;
Matsuo, Y ;
Sugie, Y .
CARBON, 1999, 37 (02) :354-356
[10]   Chemical and electrochemical characterization of a novel nanocomposite formed from V2O5 and Poly(N-propane sulfonic acid aniline), a self-doped polyaniline [J].
Huguenin, F ;
Gambardella, MTD ;
Torresi, RM ;
de Torresi, SI ;
Buttry, DA .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 2000, 147 (07) :2437-2444