Electrosynthesis of macroporous polyaniline-V2O5 nanocomposites and their unusual magnetic properties

被引:62
作者
Karatchevtseva, Inna [1 ]
Zhang, Zhaoming [1 ]
Hanna, John [1 ]
Luca, Vittorio [1 ]
机构
[1] Australian Nucl Sci & Technol Org, Inst Mat & Engn Sci, Menai, NSW 2234, Australia
关键词
RECHARGEABLE LITHIUM BATTERIES; VANADIA GEL SYNTHESIS; ELECTROCHEMICAL POLYMERIZATION; PEROXOVANADATE PRECURSORS; CONDUCTING POLYANILINE; 3-DIMENSIONAL ARRAYS; V2O5; ANILINE; OXIDE; SPECTROSCOPY;
D O I
10.1021/cm052821e
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
This paper reports a novel two-step one-pot all-electrochemical method for the preparation of interpenetrating conducting-polymer (polyaniline, PANI) semiconducting oxide (V2O5) nanocomposites. In the method, a spongy interconnected PANI network is first deposited on a titanium metal substrate. The electrodeposited PANI network has pores on the order of a few micrometers and is used as a template for the V2O5 component which is also deposited electrochemically. The dimensionality of the amorphous V2O5 that forms can be controlled through control of the current density during the deposition, and this in turn reduces the porosity. As the current density increases and more V2O5 is deposited, Raman and X-ray photoelectron spectroscopy (XPS) indicate that the conductivity of the PANI decreases. Regardless of the current density used in the range 1-5 mA/cm(2), the V-51 solid-state NMR spectrum of the V2O5 component shows a major resonance at about -8500 ppm which is ascribed to a Knight shift due to interaction of the PANI conduction electrons with the V-51 nuclear spin. The magnitude of this V-51 Knight shift is unprecedented exceeding by a significant margin any of those previously reported for vanadium oxide compounds.
引用
收藏
页码:4908 / 4916
页数:9
相关论文
共 63 条
[1]   INITIATING AGENTS FOR ELECTROCHEMICAL POLYMERIZATION OF ANILINE ON TITANIUM ELECTRODES [J].
ABALYAEVA, VV ;
KOGAN, IL .
SYNTHETIC METALS, 1994, 63 (02) :109-113
[2]   Electrochemical study of polyaniline deposited on a titanium surface [J].
Arsov, LD .
JOURNAL OF SOLID STATE ELECTROCHEMISTRY, 1998, 2 (04) :266-272
[3]   Oxidative polymerization of aniline and pyrrole by isopolymetallates of vanadium [J].
Ballav, N ;
Biswas, M .
JOURNAL OF APPLIED POLYMER SCIENCE, 2005, 96 (04) :1483-1486
[4]   Electrochemical syntheses of highly ordered macroporous conducting polymers grown around self-assembled colloidal templates [J].
Bartlett, PN ;
Birkin, PR ;
Ghanem, MA ;
Toh, CS .
JOURNAL OF MATERIALS CHEMISTRY, 2001, 11 (03) :849-853
[5]   ENCAPSULATION OF POLYPYRROLE CHAINS IN ZEOLITE CHANNELS [J].
BEIN, T ;
ENZEL, P .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION IN ENGLISH, 1989, 28 (12) :1692-1694
[6]   SPATIALLY LOCALIZED ELECTRONIC-STRUCTURE IN POLYANILINE BY SCANNING TUNNELING SPECTROSCOPY [J].
BONNELL, DA ;
ANGELOPOULOS, M .
SYNTHETIC METALS, 1989, 33 (03) :301-310
[7]   SPECTROSCOPIC STUDIES OF POLYANILINE IN SOLUTION AND IN SPIN-CAST FILMS [J].
CAO, Y ;
SMITH, P ;
HEEGER, AJ .
SYNTHETIC METALS, 1989, 32 (03) :263-281
[8]   Macroporous vanadium phosphorus oxide phases displaying three-dimensional arrays of spherical voids [J].
Carreon, MA ;
Guliants, VV .
CHEMISTRY OF MATERIALS, 2002, 14 (06) :2670-2675
[9]   Adsorbed surfactants as templates for the synthesis of morphologically controlled polyaniline and polypyrrole nanostructures on flat surfaces: From spheres to wires to flat films [J].
Carswell, ADW ;
O'Rear, EA ;
Grady, BP .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2003, 125 (48) :14793-14800
[10]   POLYANILINE - PROTONIC ACID DOPING OF THE EMERALDINE FORM TO THE METALLIC REGIME [J].
CHIANG, JC ;
MACDIARMID, AG .
SYNTHETIC METALS, 1986, 13 (1-3) :193-205