Single step synthesis of chitin/chitosan-based graphene oxide-ZnO hybrid composites for better electrical conductivity and optical properties

被引:45
作者
Anandhavelu, S. [1 ]
Thambidurai, S. [1 ]
机构
[1] Alagappa Univ, Sch Chem Sci, Dept Ind Chem, Karaikkudi 630003, Tamil Nadu, India
关键词
Chitin; Graphene oxide-ZnO; Hybrid composites; Optical properties; Electrical conductivity; EXFOLIATED GRAPHITE OXIDE; FUNCTIONALIZED GRAPHENE; CHITIN DEACETYLATION; CARBON NANOTUBES; RAMAN-SPECTRA; SOLAR-CELLS; NANOCOMPOSITES; CHITOSAN; NANOPARTICLES; SHEETS;
D O I
10.1016/j.electacta.2012.12.024
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
We synthesized two composites/hybrid composites with a graphene oxide (GO)/mixed GO-ZnO filler using either a chitin or a chitosan matrix. Fourier transform infrared spectroscopy analysis confirmed that chitin had been converted to chitosan during matrix fabrication because only chitosan, ZnO and GO were shown to be present in the composites/hybrid composites. Raman spectroscopy indicated the display of D and G bands at 1345 cm(-1) and 1584 cm(-1), respectively. UV absorption peaks appeared at 260-360 nm and 201 nm in both hybrid composites, which indicate a strong binding of ZnO within the chitosan-GO sheets. High resolution scanning electron microscopy and atomic force microscopy studies demonstrated that on a molecular scale ZnO was well dispersed in the hybrid composites. Impedance spectroscopy and a four-probe resistivity method were used for room temperature electrical conductivity measurements. The electrical conductivity of the chitin-based GO-ZnO hybrid composites was estimated to be similar to 5.94 x 10(6) S/cm and was greater than that of the chitosan-based GO-ZnO hybrid composite (similar to 4.13 x 10(6) S/cm). The chitin-based GO-ZnO hybrid composite had a higher optical band gap (3.4 eV) than the chitosan-based GO-ZnO hybrid composite (3.0 eV). The current-voltage measurement showed that electrical sheets resistance of the chitosan-based composites decreased with formation of ZnO. (C) 2012 Elsevier Ltd. All rights reserved.
引用
收藏
页码:194 / 202
页数:9
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