TY - JOUR
T1 - Green synthesis of biphasic TiO 2-reduced graphene oxide nanocomposites with highly enhanced photocatalytic activity
AU - Sher Shah, Md Selim Arif
AU - Park, A. Reum
AU - Zhang, Kan
AU - Park, Jong Hyeok
AU - Yoo, Pil J.
PY - 2012/8/22
Y1 - 2012/8/22
N2 - A series of TiO 2-reduced graphene oxide (RGO) nanocomposites were prepared by simple one-step hydrothermal reactions using the titania precursor, TiCl 4 and graphene oxide (GO) without reducing agents. Hydrolysis of TiCl 4 and mild reduction of GO were simultaneously carried out under hydrothermal conditions. While conventional approaches mostly utilize multistep chemical methods wherein strong reducing agents, such as hydrazine, hydroquinone, and sodium borohydride are employed, our method provides the notable advantages of a single step reaction without employing toxic solvents or reducing agents, thereby providing a novel green synthetic route to produce the nanocomposites of RGO and TiO 2. The as-synthesized nanocomposites were characterized by several crystallographic, microscopic, and spectroscopic characterization methods, which enabled confrimation of the robustness of the suggested reaction scheme. Notably, X-ray diffraction and transmission electron micrograph proved that TiO 2 contained both anatase and rutile phases. In addition, the photocatalytic activities of the synthesized composites were measured for the degradation of rhodamine B dye. The catalyst also can degrade a colorless dye such as benzoic acid under visible light. The synthesized nanocomposites of biphasic TiO 2 with RGO showed enhanced catalytic activity compared to conventional TiO 2 photocatalyst, P25. The photocatalytic activity is strongly affected by the concentration of RGO in the nanocomposites, with the best photocatalytic activity observed for the composite of 2.0 wt % RGO. Since the synthesized biphasic TiO 2-RGO nanocomposites have been shown to effectively reduce the electron-hole recombination rate, it is anticipated that they will be utilized as anode materials in lithium ion batteries.
AB - A series of TiO 2-reduced graphene oxide (RGO) nanocomposites were prepared by simple one-step hydrothermal reactions using the titania precursor, TiCl 4 and graphene oxide (GO) without reducing agents. Hydrolysis of TiCl 4 and mild reduction of GO were simultaneously carried out under hydrothermal conditions. While conventional approaches mostly utilize multistep chemical methods wherein strong reducing agents, such as hydrazine, hydroquinone, and sodium borohydride are employed, our method provides the notable advantages of a single step reaction without employing toxic solvents or reducing agents, thereby providing a novel green synthetic route to produce the nanocomposites of RGO and TiO 2. The as-synthesized nanocomposites were characterized by several crystallographic, microscopic, and spectroscopic characterization methods, which enabled confrimation of the robustness of the suggested reaction scheme. Notably, X-ray diffraction and transmission electron micrograph proved that TiO 2 contained both anatase and rutile phases. In addition, the photocatalytic activities of the synthesized composites were measured for the degradation of rhodamine B dye. The catalyst also can degrade a colorless dye such as benzoic acid under visible light. The synthesized nanocomposites of biphasic TiO 2 with RGO showed enhanced catalytic activity compared to conventional TiO 2 photocatalyst, P25. The photocatalytic activity is strongly affected by the concentration of RGO in the nanocomposites, with the best photocatalytic activity observed for the composite of 2.0 wt % RGO. Since the synthesized biphasic TiO 2-RGO nanocomposites have been shown to effectively reduce the electron-hole recombination rate, it is anticipated that they will be utilized as anode materials in lithium ion batteries.
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U2 - 10.1021/am301287m
DO - 10.1021/am301287m
M3 - Article
C2 - 22788800
AN - SCOPUS:84865254000
SN - 1944-8244
VL - 4
SP - 3893
EP - 3901
JO - ACS Applied Materials and Interfaces
JF - ACS Applied Materials and Interfaces
IS - 8
ER -