Enhanced Photocatalytic Activity of Chemically Bonded TiO2/Graphene Composites Based on the Effective Interfacial Charge Transfer through the C–Ti Bond

• Published in: ACS catalysis 2013-07, Vol.3 (7), p.1477-1485
• Main Authors: Huang, Qingwu, Tian, Shouqin, Zeng, Dawen, Wang, Xiaoxia, Song, Wulin, Li, Yingying, Xiao, Wei, Xie, Changsheng
• Format: Article
• Language: eng ; jpn
• ISSN: 2155-5435; 2155-5435
• DOI: 10.1021/cs400080w

Recently, graphene-based semiconductor photocatalysts have attracted more attention because of their enhanced photocatalytic activity caused by interfacial charge transfer (IFCT). However, the effect of a chemical bond is rarely involved for the IFCT. In this work, TiO2/graphene composites with a chemically bonded interface were prepared by a facile solvothermal method using tetrabutyl orthotitanate (TBOT) as the Ti source. The chemically bonded TiO2/graphene composites effectively enhanced their photocatalytic activity in photodegradation of formaldehyde in air, and the graphene content exhibited an obvious influence on the photocatalytic activity. The prepared composite with 2.5 wt % graphene (G2.5-TiO2) showed the highest photocatalytic activity, exceeding that of Degussa P25, as-prepared pure TiO2 nanoparticles, and the mechanically mixed TiO2/graphene (2.5 wt %) composite by a factor of 1.5, 2.6, and 2.3, respectively. The enhancement in the photocatalytic activity was attributed to the synergetic effect between graphene and TiO2 nanoparticles. Other than the graphene as an excellent electron acceptor and transporter, the enhanced photocatalytic activity was caused by IFCT through a C–Ti bond, which markedly decreased the recombination of electron–hole pairs and increased the number of holes participating in the photooxidation process, confirmed by XPS analysis, the gaseous phase transient photocurrent response, electrochemical impedance spectroscopy, and photoluminescence spectra. This work about effective IFCT through a chemically bonded interface can provide new insights for directing the design of new heterogeneous photocatalysts, which can be applied in environmental protection, water splitting, and photoelectrochemical conversion.