In Situ Loading Transition Metal Oxide Clusters on TiO2 Nanosheets As Co-catalysts for Exceptional High Photoactivity

• Published in: ACS catalysis Vol. 3; no. 9; pp. 2052 - 2061
• Main Authors: Liu, Lichen, Ji, Zeyang, Zou, Weixin, Gu, Xianrui, Deng, Yu, Gao, Fei, Tang, Changjin, Dong, Lin
• Format: Journal Article
• Language: English
• Published: American Chemical Society 06.09.2013
• Subjects: photocatalytic O2 evolution; interfacial charge transfer; heterojunctions; TiO2 nanosheets; metal oxide clusters
• ISSN: 2155-5435; 2155-5435
• DOI: 10.1021/cs4002755

In this work, transition metal oxide clusters (MnO x , FeO x , CoO x , NiO x , and CuO x , denoted as TM-TiO2) are in situ loaded on TiO2 nanosheets through one-pot reaction. Structural and pore structural characterizations prove that metal ions do not dope into the frameworks of TiO2 nanosheets. Through TEM and STEM, we can determine that clusters with ∼2 nm size are finely dispersed on TiO2 nanosheets. PL spectra and photoelectrochemical measurements suggest that these metal oxide clusters can serve as hole traps. Time-resolved PL spectra demonstrate that the charge-transfer process in TM-TiO2 is significantly accelerated, leading to higher charge separation efficiency. Metal oxide clusters show significant promotion effect in photocatalytic water oxidation to O2 compared to RuO2/TiO2 and IrO2/TiO2 nanosheets (denoted as Ru-TiO2(IM) and Ir-TiO2(IM)) prepared through conventional impregnation method. We also prepared RuO2/TiO2 and Ir/TiO2 nanosheets (denoted as Ru-TiO2(HT) and Ir-TiO2(HT)) through the in situ loading method. Ru-TiO2(HT) and Ir-TiO2(HT) show O2 evolution rates much better than those of Ru-TiO2(IM) and Ir-TiO2(IM) due to the smaller sizes of RuO2 and IrO2. However, Mn-TiO2 and Co-TiO2 still display better photoactivities compared to those of Ru-TiO2(HT) and Ir-TiO2(HT). These results indicate that transition metal oxides with small sizes can also work as co-catalysts in photocatalysis to substitute noble metal oxides.