Plasmon-induced catalytic CO hydrogenation by a nano-sheet Pt/HMoO hybrid with abundant surface oxygen vacancies

• Published in: Journal of materials chemistry. A, Materials for energy and sustainability Materials for energy and sustainability, 2021-06, Vol.9 (24), p.13898-1397
• Main Authors: Ge, Hao, Kuwahara, Yasutaka, Kusu, Kazuki, Yamashita, Hiromi
• Format: Article
• ISSN: 2050-7488; 2050-7496
• DOI: 10.1039/d1ta02277f

Taking full advantage of solar light to promote CO 2 hydrogenation remains a challenge in the catalysis field. Combining a degeneratively-doped metal oxide and a precious metal to obtain hybrids with plasmonic absorption in the visible-light region enables the high-efficiency utilization of solar light in photothermal catalysis. Herein, MoO 3 samples with different morphologies were synthesized and combined with Pt to form hybrid materials with a strong plasmonic effect. Among the Pt/MoO 3 hybrids with various morphologies, the Pt/H x MoO 3− y (Sheet) hybrid displayed the best performance in the photothermal synergistic catalysis of the reverse water-gas shift (RWGS) reaction at 140 °C under visible light irradiation because of the advantages of its nanosheet structure ( e.g. , a high specific surface area, high proportion of exposed surface atoms, and good optical transparency). The Pt/H x MoO 3− y (Sheet) catalyst outperformed Pt/H x MoO 3− y hybrids with a bulk, belt, or rod morphology. Thermogravimetry, UV-vis-NIR diffuse reflectance spectroscopy, and model reactions demonstrated that the Pt/H x MoO 3− y (Sheet) hybrid contained the largest amount of surface O vacancies and exhibited the strongest plasmonic absorption, which are the primary reasons for its highest catalytic activity among the investigated hybrid catalysts. Photoelectric characterization revealed that the Pt/H x MoO 3− y (Sheet) hybrid could generate hot electrons under visible-light irradiation. X-ray photoelectron spectroscopy measurements showed a reversible redox event of the Mo atoms, demonstrating that the O vacancies in Pt/H x MoO 3− y (Sheet) acted as active sites and regenerated during the reaction. A possible mechanism is proposed for the photothermal synergistic catalysis in the RWGS reaction. The nanosheet-structured Pt/H x MoO 3− y hybrid can exploit solar energy to greatly reduce energy consumption during the CO 2 hydrogenation reaction, providing a greener and energy-saving scheme for the conversion of CO 2 to CO. The hybrid of nanosheet-structured H x MoO 3− y coupled with Pt exhibits efficient photothermal catalytic hydrogenation of CO 2 .