TiO2-supported Pt single atoms by surface organometallic chemistry for photocatalytic hydrogen evolution.
Anjum, Dalaver H.
KAUST DepartmentCatalysis for Energy Conversion (CatEC)
Chemical Science Program
Imaging and Characterization Core Lab
KAUST Catalysis Center (KCC)
Kaust Catalysis Center (KCC), Physical Science and Engineering Division (PSE), King Abdullah University of Science and Technology (KAUST), Thuwal 23955-6900, Saudi Arabia.
Physical Science and Engineering (PSE) Division
Embargo End Date2020-11-02
Permanent link to this recordhttp://hdl.handle.net/10754/660086
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AbstractA platinum complex, (CH3)2Pt(COD), is grafted via surface organometallic chemistry (SOMC) on morphology-controlled anatase TiO2 to generate single, isolated Pt atoms on TiO2 nano-platelets. The resulting material is characterized by FT-IR, high resolution scanning transmission electron microscopy (HRSTEM), NMR, and XAS, and then used to perform photocatalytic water splitting. The photocatalyst with SOMC-grafted Pt shows superior performance in photocatalytic hydrogen evolution and strongly suppresses the backwards reaction of H2 and O2 forming H2O under dark conditions, compared to the photocatalyst prepared by impregnation at the same Pt loading. However, single Pt atoms on this surface also rapidly coalesce into nanoparticles under photocatalytic conditions. It is also found that adsorption of CO gas at room temperature also triggers the aggregation of Pt single atoms into nanoparticles. A detailed mechanism is investigated for the mobility of Pt in the formation of its carbonyls using density functional theory (DFT) calculations.
CitationJeantelot, G., Qureshi, M., Harb, M., Ould-Chikh, S., Anjum, D. H., Abou-Hamad, E., … Basset, J.-M. (2019). TiO2-supported Pt single atoms by surface organometallic chemistry for photocatalytic hydrogen evolution. Physical Chemistry Chemical Physics. doi:10.1039/c9cp04470a
SponsorsThis work was supported by the King Abdullah University of Science and Technology (KAUST). We warmly acknowledge the help of KAUST Core labs, and the Supercomputing Laboratory at KAUST for the CPU time attributed to this research work. The FAME-UHD project is financially supported by the French “large loan” EquipEx (EcoX, ANR-10-EQPX-27-01), the CEA-CNRS CRG consortium and the INSU CNRS institute.
PublisherRoyal Society of Chemistry (RSC)