TY - JOUR
T1 - TiO2-supported Pt single atoms by surface organometallic chemistry for photocatalytic hydrogen evolution.
AU - Jeantelot, Gabriel
AU - Qureshi, Muhammad
AU - Harb, Moussab
AU - Ould-Chikh, Samy
AU - Anjum, Dalaver H.
AU - Abou-Hamad, Edy
AU - Aguilar-Tapia, Antonio
AU - Hazemann, Jean-Louis
AU - Takanabe, Kazuhiro
AU - Basset, Jean-Marie
N1 - KAUST Repository Item: Exported on 2020-10-01
Acknowledgements: This 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.
PY - 2019/11/2
Y1 - 2019/11/2
N2 - A 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.
AB - A 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.
UR - http://hdl.handle.net/10754/660086
UR - http://xlink.rsc.org/?DOI=C9CP04470A
UR - http://www.scopus.com/inward/record.url?scp=85075109287&partnerID=8YFLogxK
U2 - 10.1039/c9cp04470a
DO - 10.1039/c9cp04470a
M3 - Article
C2 - 31674630
SN - 1463-9076
VL - 21
SP - 24429
EP - 24440
JO - Physical chemistry chemical physics : PCCP
JF - Physical chemistry chemical physics : PCCP
IS - 44
ER -
