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Head, Ashley R. (ORCID:0000000187330165)

Publications and source records attributed to Head, Ashley R. (ORCID:0000000187330165).

Cryogenic Reduction of Surface-Bound HKUST-1Crystallites

HKUST-1 is a canonical Cu-based metal-organic framework (MOF) with potential roles in catalysis. A convenient hydroxy double salt templating synthesis was used to produce a thin layer of HKUST-1 crystallites amenable to surface science spec-troscopies under controlled conditions. To study the nature of the Cu sites, N2 and CO2 were adsorbed at cryogenic tempera-tures as passive probe molecules for Cu2+ sites. CO, which is commonly used as a probe molecule of both Cu2+ and Cu1+ sites in porous materials, was found to be a non-innocent probe molecule that reduces the Cu2+ and forms CO2. Isotopically labeled 13CO confirmed the Cu2+ reduction and CO oxidation. The results offer a way to tune Cu oxidation states in HKUST-1, even in the cryogenic temperature regime.

37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗

Tracking the dynamics of catalytic Pt/CeO2 active sites during water-gas-shift reaction

Abstract Understanding the atomistic structure of the active site during catalytic reactions is of paramount importance in both fundamental studies and practical applications, but such studies are challenging due to the complexity of heterogeneous systems. Here, we use Pt/CeO 2 as an example to study the dynamic nature of active sites during the water-gas-shift reaction (WGSR) by combining multiple in situ characterization tools. We show that the different concentrations of interfacial Pt δ+ – O – Ce 4+ moieties at Pt/CeO 2 interfaces are responsible for the rank of catalytic performance of Pt/CeO 2 catalysts: Pt/CeO 2 -rod > Pt/CeO 2 -cube > Pt/CeO 2 -oct. For all the catalysts, metallic Pt is formed during the WGSR, leading to the transformation of the active sites to Pt 0 – O v – Ce 3+ and interface reconstruction. These findings shed light on the nature of the active site for the WGSR on Pt/CeO 2 and highlight the importance of combining complementary in situ techniques for establishing structure-performance relationships.

36 MATERIALS SCIENCE↗