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Controlling hot electron flux and catalytic selectivity with nanoscale metal-oxide interfaces

Interaction between metal and oxides is an important molecular-level factor that influences the selectivity of a desirable reaction. Therefore, designing a heterogeneous catalyst where metal-oxide interfaces are well-formed is important for understanding selectivity and surface electronic excitation...

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Detalles Bibliográficos
Autores principales: Lee, Si Woo, Kim, Jong Min, Park, Woonghyeon, Lee, Hyosun, Lee, Gyu Rac, Jung, Yousung, Jung, Yeon Sik, Park, Jeong Young
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7782808/
https://www.ncbi.nlm.nih.gov/pubmed/33397946
http://dx.doi.org/10.1038/s41467-020-20293-y
Descripción
Sumario:Interaction between metal and oxides is an important molecular-level factor that influences the selectivity of a desirable reaction. Therefore, designing a heterogeneous catalyst where metal-oxide interfaces are well-formed is important for understanding selectivity and surface electronic excitation at the interface. Here, we utilized a nanoscale catalytic Schottky diode from Pt nanowire arrays on TiO(2) that forms a nanoscale Pt-TiO(2) interface to determine the influence of the metal-oxide interface on catalytic selectivity, thereby affecting hot electron excitation; this demonstrated the real-time detection of hot electron flow generated under an exothermic methanol oxidation reaction. The selectivity to methyl formate and hot electron generation was obtained on nanoscale Pt nanowires/TiO(2), which exhibited ~2 times higher partial oxidation selectivity and ~3 times higher chemicurrent yield compared to a diode based on Pt film. By utilizing various Pt/TiO(2) nanostructures, we found that the ratio of interface to metal sites significantly affects the selectivity, thereby enhancing chemicurrent yield in methanol oxidation. Density function theory (DFT) calculations show that formation of the Pt-TiO(2) interface showed that selectivity to methyl formate formation was much larger in Pt nanowire arrays than in Pt films because of the different reaction mechanism.