Interplay between the metal- support interaction and stability in Pt/ Co3O4(111) model catalysts

Kód výsledku v IS VaVaI

<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216208%3A11320%2F18%3A10391197" target="_blank" >RIV/00216208:11320/18:10391197 - isvavai.cz</a>

Výsledek na webu

<a href="https://doi.org/10.1039/c8ta08142e" target="_blank" >https://doi.org/10.1039/c8ta08142e</a>

DOI - Digital Object Identifier

<a href="http://dx.doi.org/10.1039/c8ta08142e" target="_blank" >10.1039/c8ta08142e</a>

Jazyk výsledku

angličtina

Název v původním jazyce

Interplay between the metal- support interaction and stability in Pt/ Co3O4(111) model catalysts

Popis výsledku v původním jazyce

The interplay between the metal-support interaction and stability with respect to sintering has been investigated for Pt nanoparticles supported on well-ordered Co3O4(111)/Ir(100) films in UHV and under oxidizing conditions by means of synchrotron radiation photoelectron spectroscopy (SRPES) and near ambient pressure X-ray photoelectron spectroscopy (NAP XPS). The electronic metal-support interaction between Pt and Co3O4(111) associated with charge transfer results in partial reduction of Co3O4(111) yielding partially oxidized Pt+ species at the interface. The stability of the supported Pt particles is coupled with the oxidation state of Pt+ species, which can be reduced or oxidized depending on the Pt coverage and reactive environment. Annealing of Pt/Co3O4(111)/Ir(100) in UHV triggers the reduction of Pt+ species. At higher temperature, reverse spillover of oxygen to the Pt nanoparticles is accompanied by reduction of Co3O4(111). Under these conditions, the oxidation state of Pt+ species depends strongly on Pt coverage. Thus, at low Pt coverage (0.3 ML Pt), Pt+ is converted to Pt4+, at intermediate coverage (1.3 ML Pt), Pt+ remains stable, and at high Pt coverage (1.93 ML), Pt+ is reduced to Pt-0. Sintering of Pt particles is associated with the reduction of the Pt+ species. This process is prevented under oxidizing conditions due to the formation of an interfacial oxide PtOx. The formation of an interfacial PtOx is observed at 300 K under exposure to 1 x 10(-6) mbar O-2 at Pt coverages below 1.3 ML. Using NAP XPS, we observe the formation of an interfacial PtOx at high Pt coverage (2.0 ML) in an oxygen atmosphere (1 mbar) at 300 K while the formation of surface PtOx is kinetically hindered and occurs above 550 K only.

Název v anglickém jazyce

Interplay between the metal- support interaction and stability in Pt/ Co3O4(111) model catalysts

Popis výsledku anglicky

The interplay between the metal-support interaction and stability with respect to sintering has been investigated for Pt nanoparticles supported on well-ordered Co3O4(111)/Ir(100) films in UHV and under oxidizing conditions by means of synchrotron radiation photoelectron spectroscopy (SRPES) and near ambient pressure X-ray photoelectron spectroscopy (NAP XPS). The electronic metal-support interaction between Pt and Co3O4(111) associated with charge transfer results in partial reduction of Co3O4(111) yielding partially oxidized Pt+ species at the interface. The stability of the supported Pt particles is coupled with the oxidation state of Pt+ species, which can be reduced or oxidized depending on the Pt coverage and reactive environment. Annealing of Pt/Co3O4(111)/Ir(100) in UHV triggers the reduction of Pt+ species. At higher temperature, reverse spillover of oxygen to the Pt nanoparticles is accompanied by reduction of Co3O4(111). Under these conditions, the oxidation state of Pt+ species depends strongly on Pt coverage. Thus, at low Pt coverage (0.3 ML Pt), Pt+ is converted to Pt4+, at intermediate coverage (1.3 ML Pt), Pt+ remains stable, and at high Pt coverage (1.93 ML), Pt+ is reduced to Pt-0. Sintering of Pt particles is associated with the reduction of the Pt+ species. This process is prevented under oxidizing conditions due to the formation of an interfacial oxide PtOx. The formation of an interfacial PtOx is observed at 300 K under exposure to 1 x 10(-6) mbar O-2 at Pt coverages below 1.3 ML. Using NAP XPS, we observe the formation of an interfacial PtOx at high Pt coverage (2.0 ML) in an oxygen atmosphere (1 mbar) at 300 K while the formation of surface PtOx is kinetically hindered and occurs above 550 K only.

Druh

J_imp - Článek v periodiku v databázi Web of Science

CEP obor

—

OECD FORD obor

10305 - Fluids and plasma physics (including surface physics)

Projekt

Výsledek vznikl pri realizaci vícero projektů. Více informací v záložce Projekty.

Návaznosti

P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)<br>S - Specificky vyzkum na vysokych skolach<br>I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Rok uplatnění

2018

Kód důvěrnosti údajů

S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Název periodika

Journal of Materials Chemistry A

ISSN

2050-7488

e-ISSN

—

Svazek periodika

6

Číslo periodika v rámci svazku

45

Stát vydavatele periodika

GB - Spojené království Velké Británie a Severního Irska

Počet stran výsledku

9

Strana od-do

23078-23086

Kód UT WoS článku

000451738200074

EID výsledku v databázi Scopus

2-s2.0-85057061637