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Study of active surface centers of Pt/CeO2 catalysts prepared using radio-frequency plasma sputtering technique. / Stadnichenko, Andrey I.; Muravev, Valerii V.; Koscheev, Sergey V. и др.

в: Surface Science, Том 679, 01.01.2019, стр. 273-283.

Результаты исследований: Научные публикации в периодических изданияхстатьяРецензирование

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Stadnichenko AI, Muravev VV, Koscheev SV, Zaikovskii VI, Aleksandrov HA, Neyman KM и др. Study of active surface centers of Pt/CeO2 catalysts prepared using radio-frequency plasma sputtering technique. Surface Science. 2019 янв. 1;679:273-283. doi: 10.1016/j.susc.2018.10.002

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Stadnichenko, Andrey I. ; Muravev, Valerii V. ; Koscheev, Sergey V. и др. / Study of active surface centers of Pt/CeO2 catalysts prepared using radio-frequency plasma sputtering technique. в: Surface Science. 2019 ; Том 679. стр. 273-283.

BibTeX

@article{7df796959e164256a837861a6bddc913,
title = "Study of active surface centers of Pt/CeO2 catalysts prepared using radio-frequency plasma sputtering technique",
abstract = "RF-plasma deposition of Pt on a nanosized ceria powder support has been performed directly in photoelectron spectrometer chambers to prepare model catalysts. The plasma deposition in an oxidizing environment results in the formation of highly dispersed oxide nanoparticles up to 2 nm large, which contain platinum solely as Pt4+ ions revealed by Eb(Pf4f7/2) = 74.6 eV. Thus prepared model catalyst samples arranged as (sub-monolayer) films of PtO2 nanoparticles on the surface of CeO2 are characterized by an increased thermal stability compared with PtO2 nanoparticles deposited on more inert supports. These PtO2/CeO2 model catalysts show a high activity in the CO oxidation even at room temperature. A detailed analysis of the O1s spectra obtained during the titration by CO of PtO2/CeO2 films strongly suggests that the reactive oxygen species are manifested with Eb(O1s) = 530.8 eV and 532.9 eV. The latter core level energies are attributed to oxygen in the platinum dioxide and to peroxide-like oxygen, presumably located at the interface between PtO2 and CeO2 particles. Results of our density-functional calculations indicate that the peroxide-like species can be energetically stabilized at the PtOx–CeO2 interfaces.",
keywords = "Ceria, CO oxidation, DFT calculations, Oxygen species, Platinum, RF-plasma sputtering, XPS, THERMAL-STABILITY, THIN-FILMS, OXIDE, CO OXIDATION, AL2O3 FILMS, REACTION PROBABILITY, RAY PHOTOELECTRON-SPECTROSCOPY, PLATINUM NANOPARTICLES, CERIA, IN-SITU",
author = "Stadnichenko, {Andrey I.} and Muravev, {Valerii V.} and Koscheev, {Sergey V.} and Zaikovskii, {Vladimir I.} and Aleksandrov, {Hristiyan A.} and Neyman, {Konstantin M.} and Boronin, {Andrei I.}",
year = "2019",
month = jan,
day = "1",
doi = "10.1016/j.susc.2018.10.002",
language = "English",
volume = "679",
pages = "273--283",
journal = "Surface Science",
issn = "0039-6028",
publisher = "Elsevier",

}

RIS

TY - JOUR

T1 - Study of active surface centers of Pt/CeO2 catalysts prepared using radio-frequency plasma sputtering technique

AU - Stadnichenko, Andrey I.

AU - Muravev, Valerii V.

AU - Koscheev, Sergey V.

AU - Zaikovskii, Vladimir I.

AU - Aleksandrov, Hristiyan A.

AU - Neyman, Konstantin M.

AU - Boronin, Andrei I.

PY - 2019/1/1

Y1 - 2019/1/1

N2 - RF-plasma deposition of Pt on a nanosized ceria powder support has been performed directly in photoelectron spectrometer chambers to prepare model catalysts. The plasma deposition in an oxidizing environment results in the formation of highly dispersed oxide nanoparticles up to 2 nm large, which contain platinum solely as Pt4+ ions revealed by Eb(Pf4f7/2) = 74.6 eV. Thus prepared model catalyst samples arranged as (sub-monolayer) films of PtO2 nanoparticles on the surface of CeO2 are characterized by an increased thermal stability compared with PtO2 nanoparticles deposited on more inert supports. These PtO2/CeO2 model catalysts show a high activity in the CO oxidation even at room temperature. A detailed analysis of the O1s spectra obtained during the titration by CO of PtO2/CeO2 films strongly suggests that the reactive oxygen species are manifested with Eb(O1s) = 530.8 eV and 532.9 eV. The latter core level energies are attributed to oxygen in the platinum dioxide and to peroxide-like oxygen, presumably located at the interface between PtO2 and CeO2 particles. Results of our density-functional calculations indicate that the peroxide-like species can be energetically stabilized at the PtOx–CeO2 interfaces.

AB - RF-plasma deposition of Pt on a nanosized ceria powder support has been performed directly in photoelectron spectrometer chambers to prepare model catalysts. The plasma deposition in an oxidizing environment results in the formation of highly dispersed oxide nanoparticles up to 2 nm large, which contain platinum solely as Pt4+ ions revealed by Eb(Pf4f7/2) = 74.6 eV. Thus prepared model catalyst samples arranged as (sub-monolayer) films of PtO2 nanoparticles on the surface of CeO2 are characterized by an increased thermal stability compared with PtO2 nanoparticles deposited on more inert supports. These PtO2/CeO2 model catalysts show a high activity in the CO oxidation even at room temperature. A detailed analysis of the O1s spectra obtained during the titration by CO of PtO2/CeO2 films strongly suggests that the reactive oxygen species are manifested with Eb(O1s) = 530.8 eV and 532.9 eV. The latter core level energies are attributed to oxygen in the platinum dioxide and to peroxide-like oxygen, presumably located at the interface between PtO2 and CeO2 particles. Results of our density-functional calculations indicate that the peroxide-like species can be energetically stabilized at the PtOx–CeO2 interfaces.

KW - Ceria

KW - CO oxidation

KW - DFT calculations

KW - Oxygen species

KW - Platinum

KW - RF-plasma sputtering

KW - XPS

KW - THERMAL-STABILITY

KW - THIN-FILMS

KW - OXIDE

KW - CO OXIDATION

KW - AL2O3 FILMS

KW - REACTION PROBABILITY

KW - RAY PHOTOELECTRON-SPECTROSCOPY

KW - PLATINUM NANOPARTICLES

KW - CERIA

KW - IN-SITU

UR - http://www.scopus.com/inward/record.url?scp=85054784501&partnerID=8YFLogxK

U2 - 10.1016/j.susc.2018.10.002

DO - 10.1016/j.susc.2018.10.002

M3 - Article

AN - SCOPUS:85054784501

VL - 679

SP - 273

EP - 283

JO - Surface Science

JF - Surface Science

SN - 0039-6028

ER -

ID: 17115818