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Room Temperature Oxidation of Graphite by Nitrogen Dioxide with the Participation of Nanoparticles of Platinum Group Metals Review

Journal Kinetics and Catalysis
ISSN: 0023-1584 , E-ISSN: 1608-3210
Output data Year: 2023, Volume: 64, Number: 1, Pages: 78-93 Pages count : 16 DOI: 10.1134/S0023158423010093
Tags rhodium, palladium, platinum, highly oriented pyrolytic graphite (HOPG), NO2, X-ray photoelectron spectroscopy (XPS), scanning tunneling microscopy (STM), scanning electron microscopy (SEM)
Authors Smirnov M.Yu. 1 , Kalinkin A.V. 1 , Sorokin A.M. 1 , Salanov A.N. 1 , Bukhtiyarov V.I. 1
Affiliations
1 Boreskov Institute of Catalysis, Siberian Branch, Russian Academy of Sciences, Novosibirsk, 630090 Russia

Funding (1)

1 Ministry of Science and Higher Education of the Russian Federation 0239-2021-0002

Abstract: This paper presents a review of the results obtained in studying the room temperature interaction of NO2 with model systems prepared by vacuum deposition of platinum group metals on the surface of highly oriented pyrolytic graphite (M/HOPG, M = Pt, Pd, and Rh) at a pressure of 10-6–10-4 mbar. Particular attention was focused on establishing the chemical states of the supported metal particles and carbon support using X-ray photoelectron spectroscopy (XPS). Before treatment in NO2, the M/HOPG samples were characterized by scanning tunneling and/or scanning electron microscopy (STM and SEM, respectively). Upon interaction with NO2, supported palladium and rhodium remained in metallic states and, at the same time, exhibited catalytic activity in the oxidation of graphite. The process was accompanied by the destruction of ≥10–15 graphene layers with the penetration of metal particles deep into the carbon support. Rhodium was less active in the oxidation of graphite compared to palladium due to the filling of its surface with NO molecules arising from the dissociation of NO2. When the samples with deposited platinum were treated in NO2, the carbon support underwent minimal changes without disturbing its original structure. Platinum retained its metallic state when deposited on the surface of graphite annealed in a vacuum, and it was oxidized to PtO and PtO2 oxides on the surface activated by etching with argon ions. Based on the results obtained, a mechanism was proposed for the room temperature interaction of M/HOPG systems with NO2.
Cite: Smirnov M.Y. , Kalinkin A.V. , Sorokin A.M. , Salanov A.N. , Bukhtiyarov V.I.
Room Temperature Oxidation of Graphite by Nitrogen Dioxide with the Participation of Nanoparticles of Platinum Group Metals
Kinetics and Catalysis. 2023. V.64. N1. P.78-93. DOI: 10.1134/S0023158423010093 WOS Scopus РИНЦ ANCAN OpenAlex
Original: Смирнов М.Ю. , Калинкин А.В. , Сорокин А.М. , Саланов А.Н. , Бухтияров В.И.
Окисление графита диоксидом азота при комнатной температуре при участии наночастиц платиновых металлов
Кинетика и катализ. 2023. Т.64. №1. С.3-20. DOI: 10.31857/S0453881123010094 РИНЦ OpenAlex
Dates:
Submitted: Sep 22, 2022
Accepted: Oct 4, 2022
Published print: Feb 1, 2023
Published online: Jun 14, 2023
Identifiers:
Web of science: WOS:001010587400001
Scopus: 2-s2.0-85161995990
Elibrary: 53926816
Chemical Abstracts: 2023:1256575
Chemical Abstracts (print): 183:181951
OpenAlex: W4380550789
Citing:
DB Citing
OpenAlex 2
Scopus 1
Web of science 3
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