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Integral Intensity of the EPR Signal of NO Molecules Adsorbed on Lewis Acid Sites of Oxide Systems as a Function of Surface Coverage Full article

Journal Applied Magnetic Resonance
ISSN: 0937-9347 , E-ISSN: 1613-7507
Output data Year: 2020, Volume: 51, Pages: 993–1003 Pages count : 10 DOI: 10.1007/s00723-020-01250-w
Tags ELECTRON-SPIN-RESONANCE; NITRIC-OXIDE; ADSORPTION; ZEOLITES; ESR; COMPLEXES; SPECTRA
Authors Shubin Aleksandr A. 1,2 , Volodin Alexander M. 1
Affiliations
1 Boreskov Institute of Catalysis, Pr. Lavrentieva, 5, Novosibirsk 630090, Russia
2 Novosibirsk State University, 1, Pirogova str., Novosibirsk 630090, Russia

Abstract: A simple model is proposed that semi-quantitatively explains the dependence of the EPR signal intensity of adsorbed NO molecules on the adsorption value. It is assumed that there are only two types of NO adsorption sites on each facet of the microcrystal, such that only NO molecules adsorbed on one of them are active in EPR. Within the framework of this model of lattice adsorption, it is assumed that there are Z other adsorption centers from the set under consideration that are available for the adsorption of neighboring NO molecules in the local environment of each EPR-active adsorption center. In this case, the formation of diamagnetic (NO)2 dimers containing an NO molecule adsorbed on a center active in the EPR decreases the integral intensity of the EPR signal. Analytical expressions are obtained for the dependence of the EPR signal intensity on the surface coverage. They were used to analyze experimental data on the adsorption of NO at the Lewis acid sites of sulfated zirconia. The proposed model consistently explains the results of EPR experiments.
Cite: Shubin A.A. , Volodin A.M.
Integral Intensity of the EPR Signal of NO Molecules Adsorbed on Lewis Acid Sites of Oxide Systems as a Function of Surface Coverage
Applied Magnetic Resonance. 2020. V.51. P.993–1003. DOI: 10.1007/s00723-020-01250-w WOS Scopus РИНЦ AN OpenAlex
Dates:
Submitted: Jul 19, 2020
Accepted: Aug 5, 2020
Published online: Sep 21, 2020
Published print: Oct 1, 2020
Identifiers:
Web of science: WOS:000571737500001
Scopus: 2-s2.0-85091161586
Elibrary: 45321998
Chemical Abstracts: 2020:2067248
OpenAlex: W3088344219
Citing: Пока нет цитирований
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