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Characterization of Electron Donor Sites on Al2O3 Surface Full article

Journal PCCP: Physical Chemistry Chemical Physics
ISSN: 1463-9076 , E-ISSN: 1463-9084
Output data Year: 2012, Volume: 14, Pages: 2587-2598 Pages count : 12 DOI: 10.1039/c2cp20863f
Tags RADICAL-ANIONS; SPIN-RESONANCE; CATION-RADICALS; ACID SITES; ALUMINA; GENERATION; ESR; DECOMPOSITION; MgO; SPECTROSCOPY
Authors Medvedev Dmitrii A. 1 , Rybinskaya Alexandra A. 1,2 , Kenzhin Roman M. 1 , Volodin Alexander M. 1 , Bedilo Alexander F. 1
Affiliations
1 Boreskov Institute of Catalysis, Prospekt Lavrentieva 5, Novosibirsk 630090, Russia
2 Institute of Inorganic Chemistry, Prospekt Lavrentieva 3, Novosibirsk 630090, Russia.

Funding (1)

1 Russian Foundation for Basic Research 10-03-00691

Abstract: Formation of radical anions after adsorption of 1,3,5-trinitrobenzene (TNB) on electron donor sites of fully oxidized Al2O3 samples with different phase compositions is studied by EPR. It is shown that the maximum concentration of the radical anions does not substantially depend on the choice of solvent and reaction temperature, and can be used to measure the total concentration of the donor sites. The donor sites are observed in almost the same concentration about 5 × 1016 m−2 on all alumina polymorphs except for α-Al2O3. The formation rate of the TNB radical anions and the activation energy of this process are found to depend on the donor properties of the solvent. The EPRin situ experiments showed that a substantial amount of the adsorbate forming a liquid phase is required for generation of the radical anions. These results prove that the sites measured by the formation of the TNB radical anions are not genuine electron donor sites capable of direct electron transfer to the adsorbed TNB molecules. A model of the observed paramagnetic species based on the obtained experimental data and the results of quantum chemical simulations is suggested. According to this model, a TNB radical anion substitutes a hydroxyl group forming a neutral ion pair with a surface aluminum cation. The suggested mechanism for the formation of such ion pairs involves the migration of simple radicals and does not require long-distance charge separation. It is supposed that the donor site where the process is initiated includes a negatively charged surface hydroxyl group.
Cite: Medvedev D.A. , Rybinskaya A.A. , Kenzhin R.M. , Volodin A.M. , Bedilo A.F.
Characterization of Electron Donor Sites on Al2O3 Surface
PCCP: Physical Chemistry Chemical Physics. 2012. V.14. P.2587-2598. DOI: 10.1039/c2cp20863f WOS Scopus РИНЦ ANCAN PMID OpenAlex
Dates:
Submitted: Mar 22, 2011
Accepted: Dec 2, 2011
Published online: Jan 23, 2012
Identifiers:
Web of science: WOS:000299742000006
Scopus: 2-s2.0-84856930786
Elibrary: 17976628
Chemical Abstracts: 2012:155776
Chemical Abstracts (print): 156:214864
PMID: 22267180
OpenAlex: W1991869781
Citing:
DB Citing
Web of science 42
Scopus 45
OpenAlex 54
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