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DFT+U investigation of the catalytic properties of ferruginous clay.

Geatches, Dawn L. and Clark, Stewart J. and Greenwell, Hugh C. (2013) 'DFT+U investigation of the catalytic properties of ferruginous clay.', American mineralogist., 98 (1). pp. 132-140.

Abstract

The formation of fossil oil within clay minerals i.e., mineral-catalyzed decarboxylation, is a mechanism awaiting a thorough chemical explanation. To contribute to such an explanation, the study presented here investigates this mechanism at the level of first-principles, electronic structure computations, employing density functional theory (DFT plus Hubbard-U), planewaves, pseudopotentials, and periodic cells of two types of ferruginous clay minerals, specifically two types of nontronite [Fe2 (Si,Al)4O10(OH)2]. The formation of the fossil oil is modeled as a decarboxylation pathway, converting the fatty acid propionic acid, C2H5COOH to an alkane, C2H6 and the intermediate stages along this conversion pathway are represented by five configurations of interlayer species within the clay minerals. In this study, we test both the effect of the presence of iron on the theoretical stages of decarboxylation, together with the effect of two different density functionals: with and without strong correlations of the d-orbital electrons of iron. We have found that inclusion of the d-orbital electron correlations in the guise of a Hubbard parameter results in the introduction of three new intermediate configurations (one of which is potentially a new transition state), alters the location of the occupied Fermi level orbitals, and changes the band gaps of the clay mineral/interlayer species composites, all of which serves to inform the chemical interpretation of mineral-catalyzed decarboxylation.

Item Type:Article
Keywords:DFT, Hubbard value, Oil formation, Iron-bearing clay minerals
Full text:(AM) Accepted Manuscript
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Status:Peer-reviewed
Publisher Web site:http://dx.doi.org/10.2138/am.2013.4204
Date accepted:No date available
Date deposited:10 February 2015
Date of first online publication:January 2013
Date first made open access:No date available

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