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Surface Hydroxyl OH Defects of η-Al2O3 and χ-Al2O3 by Solid State NMR, XRD, and DFT Calculations

  • Dzhalil F. Khabibulin , Evgeniy Papulovskiy , Andrey S. Andreev , Aleksandr A. Shubin , Alexander M. Volodin , Galina A. Zenkovets , Dmitriy A. Yatsenko , Sergey V. Tsybulya and Olga B. Lapina EMAIL logo
Published/Copyright: October 15, 2016

Abstract

For the first time, the detailed structure of χ-Al2O3 and η-Al2O3 surface has been established by implementing the NMR crystallography approach. The surface of η-Al2O3 has been demonstrated to be formed primarily by the (111) facets, while the χ-Al2O3 surface is a combination of (111) and (110) facets. This observation supports the block model of aluminum oxides previously proposed by Tsybulya and Kryukova [S. V. Tsybulya, G. N. Kryukova, Phys. Rev. B 77 (2008) 024112.]. The additional terminal OH groups, observed experimentally and not contributing to (111) and (110) theoretical calculations, are considered to be bonded to the tetrahedral aluminum sites. Their origin is related to the junctions of crystallographic faces of spinel building blocks, being a part of discussed model. Higher content of these terminal OH groups in χ-Al2O3 is a result of more junctions in the case of its more mosaic structure compared to η-Al2O3.


Dedicated to: Kev Salikhov on the occasion of his 80th birthday.


Award Identifier / Grant number: 14-23-00037

Funding statement: Authors gratefully acknowledge the Russian Science Foundation (RSF grant 14-23-00037 “Design of functional nanomaterials: phenomena of self-assembly of 3D nanostructures and nanocomposites in oxide systems”) for the financial support.

Acknowledgement

Authors gratefully acknowledge the Russian Science Foundation (RSF grant 14-23-00037 “Design of functional nanomaterials: phenomena of self-assembly of 3D nanostructures and nanocomposites in oxide systems”) for the financial support.

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Supplemental Material:

The online version of this article (DOI: 10.1515/zpch-2016-0822) offers supplementary material, available to authorized users.


Received: 2016-6-14
Accepted: 2016-9-19
Published Online: 2016-10-15
Published in Print: 2017-4-1

©2017 Walter de Gruyter GmbH, Berlin/Boston

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