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Application of synchrotron through-the-substrate microdiffraction to crystals in polished thin sections

The synchrotron through-the-substrate X-ray microdiffraction technique (tts-μXRD) is extended to the structural study of microvolumes of crystals embedded in polished thin sections of compact materials [Rius, Labrador, Crespi, Frontera, Vallcorba & Melgarejo (2011 ▸). J.Synchrotron Rad. 18, 891–...

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Autores principales: Rius, Jordi, Vallcorba, Oriol, Frontera, Carlos, Peral, Inmaculada, Crespi, Anna, Miravitlles, Carles
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Union of Crystallography 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4491317/
https://www.ncbi.nlm.nih.gov/pubmed/26175904
http://dx.doi.org/10.1107/S2052252515007794
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author Rius, Jordi
Vallcorba, Oriol
Frontera, Carlos
Peral, Inmaculada
Crespi, Anna
Miravitlles, Carles
author_facet Rius, Jordi
Vallcorba, Oriol
Frontera, Carlos
Peral, Inmaculada
Crespi, Anna
Miravitlles, Carles
author_sort Rius, Jordi
collection PubMed
description The synchrotron through-the-substrate X-ray microdiffraction technique (tts-μXRD) is extended to the structural study of microvolumes of crystals embedded in polished thin sections of compact materials [Rius, Labrador, Crespi, Frontera, Vallcorba & Melgarejo (2011 ▸). J.Synchrotron Rad. 18, 891–898]. The resulting tts-μXRD procedure includes some basic steps: (i) collection of a limited number of consecutive two-dimensional patterns (frames) for each randomly oriented crystal microvolume; (ii) refinement of the metric from the one-dimensional diffraction pattern which results from circularly averaging the sum of collected frames; (iii) determination of the reciprocal lattice orientation of each randomly oriented crystal microvolume which allows assigning the hkl indices to the spots and, consequently, merging the intensities of the different frames into a single-crystal data set (frame merging); and (iv) merging of the individual crystal data sets (multicrystal merging) to produce an extended data set suitable for structure refinement/solution. Its viability for crystal structure solution by Patterson function direct methods (δ recycling) and for accurate single-crystal least-squares refinements is demonstrated with some representative examples from petrology in which different glass substrate thicknesses have been employed. The section of the crystal microvolume must be at least of the same order of magnitude as the focus of the beam (15 × 15 µm in the provided examples). Thanks to its versatility and experimental simplicity, this method­ology should be useful for disciplines as disparate as petrology, materials science and cultural heritage.
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spelling pubmed-44913172015-07-14 Application of synchrotron through-the-substrate microdiffraction to crystals in polished thin sections Rius, Jordi Vallcorba, Oriol Frontera, Carlos Peral, Inmaculada Crespi, Anna Miravitlles, Carles IUCrJ Feature Articles The synchrotron through-the-substrate X-ray microdiffraction technique (tts-μXRD) is extended to the structural study of microvolumes of crystals embedded in polished thin sections of compact materials [Rius, Labrador, Crespi, Frontera, Vallcorba & Melgarejo (2011 ▸). J.Synchrotron Rad. 18, 891–898]. The resulting tts-μXRD procedure includes some basic steps: (i) collection of a limited number of consecutive two-dimensional patterns (frames) for each randomly oriented crystal microvolume; (ii) refinement of the metric from the one-dimensional diffraction pattern which results from circularly averaging the sum of collected frames; (iii) determination of the reciprocal lattice orientation of each randomly oriented crystal microvolume which allows assigning the hkl indices to the spots and, consequently, merging the intensities of the different frames into a single-crystal data set (frame merging); and (iv) merging of the individual crystal data sets (multicrystal merging) to produce an extended data set suitable for structure refinement/solution. Its viability for crystal structure solution by Patterson function direct methods (δ recycling) and for accurate single-crystal least-squares refinements is demonstrated with some representative examples from petrology in which different glass substrate thicknesses have been employed. The section of the crystal microvolume must be at least of the same order of magnitude as the focus of the beam (15 × 15 µm in the provided examples). Thanks to its versatility and experimental simplicity, this method­ology should be useful for disciplines as disparate as petrology, materials science and cultural heritage. International Union of Crystallography 2015-06-11 /pmc/articles/PMC4491317/ /pubmed/26175904 http://dx.doi.org/10.1107/S2052252515007794 Text en © Jordi Rius et al. 2015 http://creativecommons.org/licenses/by/2.0/uk/ This is an open-access article distributed under the terms of the Creative Commons Attribution Licence, which permits unrestricted use, distribution, and reproduction in any medium, provided the original authors and source are cited.
spellingShingle Feature Articles
Rius, Jordi
Vallcorba, Oriol
Frontera, Carlos
Peral, Inmaculada
Crespi, Anna
Miravitlles, Carles
Application of synchrotron through-the-substrate microdiffraction to crystals in polished thin sections
title Application of synchrotron through-the-substrate microdiffraction to crystals in polished thin sections
title_full Application of synchrotron through-the-substrate microdiffraction to crystals in polished thin sections
title_fullStr Application of synchrotron through-the-substrate microdiffraction to crystals in polished thin sections
title_full_unstemmed Application of synchrotron through-the-substrate microdiffraction to crystals in polished thin sections
title_short Application of synchrotron through-the-substrate microdiffraction to crystals in polished thin sections
title_sort application of synchrotron through-the-substrate microdiffraction to crystals in polished thin sections
topic Feature Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4491317/
https://www.ncbi.nlm.nih.gov/pubmed/26175904
http://dx.doi.org/10.1107/S2052252515007794
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