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Growth of Ca2MnO4 Ruddlesden-Popper structured thin films using Combinatorial Substrate Epitaxy

Identifieur interne : 000720 ( Main/Exploration ); précédent : 000719; suivant : 000721

Growth of Ca2MnO4 Ruddlesden-Popper structured thin films using Combinatorial Substrate Epitaxy

Auteurs : Morgane Lacotte [France] ; Adrien David [France] ; Dhanapal Pravarthana [France] ; Clara Grygiel [France] ; Gregory S. Rohrer [États-Unis] ; Paul A. Salvador [États-Unis] ; Matias Velázquez [France] ; K. De Kloe [Pays-Bas] ; Wilfrid Prellier [France]

Source :

RBID : Hal:hal-01101849

Abstract

The local epitaxial growth of pulsed laser deposited Ca$_2$MnO$_4$ films on polycrystalline spark plasma sintered Sr$_2$TiO$_4$ substrates was investigated to determine phase formation and preferred epitaxial orientation relationships ($ORs$) for isostructural Ruddlesden-Popper (RP) heteroepitaxy, further developing the high-throughput synthetic approach called Combinatorial Substrate Epitaxy (CSE). Both grazing incidence X-ray diffraction and electron backscatter diffraction (EBSD) patterns of the film and substrate were indexable as single-phase RP-structured compounds. The optimal growth temperature (between 650 $^{\circ}$C and 800 $^{\circ}$C) was found to be 750 $^{\circ}$C using the maximum value of the average image quality (IQ) of the backscattered diffraction patterns. Films grew in a grain-over-grain pattern such that each Ca$_2$MnO$_4$ grain had a single $OR$ with the Sr$_2$TiO$_4$ grain on which it grew. Three primary $ORs$ described 47 out of 49 grain pairs that covered nearly all of RP orientation space. The first $OR$, found for 20 of the 49, was the expected RP unit-cell over RP unit-cell $OR$, expressed as [100][001]$_{film}$||[100][001]$_{sub}$. The other two $ORs$ were essentially rotated from the first by 90$^{\circ}$, with one (observed for 17 of 49 pairs) being rotated about the [100] and the other (observed for 10 of 49 pairs) being rotated about the [110] (and not exactly by 90$^{\circ}$). These results indicate that only a small number of $ORs$ are needed to describe isostructural RP heteroepitaxy and further demonstrate the potential of CSE in the design and growth of a wide range of complex functional oxides.

Url:
DOI: 10.1063/1.4905012


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<orgName>Université de Caen Normandie</orgName>
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<addrLine>Esplanade de la Paix - CS 14032 - 14032 CAEN Cedex 5</addrLine>
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<country>France</country>
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<idno type="DOI">10.1063/1.4905012</idno>
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<title level="j">Journal of Applied Physics</title>
<idno type="ISSN">0021-8979</idno>
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<date type="datePub">2014</date>
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<div type="abstract" xml:lang="en">The local epitaxial growth of pulsed laser deposited Ca$_2$MnO$_4$ films on polycrystalline spark plasma sintered Sr$_2$TiO$_4$ substrates was investigated to determine phase formation and preferred epitaxial orientation relationships ($ORs$) for isostructural Ruddlesden-Popper (RP) heteroepitaxy, further developing the high-throughput synthetic approach called Combinatorial Substrate Epitaxy (CSE). Both grazing incidence X-ray diffraction and electron backscatter diffraction (EBSD) patterns of the film and substrate were indexable as single-phase RP-structured compounds. The optimal growth temperature (between 650 $^{\circ}$C and 800 $^{\circ}$C) was found to be 750 $^{\circ}$C using the maximum value of the average image quality (IQ) of the backscattered diffraction patterns. Films grew in a grain-over-grain pattern such that each Ca$_2$MnO$_4$ grain had a single $OR$ with the Sr$_2$TiO$_4$ grain on which it grew. Three primary $ORs$ described 47 out of 49 grain pairs that covered nearly all of RP orientation space. The first $OR$, found for 20 of the 49, was the expected RP unit-cell over RP unit-cell $OR$, expressed as [100][001]$_{film}$||[100][001]$_{sub}$. The other two $ORs$ were essentially rotated from the first by 90$^{\circ}$, with one (observed for 17 of 49 pairs) being rotated about the [100] and the other (observed for 10 of 49 pairs) being rotated about the [110] (and not exactly by 90$^{\circ}$). These results indicate that only a small number of $ORs$ are needed to describe isostructural RP heteroepitaxy and further demonstrate the potential of CSE in the design and growth of a wide range of complex functional oxides.</div>
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<li>France</li>
<li>Pays-Bas</li>
<li>États-Unis</li>
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<li>Aquitaine</li>
<li>Nouvelle-Aquitaine</li>
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<li>Bordeaux</li>
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<name sortKey="Pravarthana, Dhanapal" sort="Pravarthana, Dhanapal" uniqKey="Pravarthana D" first="Dhanapal" last="Pravarthana">Dhanapal Pravarthana</name>
<name sortKey="Prellier, Wilfrid" sort="Prellier, Wilfrid" uniqKey="Prellier W" first="Wilfrid" last="Prellier">Wilfrid Prellier</name>
<name sortKey="Velazquez, Matias" sort="Velazquez, Matias" uniqKey="Velazquez M" first="Matias" last="Velázquez">Matias Velázquez</name>
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<name sortKey="De Kloe, K" sort="De Kloe, K" uniqKey="De Kloe K" first="K." last="De Kloe">K. De Kloe</name>
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