<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>6(50)</volume><submitter>Beiranvand A</submitter><funding>Varsinais-Suomen Rahasto</funding><funding>V??in?? ja Laina Kiven S????ti??</funding><pubmed_abstract>The evolution of lattice strain on crystallographic domain structures and magnetic properties of epitaxial low-bandwidth manganite Gd&lt;sub>0.6&lt;/sub>Ca&lt;sub>0.4&lt;/sub>MnO&lt;sub>3&lt;/sub> (GCMO) films have been studied with films on different substrates: SrTiO&lt;sub>3&lt;/sub>, (LaAlO&lt;sub>3&lt;/sub>)&lt;sub>0.3&lt;/sub>(Sr&lt;sub>2&lt;/sub>AlTaO&lt;sub>6&lt;/sub>)&lt;sub>0.7&lt;/sub>, SrLaAlO&lt;sub>3&lt;/sub>, and MgO. The X-ray diffraction data reveals that all of the films, except the films on MgO, are epitaxial and have an orthorhombic structure. Cross-sectional transmission electron microscopy (TEM) shows lattice mismatch-dependent microstructural defects. Large-enough tensile strain can increase oxygen vacancies concentration near the interface and can induce vacancies in the substrate. In addition, a second phase was observed in the films with tensile strain. However, compressive strain causes dislocations in the interface and a mosaic domain structure. On the other hand, the magnetic properties of the films, including saturation magnetization, coercive field, and transport property depend systematically on the substrate-induced strain. Based on these results, the choice of appropriate substrate is an important key to obtaining high-quality GCMO film, which can affect the functionality of potential device applications.</pubmed_abstract><journal>ACS omega</journal><pagination>34572-34579</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8697384</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Strain-Induced Domain Structure and Its Impact on Magnetic and Transport Properties of Gd&lt;sub>0.6&lt;/sub>Ca&lt;sub>0.4&lt;/sub>MnO&lt;sub>3&lt;/sub> Thin Films.</pubmed_title><pmcid>PMC8697384</pmcid><pubmed_authors>Rivasto E</pubmed_authors><pubmed_authors>Huhtinen H</pubmed_authors><pubmed_authors>Paturi P</pubmed_authors><pubmed_authors>Beiranvand A</pubmed_authors></additional><is_claimable>false</is_claimable><name>Strain-Induced Domain Structure and Its Impact on Magnetic and Transport Properties of Gd&lt;sub>0.6&lt;/sub>Ca&lt;sub>0.4&lt;/sub>MnO&lt;sub>3&lt;/sub> Thin Films.</name><description>The evolution of lattice strain on crystallographic domain structures and magnetic properties of epitaxial low-bandwidth manganite Gd&lt;sub>0.6&lt;/sub>Ca&lt;sub>0.4&lt;/sub>MnO&lt;sub>3&lt;/sub> (GCMO) films have been studied with films on different substrates: SrTiO&lt;sub>3&lt;/sub>, (LaAlO&lt;sub>3&lt;/sub>)&lt;sub>0.3&lt;/sub>(Sr&lt;sub>2&lt;/sub>AlTaO&lt;sub>6&lt;/sub>)&lt;sub>0.7&lt;/sub>, SrLaAlO&lt;sub>3&lt;/sub>, and MgO. The X-ray diffraction data reveals that all of the films, except the films on MgO, are epitaxial and have an orthorhombic structure. Cross-sectional transmission electron microscopy (TEM) shows lattice mismatch-dependent microstructural defects. Large-enough tensile strain can increase oxygen vacancies concentration near the interface and can induce vacancies in the substrate. In addition, a second phase was observed in the films with tensile strain. However, compressive strain causes dislocations in the interface and a mosaic domain structure. On the other hand, the magnetic properties of the films, including saturation magnetization, coercive field, and transport property depend systematically on the substrate-induced strain. Based on these results, the choice of appropriate substrate is an important key to obtaining high-quality GCMO film, which can affect the functionality of potential device applications.</description><dates><release>2021-01-01T00:00:00Z</release><publication>2021 Dec</publication><modification>2025-04-04T20:35:21.76Z</modification><creation>2025-04-04T20:35:21.76Z</creation></dates><accession>S-EPMC8697384</accession><cross_references><pubmed>34963942</pubmed><doi>10.1021/acsomega.1c04904</doi></cross_references></HashMap>