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Lattice strain-enhanced exsolution of nanoparticles in thin films

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dc.contributor.authorHan, Hyeon-
dc.contributor.authorPark, Jucheol-
dc.contributor.authorNam, Sang Yeol-
dc.contributor.authorKim, Kun Joong-
dc.contributor.authorChoi, Gyeong Man-
dc.contributor.authorParkin, Stuart S. P.-
dc.contributor.authorJang, Hyun Myung-
dc.contributor.authorIrvine, John T. S.-
dc.date.accessioned2024-02-27T16:31:33Z-
dc.date.available2024-02-27T16:31:33Z-
dc.date.issued2019-04-01-
dc.identifier.issn2041-1723-
dc.identifier.urihttps://scholarworks.bwise.kr/kumoh/handle/2020.sw.kumoh/28208-
dc.description.abstractNanoparticles formed on oxide surfaces are of key importance in many fields such as catalysis and renewable energy. Here, we control B-site exsolution via lattice strain to achieve a high degree of exsolution of nanoparticles in perovskite thin films: more than 1100 particles mu m(-2) with a particle size as small as similar to 5 nm can be achieved via strain control. Compressive-strained films show a larger number of exsolved particles as compared with tensile-strained films. Moreover, the strain-enhanced in situ growth of nanoparticles offers high thermal stability and coking resistance, a low reduction temperature (550 degrees C), rapid release of particles, and wide tunability. The mechanism of lattice strain-enhanced exsolution is illuminated by thermodynamic and kinetic aspects, emphasizing the unique role of the misfit-strain relaxation energy. This study provides critical insights not only into the design of new forms of nanostructures but also to applications ranging from catalysis, energy conversion/storage, nano-composites, nano-magnetism, to nano-optics.-
dc.language영어-
dc.language.isoENG-
dc.publisherNATURE PUBLISHING GROUP-
dc.titleLattice strain-enhanced exsolution of nanoparticles in thin films-
dc.typeArticle-
dc.publisher.location영국-
dc.identifier.doi10.1038/s41467-019-09395-4-
dc.identifier.wosid000462858400003-
dc.identifier.bibliographicCitationNATURE COMMUNICATIONS, v.10-
dc.citation.titleNATURE COMMUNICATIONS-
dc.citation.volume10-
dc.type.docTypeArticle-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClasssci-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaScience & Technology - Other Topics-
dc.relation.journalWebOfScienceCategoryMultidisciplinary Sciences-
dc.subject.keywordPlusOXIDE-
dc.subject.keywordPlusCATALYST-
dc.subject.keywordPlusPERFORMANCE-
dc.subject.keywordPlusNUCLEATION-
dc.subject.keywordPlusELECTRODES-
dc.subject.keywordPlusPARTICLES-
dc.subject.keywordPlusINTERFACE-
dc.subject.keywordPlusANODES-
dc.subject.keywordPlusPD-
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