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In-situ preparation of Ni@ZrO<sub>2</sub> nanocapsules powder by DC arc plasma for internal electrode of MLCC

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dc.contributor.authorLi, Xi-Yang-
dc.contributor.authorQu, Xing-Hao-
dc.contributor.authorLiu, Dong-
dc.contributor.authorZhu, Guang-Yun-
dc.contributor.authorDong, Xing-Long-
dc.contributor.authorJung, Youngguan-
dc.date.accessioned2024-06-13T07:00:29Z-
dc.date.available2024-06-13T07:00:29Z-
dc.date.issued2024-06-
dc.identifier.issn0042-207X-
dc.identifier.issn1879-2715-
dc.identifier.urihttps://scholarworks.bwise.kr/kumoh/handle/2020.sw.kumoh/28683-
dc.description.abstractZirconium oxide-coated Ni nanocapsules (Ni@ZrO2 NCs) were in-situ fabricated by DC arc plasma in a nitrogen atmosphere. The co-evaporation of a target mixture consisting of coarse ZrO2 and Ni powders resulted in the formation of Ni@ZrO2 core-shell nanocomposites (NCs). The high energy states of excited ions (Ni3+, Zr4+, O2-, N2+, etc.) within the arc plasma region were recorded in real time by online optical emission spectroscopy (OES), which becomes visible evidences of the energy conditions for the fabrication of Ni@ZrO2 NCs. These nanocapsules underwent preferential formation of zirconium oxide species based on the oxygen potential rule, followed by the nucleation and subsequent growth processes. The Ni@ZrO2 NCs exhibited improved oxidation resistance, with an onset temperature for sintering approximately 40 degrees C higher than that of pristine Ni nanoparticles (NPs). Additionally, these NCs displayed an appropriate shrinkage rate, with a volume change of about 7.1% at 1200 degrees C. The symbiotic relationship between the ZrO2 shell and the Ni core within each nanoparticle suggests enhanced interfacial stability, rendering these NCs a promising material for the advancement of multilayer ceramic capacitors (MLCCs).-
dc.language영어-
dc.language.isoENG-
dc.publisherPERGAMON-ELSEVIER SCIENCE LTD-
dc.titleIn-situ preparation of Ni@ZrO&lt;sub&gt;2&lt;/sub&gt; nanocapsules powder by DC arc plasma for internal electrode of MLCC-
dc.typeArticle-
dc.publisher.location영국-
dc.identifier.doi10.1016/j.vacuum.2024.113130-
dc.identifier.scopusid2-s2.0-85188545999-
dc.identifier.wosid001216478600001-
dc.identifier.bibliographicCitationVACUUM, v.224-
dc.citation.titleVACUUM-
dc.citation.volume224-
dc.type.docTypeArticle-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaMaterials Science-
dc.relation.journalResearchAreaPhysics-
dc.relation.journalWebOfScienceCategoryMaterials Science, Multidisciplinary-
dc.relation.journalWebOfScienceCategoryPhysics, Applied-
dc.subject.keywordPlusMULTILAYER CERAMIC CAPACITORS-
dc.subject.keywordPlusENERGY DENSITY-
dc.subject.keywordPlusWATER-VAPOR-
dc.subject.keywordPlusNI-
dc.subject.keywordPlusSURFACE-
dc.subject.keywordPlusNANOPARTICLE-
dc.subject.keywordPlusDEGRADATION-
dc.subject.keywordPlusTEMPERATURE-
dc.subject.keywordPlusADSORPTION-
dc.subject.keywordPlusCONSTANT-
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