Effects of size on the phase stability and conductivity of double-doped δ-Bi2O3

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dc.contributor.author Yasin, Polat
dc.date.accessioned 2021-05-21T07:48:05Z
dc.date.available 2021-05-21T07:48:05Z
dc.date.issued 2018-11-01
dc.identifier.citation Science Citation Index Expanded tr_TR
dc.identifier.uri https://link.springer.com/article/10.1007/s10832-018-0163-9
dc.identifier.uri http://hdl.handle.net/20.500.11787/1550
dc.description.abstract Nano and micro (Bi2O3)1-x-y(Eu2O3)x(Er2O3)y (x = 0.1, 0.15, y = 0.05, 0.2) double-doped system materials are synthesized by exploiting solid-state synthesis techniques. When we use nano sized powders to synthesize the samples we call them nano; when we use micro sized powders, we call them micro. The thermal, structural, morphological and electrical properties of nano and micro structured electrolyte samples for solid oxide fuel cells (SOFCs) are characterized. As a result of XRD measurements, the face centered δ-Bi2O3 (cubic) phase is obtained for all nano samples. However, the mixed phase is obtained for some micro samples. The electrical measurements show that conductivity decreases when the amount of Er2O3 is increased. The principal conclusion of the study is that the size effect provides relatively good structural stability in intermediate temperature SOFCs (IT SOFCs); also, the nano-Bi2O3 system has the lowest activation energy and demonstrates high electrical conductivity. tr_TR
dc.language.iso eng tr_TR
dc.publisher Springer tr_TR
dc.relation.isversionof s10832-018-0163-9 tr_TR
dc.rights info:eu-repo/semantics/closedAccess tr_TR
dc.subject IT-SOFC . Size effect . δ-Bi2O3 . Solid electrolyte . Nano-Bi2O3 tr_TR
dc.title Effects of size on the phase stability and conductivity of double-doped δ-Bi2O3 tr_TR
dc.type article tr_TR
dc.relation.journal Journal of Electroceramics tr_TR
dc.contributor.department BİLİM VE TEKNOLOJİ UYGULAMA VE ARAŞTIRMA MERKEZİ tr_TR
dc.contributor.authorID 253156 tr_TR
dc.identifier.volume 42 tr_TR
dc.identifier.startpage 89 tr_TR
dc.identifier.endpage 97 tr_TR


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