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Improvement in the thermoelectric performance of highly reproducible n-type (Bi,Sb)(2)Se(3)alloys by Cl-doping

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dc.contributor.authorNasir, Nadra-
dc.contributor.authorLee, Kyu Hyoung-
dc.contributor.authorKim, Sang-il-
dc.contributor.authorKim, Hyun-Sik-
dc.contributor.authorLim, Jae-Hong-
dc.contributor.authorFu, Liangwei-
dc.contributor.authorKim, Sung Wng-
dc.date.available2021-03-17T06:53:04Z-
dc.date.created2021-02-26-
dc.date.issued2020-06-
dc.identifier.issn2046-2069-
dc.identifier.urihttps://scholarworks.bwise.kr/hongik/handle/2020.sw.hongik/11677-
dc.description.abstract(Bi,Sb)(2)Se(3)alloys are promising alternatives to commercial n-type Bi-2(Te,Se)(3)ingots for low-mid temperature thermoelectric power generation due to their high thermoelectric conversion efficiency at elevated temperatures. Herein, we report the enhanced high-temperature thermoelectric performance of the polycrystalline Cl-doped Bi2-xSbxSe3(x= 0.8, 1.0) bulks and their sustainable thermal stability. Significant role of Cl substitution, characterized to enhance the power factor and reduce the thermal conductivity synergetically, is clearly elucidated. Cl-doping at Se-site of both Bi(1.2)Sb(0.8)Se(3)and BiSbSe(3)results in a high power factor by carrier generation and Hall mobility improvement while maintaining converged electronic band valleys. Furthermore, point defect phonon scattering originated from mass fluctuations formed at Cl-substituted Se-sites reduces the lattice thermal conductivity. Most importantly, spark plasma sintered Cl-doped Bi(2-x)Sb(x)Se(3)bulks are thermally stable up to 700 K, and show a reproducible maximum thermoelectric figure of merit,zT, of 0.68 at 700 K.-
dc.publisherROYAL SOC CHEMISTRY-
dc.titleImprovement in the thermoelectric performance of highly reproducible n-type (Bi,Sb)(2)Se(3)alloys by Cl-doping-
dc.typeArticle-
dc.contributor.affiliatedAuthorKim, Hyun-Sik-
dc.identifier.doi10.1039/d0ra04065g-
dc.identifier.scopusid2-s2.0-85087543299-
dc.identifier.wosid000544898700056-
dc.identifier.bibliographicCitationRSC ADVANCES, v.10, no.41, pp.24663 - 24668-
dc.relation.isPartOfRSC ADVANCES-
dc.citation.titleRSC ADVANCES-
dc.citation.volume10-
dc.citation.number41-
dc.citation.startPage24663-
dc.citation.endPage24668-
dc.type.rimsART-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaChemistry-
dc.relation.journalWebOfScienceCategoryChemistry, Multidisciplinary-
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