Please use this identifier to cite or link to this item: http://hdl.handle.net/10397/117682
DC FieldValueLanguage
dc.contributorDepartment of Electrical and Electronic Engineeringen_US
dc.creatorMusah, JDen_US
dc.creatorOr, SWen_US
dc.date.accessioned2026-02-26T06:27:51Z-
dc.date.available2026-02-26T06:27:51Z-
dc.identifier.urihttp://hdl.handle.net/10397/117682-
dc.language.isoenen_US
dc.publisherAmerican Chemical Societyen_US
dc.subjectBismuth tellurideen_US
dc.subjectCo-dopingen_US
dc.subjectPhonon scatteringen_US
dc.subjectStrain engineeringen_US
dc.subjectThermoelectricsen_US
dc.titleStrain engineering in Ce-Sb co-doped Bi₂Te₃ enabling ultrahigh thermoelectric performanceen_US
dc.typeJournal/Magazine Articleen_US
dc.identifier.spage81en_US
dc.identifier.epage91en_US
dc.identifier.volume8en_US
dc.identifier.issue1en_US
dc.identifier.doi10.1021/acsaelm.5c01530en_US
dcterms.abstractWhile bismuth telluride (Bi2Te3) demonstrates excellent thermoelectric performance in p-type systems, its n-type variants are limited by the inherent conductivity-thermal conductivity trade-off. Here, we employ a dual-doping strategy that incorporates the rare earth element cerium (Ce) and antimony (Sb) to simultaneously optimize the electrical and thermal transport properties of n-type Bi2Te3. We demonstrate that Ce and Sb codoping serve as an effective electronic modifier, converting Bi2Te3 to an n-type conductor while suppressing bipolar conduction through dynamic carrier concentration tuning, achieving an enhanced peak figure of merit (zT) of ∼0.93 at 473 K in Bi2–x(CeSb)2𝑥/3Te3 (x = 0.05) through improved power factor optimization. Moreover, Sb codoping not only enhances the carrier mobility through strain compensation but also significantly reduces the lattice thermal conductivity to 0.37 W m–1 K–1 at 480 K through synergistic mass fluctuation and strain field phonon scattering. The combined effects yield a 63% enhancement in zT compared to conventional In–Sb-doped systems. Importantly, this performance enhancement is achieved through a scalable synthesis process that maintains phase purity and materials design with structural stability. As a result, the optimized Bi1.95(CeSb)0.033Te3 not only exhibits a higher peak zT value but also maintains high performance across both wearable (ΔT < 100 K) and industrial waste-heat recovery (400–500 K) temperature ranges. This work presents an approach for active strain engineering in the development of high-performance thermoelectric materials, surpassing traditional doping methods.en_US
dcterms.accessRightsembargoed accessen_US
dcterms.bibliographicCitationACS applied electronic materials, 13 Jan. 2026, v. 8, no. 1, p. 81-91en_US
dcterms.isPartOfACS applied electronic materialsen_US
dcterms.issued2026-01-13-
dc.identifier.scopus2-s2.0-105027232271-
dc.identifier.eissn2637-6113en_US
dc.description.validate202602 bcchen_US
dc.description.oaNot applicableen_US
dc.identifier.SubFormIDG001084/2026-02-
dc.description.fundingSourceOthersen_US
dc.description.fundingTextThis work was supported by the Innovation and Technology Commission of the HKSAR Government to the Hong Kong Branch of National Rail Transit Electrification and Automation Engineering Technology Research Center under Grant No. K-BBY1. The simulation supported by Dr. Venkateshwarlu Sarangi is also acknowledged.en_US
dc.description.pubStatusPublisheden_US
dc.date.embargo2026-12-30en_US
dc.description.oaCategoryGreen (AAM)en_US
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