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Exploration of Zn Resonance Levels and Thermoelectric Properties in I-Doped PbTe with ZnTe Nanostructures
Indian Institute Technology, India .
Linköpings universitet, Institutionen för fysik, kemi och biologi. Linköpings universitet, Tekniska högskolan.
Indian Institute Technology, India .
2014 (engelsk)Inngår i: ACS Applied Materials and Interfaces, ISSN 1944-8244, E-ISSN 1944-8252, Vol. 6, nr 6, s. 3995-4004Artikkel i tidsskrift (Fagfellevurdert) Published
Abstract [en]

Motivated by the theoretically predicted Zn resonant states in the conduction band of PbTe, in the present work, we investigated the effect of Zn substitution on the thermoelectric properties in I-doped n-type PbTe. The room temperature thermopower values show good agreement with the theoretical Pisarenko plot of PbTe up to a carrier concentration of 4.17 X 10(19) cm(-3); thus, the presence of Zn resonance levels is not observed. Because of the low solubility of Zn in PbTe, a second phase of coherent ZnTe nanostructures is observed within the PbTe host matrix, which is found to reduce the lattice thermal conductivity. The reduced lattice thermal conductivity in PbTe by ZnTe nanostructures leads to notable enhancement in the figure of merit with a maximum value of 1.35 at 650 K. In contrast to the recent literature, the carrier mobility is not found to be affected by the band offset between ZnTe nanostructures and PbTe. This is explained by the quantum tunneling of the charge carrier through the narrow offset barrier and depletion width and coherent nature of the interface boundary between the two phases, i.e., ZnTe and PbTe.

sted, utgiver, år, opplag, sider
American Chemical Society , 2014. Vol. 6, nr 6, s. 3995-4004
Emneord [en]
resonant states; coherent nanostructures; lattice thermal conductivity; band offset; thermoelectric figure of merit
HSV kategori
Identifikatorer
URN: urn:nbn:se:liu:diva-106287DOI: 10.1021/am405410eISI: 000333551500031OAI: oai:DiVA.org:liu-106287DiVA, id: diva2:715741
Tilgjengelig fra: 2014-05-06 Laget: 2014-05-05 Sist oppdatert: 2017-12-05

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