Elemental tellurium exhibits a promising thermoelectric performance, largely due to the optimization of the carrier concentration stemming from effective chemical doping. In this study, we demonstrate a novel approach to realize the collaborative manipulation of the electrical and thermal transport properties in the Te system via introduction of SbSe. A series of p-type Te(SbSe) (0 ≤ ≤ 0.2) samples were fabricated through the melting method followed by spark plasma sintering. Electrically, antimony as a successful dopant enables a remarkable improvement of the carrier concentration, from ∼10 to ∼10 cm, thus resulting in a desired power factor across the entire temperature range. Thermally, utilization of defects engineering containing point defects, grain boundaries, dislocations, and secondary phase precipitates effectively reduces the lattice thermal conductivity. The coexistence of multi-frequency phonon scattering centers derived from the addition of SbSe leads to a minimum lattice thermal conductivity of 0.5 W m K, approaching the amorphous limit. As a result, Te(SbSe) shows the highest figure of merit ZT ∼1 at 600 K, comparable to that of the toxic Te(As) thermoelectrics. This work not only points out that synergistic effects of both doping and defect engineering play a vital role in decoupling the thermoelectric parameters in the Te(SbSe) system but also gives a referential strategy for a higher thermoelectric performance in other Te-based materials.
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Sci Rep
December 2024
Centre Énergie, Matériaux Télécommunications, Institut National de la Recherche Scientifique, 1650, Blvd, Lionel-Boulet, Varennes, QC, J3X-1P7, Canada.
RF-sputtering is used to deposit TiO-Magneli-phase films onto various substrates at deposition temperatures (T) ranging from 25 to 650 °C. Not only the structural, but also electrical conductivity, optical absorbance and photothermal properties of the TiO films are shown to change significantly with T. A T of 500 °C is pointed out as the optimal temperature that yields highly-crystalized pure-TiO-Magneli phase with a densely-packed morphology and a conductivity as high as 740 S/cm.
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December 2024
Department of Mechanical Engineering, Delhi Skill and Entrepreneurship University, Delhi, 110089, India.
This study explores the thermal conductivity and viscosity of water-based nanofluids containing silicon dioxide, graphene oxide, titanium dioxide, and their hybrids across various concentrations (0 to 1 vol%) and temperatures (30 to 60 °C). The nanofluids, characterized using multiple methods, exhibited increased viscosity and thermal conductivity compared to water, with hybrid nanofluids showing superior performance. Graphene oxide nanofluids displayed the highest thermal conductivity and viscosity ratios, with increases of 52% and 177% at 60 °C and 30 °C, respectively, for a concentration of 1 vol% compared to base fluid.
View Article and Find Full Text PDFACS Appl Mater Interfaces
December 2024
Institute of Chemical Engineering Sciences, Foundation of Research and Technology- Hellas (FORTH/ICE-HT), Stadiou Street, Platani, Patras 26504, Greece.
Due to their outstanding electrical and thermal properties, graphene and related materials have been proposed as ideal candidates for the development of lightweight systems for thermoelectric applications. Recently, the nanolaminate architecture that entails alternation of continuous graphene monolayers and ultrathin polymer films has been proposed as an efficient route for the development of composites with impressive physicochemical properties. In this work, we present a novel layer-by-layer approach for the fabrication of highly ordered, flexible, heat-resistant, and electrically conductive freestanding graphene/polymer nanolaminates through alternating Marangoni-driven self-assembly of reduced graphene oxide (rGO) and poly(ether imide) (PEI) films.
View Article and Find Full Text PDFMembranes (Basel)
December 2024
LIME Laboratory, CNRS, MADIREL (UMR 7246), Campus St Jérôme, Aix Marseille University, 13013 Marseille, France.
Anion Exchange Membranes (AEMs) are promising materials for electrochemical devices, such as fuel cells and electrolyzers. However, the main drawback of AEMs is their low durability in alkaline operating conditions. A possible solution is the use of composite ionomers containing inorganic fillers stable in a basic environment.
View Article and Find Full Text PDFMembranes (Basel)
December 2024
Unit of Chemical Technologies, Technology Centre of Catalonia, Eurecat, 43007 Tarragona, Spain.
The urgent need for sustainable, low-emission energy solutions has positioned proton exchange membrane fuel cells (PEMFCs) as a promising technology in clean energy conversion. Polysulfone (PSF) membranes with incorporated ionic liquid (IL) and hydrophobic polydimethylsiloxane-functionalized silica (SiO-PDMS) were developed and characterized for their potential application in PEMFCs. Using a phase inversion method, membranes with various combinations of PSFs, SiO-PDMS, and 1-butyl-3-methylimidazolium triflate (BMI.
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