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      Hierarchical Architectural Structures Induce High Performance in n‐Type GeTe‐Based Thermoelectrics

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          Abstract

          Compatible p‐ and n‐type materials are necessary for high‐performance GeTe thermoelectric modules, where the n‐type counterparts are in urgent need. Here, it is reported that the p‐type GeTe can be tuned into n‐type by decreasing the formation energy of Te vacancies via AgBiTe 2 alloying. AgBiTe 2 alloying induces Ag 2Te precipitates and tunes the carrier concentration close to the optimal level, leading to a high‐power factor of 6.2 µW cm −1 K −2 at 423 K. Particularly, the observed hierarchical architectural structures, including phase boundaries, nano‐precipitates, and point defects, contribute an ultralow lattice thermal conductivity of 0.39 W m −1 K −1 at 423 K. Correspondingly, an increased ZT of 0.5 at 423 K is observed in n‐type (GeTe) 0.45(AgBiTe 2) 0.55. Furthermore, a single‐leg module demonstrates a maximum η of 6.6% at the temperature range from 300 to 500 K. This study indicates that AgBiTe 2 alloying can successfully turn GeTe into n‐type with simultaneously optimized thermoelectric performance.

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          Most cited references38

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          Rationally Designing High-Performance Bulk Thermoelectric Materials.

          There has been a renaissance of interest in exploring highly efficient thermoelectric materials as a possible route to address the worldwide energy generation, utilization, and management. This review describes the recent advances in designing high-performance bulk thermoelectric materials. We begin with the fundamental stratagem of achieving the greatest thermoelectric figure of merit ZT of a given material by carrier concentration engineering, including Fermi level regulation and optimum carrier density stabilization. We proceed to discuss ways of maximizing ZT at a constant doping level, such as increase of band degeneracy (crystal structure symmetry, band convergence), enhancement of band effective mass (resonant levels, band flattening), improvement of carrier mobility (modulation doping, texturing), and decrease of lattice thermal conductivity (synergistic alloying, second-phase nanostructuring, mesostructuring, and all-length-scale hierarchical architectures). We then highlight the decoupling of the electron and phonon transport through coherent interface, matrix/precipitate electronic bands alignment, and compositionally alloyed nanostructures. Finally, recent discoveries of new compounds with intrinsically low thermal conductivity are summarized, where SnSe, BiCuSeO, MgAgSb, complex copper and bismuth chalcogenides, pnicogen-group chalcogenides with lone-pair electrons, and tetrahedrites are given particular emphasis. Future possible strategies for further enhancing ZT are considered at the end of this review.
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            Realizing high figure of merit in heavy-band p-type half-Heusler thermoelectric materials

            Solid-state thermoelectric technology offers a promising solution for converting waste heat to useful electrical power. Both high operating temperature and high figure of merit zT are desirable for high-efficiency thermoelectric power generation. Here we report a high zT of ∼1.5 at 1,200 K for the p-type FeNbSb heavy-band half-Heusler alloys. High content of heavier Hf dopant simultaneously optimizes the electrical power factor and suppresses thermal conductivity. Both the enhanced point-defect and electron–phonon scatterings contribute to a significant reduction in the lattice thermal conductivity. An eight couple prototype thermoelectric module exhibits a high conversion efficiency of 6.2% and a high power density of 2.2 W cm−2 at a temperature difference of 655 K. These findings highlight the optimization strategy for heavy-band thermoelectric materials and demonstrate a realistic prospect of high-temperature thermoelectric modules based on half-Heusler alloys with low cost, excellent mechanical robustness and stability.
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              Low-Symmetry Rhombohedral GeTe Thermoelectrics

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                Author and article information

                Contributors
                (View ORCID Profile)
                (View ORCID Profile)
                Journal
                Advanced Functional Materials
                Adv Funct Materials
                Wiley
                1616-301X
                1616-3028
                April 2023
                January 05 2023
                April 2023
                : 33
                : 14
                Affiliations
                [1 ] State Key Laboratory of Materials‐Oriented Chemical Engineering, College of Chemical Engineering Nanjing Tech University Nanjing 210009 China
                [2 ] Australian Institute for Bioengineering and Nanotechnology The University of Queensland Brisbane QLD 4072 Australia
                [3 ] School of Chemistry and Physics Queensland University of Technology Brisbane QLD 4000 Australia
                [4 ] Beijing Key Lab of Microstructure and Property of Solids Institute of Microstructure and Properties of Advanced Materials Beijing University of Technology Beijing 100124 China
                [5 ] College of Materials Science and Engineering Nanjing Tech University Nanjing 211816 China
                [6 ] School of Materials Science and Engineering Nanjing University of Science & Technology Nanjing 210094 China
                Article
                10.1002/adfm.202213040
                21de699d-28b4-4bf2-878a-8af2eddf7256
                © 2023

                http://creativecommons.org/licenses/by-nc-nd/4.0/

                http://creativecommons.org/licenses/by-nc-nd/4.0/

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