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      Arsenic-Doped SnSe Thin Films Prepared by Pulsed Laser Deposition

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          Abstract

          Pulsed UV laser deposition was exploited for the preparation of thin Sn 50– x As x Se 50 ( x = 0, 0.05, 0.5, and 2.5) films with the aim of investigating the influence of low arsenic concentration on the properties of the deposited layers. It was found that the selected deposition method results in growth of a highly ( h00) oriented orthorhombic SnSe phase. The thin films were characterized by different techniques such as X-ray diffraction, scanning electron microscopy with energy-dispersive X-ray spectroscopy, atomic force microscopy, Raman scattering spectroscopy, and spectroscopic ellipsometry. From the results, it can be concluded that thin films containing 0.5 atom % of As exhibited extreme values regarding crystallite size, unit cell volume, or refractive index that significantly differ from those of other samples. Laser ablation with quadrupole ion trap time-of-flight mass spectrometry was used to identify and compare species present in the plasma originating from the interaction of a laser pulse with solid-state Sn 50– x As x Se 50 materials in both forms, i.e. parent powders as well as deposited thin films. The mass spectra of both materials were similar; particularly, signals of Sn m Se n + clusters with low m and n values were observed.

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          Ultralow thermal conductivity and high thermoelectric figure of merit in SnSe crystals.

          The thermoelectric effect enables direct and reversible conversion between thermal and electrical energy, and provides a viable route for power generation from waste heat. The efficiency of thermoelectric materials is dictated by the dimensionless figure of merit, ZT (where Z is the figure of merit and T is absolute temperature), which governs the Carnot efficiency for heat conversion. Enhancements above the generally high threshold value of 2.5 have important implications for commercial deployment, especially for compounds free of Pb and Te. Here we report an unprecedented ZT of 2.6 ± 0.3 at 923 K, realized in SnSe single crystals measured along the b axis of the room-temperature orthorhombic unit cell. This material also shows a high ZT of 2.3 ± 0.3 along the c axis but a significantly reduced ZT of 0.8 ± 0.2 along the a axis. We attribute the remarkably high ZT along the b axis to the intrinsically ultralow lattice thermal conductivity in SnSe. The layered structure of SnSe derives from a distorted rock-salt structure, and features anomalously high Grüneisen parameters, which reflect the anharmonic and anisotropic bonding. We attribute the exceptionally low lattice thermal conductivity (0.23 ± 0.03 W m(-1) K(-1) at 973 K) in SnSe to the anharmonicity. These findings highlight alternative strategies to nanostructuring for achieving high thermoelectric performance.
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            Phase change materials and their application to nonvolatile memories.

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              Thermoelectric properties of p-type polycrystalline SnSe doped with Ag

              Doped polycrystalline SnSe could have zT 0.6 at 750 K, suggesting good potential for thermoelectrics. Challenges come from difficulty in doping and hysteresis in resistivity.
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                Author and article information

                Journal
                ACS Omega
                ACS Omega
                ao
                acsodf
                ACS Omega
                American Chemical Society
                2470-1343
                30 June 2021
                13 July 2021
                : 6
                : 27
                : 17483-17491
                Affiliations
                []Department of Chemistry, Faculty of Science, Masaryk University , Kamenice 5/A14, 62500 Brno, Czech Republic
                []Department of Graphic Arts and Photophysics, Faculty of Chemical Technology, University of Pardubice , Studentská 573, 53210 Pardubice, Czech Republic
                [§ ]Institute of Applied Physics and Mathematics, Faculty of Chemical Technology, University of Pardubice , Studentská 573, 53210 Pardubice, Czech Republic
                []Univ Rennes, CNRS , ISCR UMR6226, ScanMAT UMS 2001, F-35000 Rennes, France
                Author notes
                [* ]Email: petr.nemec@ 123456upce.cz . Phone: +420466037247.
                Author information
                https://orcid.org/0000-0002-0113-3935
                https://orcid.org/0000-0002-6675-5671
                https://orcid.org/0000-0003-2426-3078
                Article
                10.1021/acsomega.1c01892
                8280661
                34278134
                63d1d2d8-f0cd-4ed5-ab3f-416a35553166
                © 2021 The Authors. Published by American Chemical Society

                Permits non-commercial access and re-use, provided that author attribution and integrity are maintained; but does not permit creation of adaptations or other derivative works ( https://creativecommons.org/licenses/by-nc-nd/4.0/).

                History
                : 09 April 2021
                : 17 June 2021
                Funding
                Funded by: Ministerstvo Å kolství, Mládeže a TÄ?lovýchovy, doi 10.13039/501100001823;
                Award ID: LM2018103
                Funded by: Grantová Agentura Ä?eské Republiky, doi 10.13039/501100001824;
                Award ID: 19-24516S
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                ao1c01892
                ao1c01892

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