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      Electrode Effect on Ferroelectricity in Free-Standing Membranes of PbZr 0.2Ti 0.8O 3

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          Abstract

          We report the effects of screening capacity, surface roughness, and interfacial epitaxy of the bottom electrodes on the polarization switching, domain wall (DW) roughness, and ferroelectric Curie temperature ( T C) of PbZr 0.2Ti 0.8O 3 (PZT)-based free-standing membranes. Singe crystalline 10–50 nm (001) PZT and PZT/La 0.67Sr 0.33MnO 3 (LSMO) membranes are prepared on Au, correlated oxide LSMO, and two-dimensional (2D) semiconductor MoS 2 base layers. Switching the polarization of PZT yields nonvolatile current modulation in the MoS 2 channel at room temperature, with an on/off ratio of up to 2 × 10 5 and no apparent decay for more than 3 days. Piezoresponse force microscopy studies show that the coercive field E c for the PZT membranes varies from 0.75 to 3.0 MV cm –1 on different base layers and exhibits strong polarization asymmetry. The PZT/LSMO membranes exhibit significantly smaller E c, with the samples transferred on LSMO showing symmetric E c of about −0.26/+0.28 MV cm –1, smaller than that of epitaxial PZT films. The DW roughness exponent ζ points to 2D random bond disorder dominated DW roughening (ζ = 0.31) at room temperature. Upon thermal quench at progressively higher temperatures, ζ values for PZT membranes on Au and LSMO approach the theoretical value for 1D random bond disorder (ζ = 2/3), while samples on MoS 2 exhibits thermal roughening (ζ = 1/2). The PZT membranes on Au, LSMO, and MoS 2 show T C of about 763 ± 12, 725 ± 25, and 588 ± 12 °C, respectively, well exceeding the bulk value. Our study reveals the complex interplay between the electrostatic and mechanical boundary conditions in determining ferroelectricity in free-standing PZT membranes, providing important material parameters for the functional design of PZT-based flexible nanoelectronics.

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          Physics of thin-film ferroelectric oxides

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            Direct observation of ferroelectric field effect and vacancy-controlled screening at the BiFeO3/LaxSr1-xMnO3 interface.

            The development of interface-based magnetoelectric devices necessitates an understanding of polarization-mediated electronic phenomena and atomistic polarization screening mechanisms. In this work, the LSMO/BFO interface is studied on a single unit-cell level through a combination of direct order parameter mapping by scanning transmission electron microscopy and electron energy-loss spectroscopy. We demonstrate an unexpected ~5% lattice expansion for regions with negative polarization charge, with a concurrent anomalous decrease of the Mn valence and change in oxygen K-edge intensity. We interpret this behaviour as direct evidence for screening by oxygen vacancies. The vacancies are predominantly accumulated at the second atomic layer of BFO, reflecting the difference of ionic conductivity between the components. This vacancy exclusion from the interface leads to the formation of a tail-to-tail domain wall. At the same time, purely electronic screening is realized for positive polarization charge, with insignificant changes in lattice and electronic properties. These results underline the non-trivial role of electrochemical phenomena in determining the functional properties of oxide interfaces. Furthermore, these behaviours suggest that vacancy dynamics and exclusion play major roles in determining interface functionality in oxide multilayers, providing clear implications for novel functionalities in potential electronic devices.
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              Electronic transport and device prospects of monolayer molybdenum disulphide grown by chemical vapour deposition.

              Layered transition metal dichalcogenides display a wide range of attractive physical and chemical properties and are potentially important for various device applications. Here we report the electronic transport and device properties of monolayer molybdenum disulphide grown by chemical vapour deposition. We show that these devices have the potential to suppress short channel effects and have high critical breakdown electric field. However, our study reveals that the electronic properties of these devices are at present severely limited by the presence of a significant amount of band tail trapping states. Through capacitance and ac conductance measurements, we systematically quantify the density-of-states and response time of these states. Because of the large amount of trapped charges, the measured effective mobility also leads to a large underestimation of the true band mobility and the potential of the material. Continual engineering efforts on improving the sample quality are needed for its potential applications.
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                Author and article information

                Journal
                ACS Nanosci Au
                ACS Nanosci Au
                ng
                anaccx
                ACS Nanoscience Au
                American Chemical Society
                2694-2496
                20 October 2023
                20 December 2023
                : 3
                : 6
                : 482-490
                Affiliations
                []Department of Physics and Astronomy & Nebraska Center for Materials and Nanoscience, University of Nebraska−Lincoln , Lincoln, Nebraska 68588-0299, United States
                Author notes
                Author information
                https://orcid.org/0000-0001-6127-349X
                https://orcid.org/0000-0002-2213-6203
                https://orcid.org/0000-0001-6967-4968
                https://orcid.org/0000-0002-7873-5774
                Article
                10.1021/acsnanoscienceau.3c00032
                10740143
                38144704
                4c00dca1-c439-4216-8fc0-459fea69e367
                © 2023 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
                : 01 July 2023
                : 02 October 2023
                : 30 September 2023
                Funding
                Funded by: Division of Materials Research, doi 10.13039/100000078;
                Award ID: 2118828
                Funded by: Nebraska Center for Energy Sciences Research, University of Nebraska-Lincoln, doi 10.13039/100010509;
                Award ID: NA
                Funded by: University of Nebraska-Lincoln, doi 10.13039/100008114;
                Award ID: NA
                Funded by: Division of Electrical, Communications and Cyber Systems, doi 10.13039/100000148;
                Award ID: 2025298
                Funded by: Office of Integrative Activities, doi 10.13039/100000106;
                Award ID: 2044049
                Categories
                Article
                Custom metadata
                ng3c00032
                ng3c00032

                free-standing pzt membranes,ferroelectric hysteresis,depolarization,domain wall roughness,ferroelectric field effect transistors

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