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应变四方二氧化铈中增强的非经典电致伸缩效应

Enhanced non-classical electrostriction in strained tetragonal ceria.

作者信息

Santucci Simone, Vasiljevic Milica, Zhang Haiwu, Tinti Victor Buratto, Bergne Achilles, Morin-Martinez Armando A, Chaluvadi Sandeep Kumar, Orgiani Pasquale, Sanna Simone, Lyksborg-Andersen Anton, Hansen Thomas Willum, Castelli Ivano E, Pryds Nini, Esposito Vincenzo

机构信息

Department of Energy Conversion and Storage, Technical University of Denmark, Lyngby, Denmark.

Atlant 3D, Taastrup, Denmark.

出版信息

Nat Commun. 2025 Jan 2;16(1):36. doi: 10.1038/s41467-024-55393-6.

DOI:10.1038/s41467-024-55393-6
PMID:39747024
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11697435/
Abstract

Electrostriction is the upsurge of strain under an electric field in any dielectric material. Oxygen-defective metal oxides, such as acceptor-doped ceria, exhibit high electrostriction 10 mV values, which can be further enhanced via interface engineering at the nanoscale. This effect in ceria is "non-classical" as it arises from an intricate relation between defect-induced polarisation and local elastic distortion in the lattice. Here, we investigate the impact of mismatch strain when epitaxial Gd-doped CeO thin films are grown on various single-crystal substrates. We demonstrate that varying the compressive and tensile strain can fine-tune the electromechanical response. The electrostriction coefficients achieve a large M ≈ 3.6·10 mV in lattices of in-plane compressed films, i.e., a positive tetragonality (c/a-1 > 0), with stress above 3 GPa at the film/substrate interface. Chemical and structural analysis suggests that the high electrostriction stems from anisotropic distortions in the local lattice strain, which lead to constructively oriented elastic dipoles and Ce electronic defects.

摘要

电致伸缩是指任何介电材料在电场作用下应变的激增。缺氧金属氧化物,如受主掺杂的二氧化铈,表现出高电致伸缩值(10 mV),通过纳米尺度的界面工程可进一步提高该值。二氧化铈中的这种效应是“非经典的”,因为它源于缺陷诱导极化与晶格中局部弹性畸变之间的复杂关系。在此,我们研究了在各种单晶衬底上生长外延钆掺杂二氧化铈薄膜时失配应变的影响。我们证明,改变压缩应变和拉伸应变可以微调机电响应。在面内压缩薄膜的晶格中,即正四方性(c/a - 1 > 0),当薄膜/衬底界面处的应力高于3 GPa时,电致伸缩系数达到较大的M ≈ 3.6·10 mV。化学和结构分析表明,高电致伸缩源于局部晶格应变中的各向异性畸变,这导致了建设性取向的弹性偶极子和铈电子缺陷。

相似文献

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Enhanced non-classical electrostriction in strained tetragonal ceria.应变四方二氧化铈中增强的非经典电致伸缩效应
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本文引用的文献

1
Tunable Ferroionic Properties in CeO/BaTiO Heterostructures.CeO/BaTiO异质结构中的可调铁离子特性
ACS Appl Mater Interfaces. 2024 Sep 25;16(38):50679-50689. doi: 10.1021/acsami.4c09477. Epub 2024 Sep 13.
2
Oxygen-defective electrostrictors for soft electromechanics.用于软机电的缺氧电致伸缩器。
Sci Adv. 2024 Aug 30;10(35):eadq3444. doi: 10.1126/sciadv.adq3444.
3
Lead-free Zr-doped ceria ceramics with low permittivity displaying giant electrostriction.具有低介电常数并表现出巨大电致伸缩效应的无铅锆掺杂氧化铈陶瓷。
Nat Commun. 2023 Nov 15;14(1):7371. doi: 10.1038/s41467-023-43032-5.
4
Atomically engineered interfaces yield extraordinary electrostriction.原子工程界面产生非凡的电致伸缩效应。
Nature. 2022 Sep;609(7928):695-700. doi: 10.1038/s41586-022-05073-6. Epub 2022 Sep 21.
5
Induced giant piezoelectricity in centrosymmetric oxides.诱导中心对称氧化物产生巨大压电性。
Science. 2022 Feb 11;375(6581):653-657. doi: 10.1126/science.abm7497. Epub 2022 Feb 10.
6
Electromechanically active pair dynamics in a Gd-doped ceria single crystal.钆掺杂二氧化铈单晶中的机电活性对动力学
Phys Chem Chem Phys. 2021 May 19;23(19):11233-11239. doi: 10.1039/d1cp00748c.
7
Anisotropic Strain in Rare-Earth Substituted Ceria Thin Films Probed by Polarized Raman Spectroscopy and First-Principles Calculations.通过偏振拉曼光谱和第一性原理计算探测稀土取代二氧化铈薄膜中的各向异性应变
ACS Appl Mater Interfaces. 2020 Dec 16;12(50):56251-56259. doi: 10.1021/acsami.0c14249. Epub 2020 Dec 3.
8
Improved Structural Properties in Homogeneously Doped SmCeO Epitaxial Thin Films: High Doping Effect on the Electronic Bands.均匀掺杂的SmCeO外延薄膜中结构性能的改善:高掺杂对电子能带的影响
ACS Appl Mater Interfaces. 2020 Oct 21;12(42):47556-47563. doi: 10.1021/acsami.0c13495. Epub 2020 Oct 8.
9
Atomic-scale insights into electro-steric substitutional chemistry of cerium oxide.氧化铈电子空间取代化学的原子尺度洞察。
Phys Chem Chem Phys. 2020 Oct 7;22(38):21900-21908. doi: 10.1039/d0cp03298k.
10
A review of defect structure and chemistry in ceria and its solid solutions.氧化铈及其固溶体的缺陷结构和化学综述。
Chem Soc Rev. 2020 Jan 21;49(2):554-592. doi: 10.1039/c9cs00588a. Epub 2019 Dec 24.