Ultrahigh Negative Longitudinal Piezoelectricity in Rhombohedral GeTe and Its Group IV-VI Analogues.

IF 9.1 1区 材料科学 Q1 CHEMISTRY, MULTIDISCIPLINARY Nano Letters Pub Date : 2025-03-05 Epub Date: 2025-02-20 DOI:10.1021/acs.nanolett.4c06671
Yang Liu, Wei Wang, Zhengjie Wang, Chen Si
{"title":"Ultrahigh Negative Longitudinal Piezoelectricity in Rhombohedral GeTe and Its Group IV-VI Analogues.","authors":"Yang Liu, Wei Wang, Zhengjie Wang, Chen Si","doi":"10.1021/acs.nanolett.4c06671","DOIUrl":null,"url":null,"abstract":"<p><p>Conventional piezoelectric materials typically exhibit positive longitudinal piezoelectric coefficients, yet recent studies have identified exceptions with negative piezoelectric responses. Using density functional theory, we demonstrate for the first time that rhombohedral GeTe (r-GeTe) possesses an ultrahigh negative piezoelectric strain coefficient (<i>d</i><sub>33</sub>) of -70.87 pC/N, surpassing all previously reported negative piezoelectric materials. This phenomenon arises from the \"quasi-layered\" structure of r-GeTe, comprising alternating strong and weak bonds, which induces a pronounced negative internal-strain contribution and an exceptionally low elastic constant. We further extend our investigation to other IV-VI rhombohedral materials, identifying GeS, GeSe, and SiTe as promising candidates for ultrahigh negative piezoelectricity. In contrast to prior reports, where negative piezoelectricity stems from a negative clamped-ion term that dominates a small positive internal-strain contribution, our findings propose a new material design strategy for large negative piezoelectricity by introducing a significantly negative internal strain, along with the negative clamped-ion term.</p>","PeriodicalId":53,"journal":{"name":"Nano Letters","volume":" ","pages":"3630-3636"},"PeriodicalIF":9.1000,"publicationDate":"2025-03-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Nano Letters","FirstCategoryId":"88","ListUrlMain":"https://doi.org/10.1021/acs.nanolett.4c06671","RegionNum":1,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/2/20 0:00:00","PubModel":"Epub","JCR":"Q1","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0

Abstract

Conventional piezoelectric materials typically exhibit positive longitudinal piezoelectric coefficients, yet recent studies have identified exceptions with negative piezoelectric responses. Using density functional theory, we demonstrate for the first time that rhombohedral GeTe (r-GeTe) possesses an ultrahigh negative piezoelectric strain coefficient (d33) of -70.87 pC/N, surpassing all previously reported negative piezoelectric materials. This phenomenon arises from the "quasi-layered" structure of r-GeTe, comprising alternating strong and weak bonds, which induces a pronounced negative internal-strain contribution and an exceptionally low elastic constant. We further extend our investigation to other IV-VI rhombohedral materials, identifying GeS, GeSe, and SiTe as promising candidates for ultrahigh negative piezoelectricity. In contrast to prior reports, where negative piezoelectricity stems from a negative clamped-ion term that dominates a small positive internal-strain contribution, our findings propose a new material design strategy for large negative piezoelectricity by introducing a significantly negative internal strain, along with the negative clamped-ion term.

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
菱形GeTe及其IV-VI族类似物的超高负纵向压电性。
传统的压电材料通常表现为正的纵向压电系数,但最近的研究发现了负压电响应的例外。利用密度泛函理论,我们首次证明了菱形GeTe (r-GeTe)具有超高的负压电应变系数(d33),为-70.87 pC/N,超过了之前报道的所有负压电材料。这种现象是由r-GeTe的“准层状”结构引起的,该结构由强弱键交替组成,导致明显的负内应变贡献和极低的弹性常数。我们进一步将我们的研究扩展到其他IV-VI菱形材料,确定GeS, GeSe和SiTe作为超高负压电性的有前途的候选者。与之前的报道相反,负压电源于负箝位离子项,该负箝位离子项主导了小的正内应变贡献,我们的研究结果提出了一种新的材料设计策略,通过引入显着的负内应变,以及负箝位离子项来实现大的负压电性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
Nano Letters
Nano Letters 工程技术-材料科学:综合
CiteScore
16.80
自引率
2.80%
发文量
1182
审稿时长
1.4 months
期刊介绍: Nano Letters serves as a dynamic platform for promptly disseminating original results in fundamental, applied, and emerging research across all facets of nanoscience and nanotechnology. A pivotal criterion for inclusion within Nano Letters is the convergence of at least two different areas or disciplines, ensuring a rich interdisciplinary scope. The journal is dedicated to fostering exploration in diverse areas, including: - Experimental and theoretical findings on physical, chemical, and biological phenomena at the nanoscale - Synthesis, characterization, and processing of organic, inorganic, polymer, and hybrid nanomaterials through physical, chemical, and biological methodologies - Modeling and simulation of synthetic, assembly, and interaction processes - Realization of integrated nanostructures and nano-engineered devices exhibiting advanced performance - Applications of nanoscale materials in living and environmental systems Nano Letters is committed to advancing and showcasing groundbreaking research that intersects various domains, fostering innovation and collaboration in the ever-evolving field of nanoscience and nanotechnology.
期刊最新文献
Entropy Engineering-Driven Solid Solution of Metal Carbide Nanoparticles for Electrocatalytic Hydrogen Evolution Reaction. Reprogramming Chirality in Peptide Self-Assembly via Intramolecular Side Chain-Backbone Hydrogen Bonding. Quantum Sensing of Opaque Materials with Plasmonically Enhanced Hexagonal Boron Nitride Spin Defects. Dual-Interface Hierarchical Assembly of Asymmetric ICG-Lipid Conjugates Enables Finite J-type Aggregation and Two-Stage NIR-II Fluorescence Enhancement. Observation of Spin–Orbit Coupled Polariton Vortices at Room Temperature
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1