Underdamped longitudinal soft modes in ionic crystallites-lattice and charge motions observed by ultrafast x-ray diffraction.

Structural dynamics (Melville, N.Y.) Pub Date : 2022-03-08 eCollection Date: 2022-03-01 DOI:10.1063/4.0000143
Isabel Gonzalez-Vallejo, Azize Koç, Klaus Reimann, Michael Woerner, Thomas Elsaesser
{"title":"Underdamped longitudinal soft modes in ionic crystallites-lattice and charge motions observed by ultrafast x-ray diffraction.","authors":"Isabel Gonzalez-Vallejo,&nbsp;Azize Koç,&nbsp;Klaus Reimann,&nbsp;Michael Woerner,&nbsp;Thomas Elsaesser","doi":"10.1063/4.0000143","DOIUrl":null,"url":null,"abstract":"<p><p>Soft modes in crystals are lattice vibrations with frequencies that decrease and eventually vanish as the temperature approaches a critical point, e.g., a structural change due to a phase transition. In ionic para- or ferroelectric materials, the frequency decrease is connected with a diverging electric susceptibility and, for infrared active modes, a strong increase in oscillator strength. The traditional picture describes soft modes as overdamped transverse optical phonons of a hybrid vibrational-electronic character. In this context, potassium dihydrogen phosphate (KH<sub>2</sub>PO<sub>4</sub>, KDP) has been studied for decades as a prototypical material with, however, inconclusive results regarding the soft modes in its para- and ferroelectric phase. There are conflicting assignments of soft-mode frequencies and damping parameters. We report the first observation of a longitudinal underdamped soft mode in paraelectric KDP. Upon impulsive femtosecond Raman excitation of coherent low-frequency phonons in the electronic ground state of KDP crystallites, transient powder diffraction patterns are recorded with femtosecond hard x-ray pulses. Electron density maps derived from the x-ray data reveal oscillatory charge relocations over interatomic distances, much larger than the sub-picometer nuclear displacements, a direct hallmark of soft-mode behavior. The strongly underdamped character of the soft mode manifests in charge oscillations persisting for more than 10 ps. The soft-mode frequency decreases from 0.55 THz at <i>T </i>=<i> </i>295 K to 0.39 THz at <i>T </i>=<i> </i>175 K. An analysis of the Raman excitation conditions in crystallites and the weak damping demonstrate a longitudinal character. Our results extend soft-mode physics well beyond the traditional picture and pave the way for an atomic-level characterization of soft modes.</p>","PeriodicalId":520783,"journal":{"name":"Structural dynamics (Melville, N.Y.)","volume":" ","pages":"024501"},"PeriodicalIF":0.0000,"publicationDate":"2022-03-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8906907/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Structural dynamics (Melville, N.Y.)","FirstCategoryId":"101","ListUrlMain":"https://doi.org/10.1063/4.0000143","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2022/3/1 0:00:00","PubModel":"eCollection","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

Soft modes in crystals are lattice vibrations with frequencies that decrease and eventually vanish as the temperature approaches a critical point, e.g., a structural change due to a phase transition. In ionic para- or ferroelectric materials, the frequency decrease is connected with a diverging electric susceptibility and, for infrared active modes, a strong increase in oscillator strength. The traditional picture describes soft modes as overdamped transverse optical phonons of a hybrid vibrational-electronic character. In this context, potassium dihydrogen phosphate (KH2PO4, KDP) has been studied for decades as a prototypical material with, however, inconclusive results regarding the soft modes in its para- and ferroelectric phase. There are conflicting assignments of soft-mode frequencies and damping parameters. We report the first observation of a longitudinal underdamped soft mode in paraelectric KDP. Upon impulsive femtosecond Raman excitation of coherent low-frequency phonons in the electronic ground state of KDP crystallites, transient powder diffraction patterns are recorded with femtosecond hard x-ray pulses. Electron density maps derived from the x-ray data reveal oscillatory charge relocations over interatomic distances, much larger than the sub-picometer nuclear displacements, a direct hallmark of soft-mode behavior. The strongly underdamped character of the soft mode manifests in charge oscillations persisting for more than 10 ps. The soft-mode frequency decreases from 0.55 THz at T =295 K to 0.39 THz at T =175 K. An analysis of the Raman excitation conditions in crystallites and the weak damping demonstrate a longitudinal character. Our results extend soft-mode physics well beyond the traditional picture and pave the way for an atomic-level characterization of soft modes.

Abstract Image

Abstract Image

Abstract Image

离子晶体的欠阻尼纵向软模式——超快x射线衍射观察到的晶格和电荷运动。
晶体中的软模式是晶格振动,其频率随着温度接近临界点而降低并最终消失,例如,由于相变引起的结构变化。在离子对电或铁电材料中,频率的降低与电磁化率的发散有关,而对于红外主动模式,则与振荡器强度的强烈增加有关。传统图像将软模描述为振动电子混合特性的过阻尼横向光学声子。在这种情况下,磷酸二氢钾(KH2PO4, KDP)作为一种原型材料已经被研究了几十年,然而,关于其对电相和铁电相的软模式,没有确定的结果。软模频率和阻尼参数的分配存在冲突。我们报告了在准电KDP中首次观察到的纵向欠阻尼软模式。在KDP晶体电子基态的相干低频声子的飞秒拉曼脉冲激发下,用飞秒硬x射线脉冲记录了瞬态粉末衍射图样。来自x射线数据的电子密度图揭示了振荡电荷在原子间距离上的重定位,远大于亚皮米核位移,这是软模式行为的直接标志。软模的弱阻尼特性表现为持续10 ps以上的电荷振荡,软模频率从T = 295 K时的0.55 THz下降到T = 175 K时的0.39 THz。对微晶中的拉曼激发条件和弱阻尼的分析表明其具有纵向特征。我们的研究结果将软模式物理扩展到传统图像之外,并为软模式的原子级表征铺平了道路。
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 求助全文
来源期刊
自引率
0.00%
发文量
0
×
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
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
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 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信