Revealing the Origin of Property Discrepancy in KNN‐Based Ceramics with Extreme K/Na Ratio for Sensing Application

IF 13 2区 材料科学 Q1 CHEMISTRY, MULTIDISCIPLINARY
Small Pub Date : 2025-04-24 DOI:10.1002/smll.202502418
Yi Ding, Zhi Tan, Yongqi Pan, Yu Wang, Yangda Dong, Wenbin Liu, Ting Zheng, Jiagang Wu
{"title":"Revealing the Origin of Property Discrepancy in KNN‐Based Ceramics with Extreme K/Na Ratio for Sensing Application","authors":"Yi Ding, Zhi Tan, Yongqi Pan, Yu Wang, Yangda Dong, Wenbin Liu, Ting Zheng, Jiagang Wu","doi":"10.1002/smll.202502418","DOIUrl":null,"url":null,"abstract":"Potassium–sodium niobate (KNN) ceramics are critical lead‐free piezoelectric materials, offering eco‐friendly alternatives with high performance for sustainable sensor applications. However, how to overcome the theoretical framework of conventional K/Na ratio limitation and achieve property enhancement in extreme composition remains to be fully understood. Herein, by combining density function theory calculation, Rayleigh analysis, and ferroelectric scaling behavior, the origin of property discrepancy in KNN‐based ceramics with extreme K/Na ratio is unveiled. Compared with Na‐rich sample, 2.3‐fold enhanced piezoelectricity can be achieved in K‐rich ceramics, superior to those with similar high K concentration. The deteriorated property in Na‐rich sample comes from the existence of in‐phase oxygen octahedron tilting (M<jats:sub>2</jats:sub><jats:sup>+</jats:sup>) mode, suppressing the polar () mode and leading to a higher energy barrier. Nevertheless, the absence of M<jats:sub>2</jats:sub><jats:sup>+</jats:sup> mode and the multiphase coexistence with a maze‐like domain, promote polarization rotation and domain switching, resulting in improved piezoelectric response in K‐rich ceramics. A compression‐type accelerometer based on KNN with extreme K/Na ratio is designed and the sensitivity of K‐rich ceramics is also much higher than that of Na‐rich ones, highest in reported KNN‐based piezoelectric accelerometers. The study provides a new paradigm to boost electrical properties and reveals the underlying mechanism of property discrepancy induced by extreme K/Na ratio, beneficial to the development of sensor applications.","PeriodicalId":228,"journal":{"name":"Small","volume":"35 1","pages":""},"PeriodicalIF":13.0000,"publicationDate":"2025-04-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Small","FirstCategoryId":"88","ListUrlMain":"https://doi.org/10.1002/smll.202502418","RegionNum":2,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0

Abstract

Potassium–sodium niobate (KNN) ceramics are critical lead‐free piezoelectric materials, offering eco‐friendly alternatives with high performance for sustainable sensor applications. However, how to overcome the theoretical framework of conventional K/Na ratio limitation and achieve property enhancement in extreme composition remains to be fully understood. Herein, by combining density function theory calculation, Rayleigh analysis, and ferroelectric scaling behavior, the origin of property discrepancy in KNN‐based ceramics with extreme K/Na ratio is unveiled. Compared with Na‐rich sample, 2.3‐fold enhanced piezoelectricity can be achieved in K‐rich ceramics, superior to those with similar high K concentration. The deteriorated property in Na‐rich sample comes from the existence of in‐phase oxygen octahedron tilting (M2+) mode, suppressing the polar () mode and leading to a higher energy barrier. Nevertheless, the absence of M2+ mode and the multiphase coexistence with a maze‐like domain, promote polarization rotation and domain switching, resulting in improved piezoelectric response in K‐rich ceramics. A compression‐type accelerometer based on KNN with extreme K/Na ratio is designed and the sensitivity of K‐rich ceramics is also much higher than that of Na‐rich ones, highest in reported KNN‐based piezoelectric accelerometers. The study provides a new paradigm to boost electrical properties and reveals the underlying mechanism of property discrepancy induced by extreme K/Na ratio, beneficial to the development of sensor applications.
揭示极端K/Na比KNN基陶瓷在传感应用中性能差异的来源
铌酸钾钠(KNN)陶瓷是一种重要的无铅压电材料,为可持续传感器应用提供了高性能的环保替代品。然而,如何克服传统K/Na比限制的理论框架,并在极端成分下实现性能增强,仍有待于充分理解。本文结合密度泛函理论计算、瑞利分析和铁电结垢行为,揭示了极端K/Na比下KNN基陶瓷性能差异的原因。与富钠样品相比,富钾陶瓷的压电性提高了2.3倍,优于同样高钾浓度的陶瓷。富钠样品的性能恶化是由于相氧八面体倾斜(M2+)模式的存在,抑制了极性()模式,导致了更高的能垒。然而,M2+模式的缺失和迷宫状畴的多相共存促进了极化旋转和畴切换,从而改善了富K陶瓷的压电响应。设计了一种基于KNN的压缩型加速度计,具有极高的K/Na比,富K陶瓷的灵敏度也远高于富Na陶瓷,是目前报道的基于KNN的压电加速度计中最高的。该研究提供了一种提高电性能的新范式,揭示了极端K/Na比导致电性能差异的潜在机制,有利于传感器应用的发展。
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
Small
Small 工程技术-材料科学:综合
CiteScore
17.70
自引率
3.80%
发文量
1830
审稿时长
2.1 months
期刊介绍: Small serves as an exceptional platform for both experimental and theoretical studies in fundamental and applied interdisciplinary research at the nano- and microscale. The journal offers a compelling mix of peer-reviewed Research Articles, Reviews, Perspectives, and Comments. With a remarkable 2022 Journal Impact Factor of 13.3 (Journal Citation Reports from Clarivate Analytics, 2023), Small remains among the top multidisciplinary journals, covering a wide range of topics at the interface of materials science, chemistry, physics, engineering, medicine, and biology. Small's readership includes biochemists, biologists, biomedical scientists, chemists, engineers, information technologists, materials scientists, physicists, and theoreticians alike.
×
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