Meichun Fu, Mei Han, Yuan Zhang, Beining Zheng and Shouhua Feng
{"title":"Enhanced negative permittivity by A-site heterovalent ion doping in La1−x−yCaxKyMnO3 perovskites†","authors":"Meichun Fu, Mei Han, Yuan Zhang, Beining Zheng and Shouhua Feng","doi":"10.1039/D4QI03217A","DOIUrl":null,"url":null,"abstract":"<p >Adjusting the concentration of free carriers is a direct strategy to achieve ideal negative permittivity. Employing chemical methods for atypical ion doping is an effective approach to regulate the concentration of free carriers. Owing to the A-site tunability of perovskite manganese oxides, doping with multi-valent ions becomes particularly favorable. In this study, to realize temperature-stable negative permittivity, mono-phase La<small><sub>1−<em>x</em>−<em>y</em></sub></small>Ca<small><sub><em>x</em></sub></small>K<small><sub><em>y</em></sub></small>MnO<small><sub>3</sub></small> (named LCKMO) perovskite crystals having diverse compositions were prepared using an ultra-high-alkaline hydrothermal method. Heterovalent ion doping (La<small><sup>3+</sup></small>, Ca<small><sup>2+</sup></small>, and K<small><sup>+</sup></small>) at the A site within the perovskite crystal structure occurred with the help of the disproportionation reaction of Mn ions at the B site under extreme hydrothermal conditions. By adjusting the La/Ca ratio, we can vary the doping content of K<small><sup>+</sup></small>. Experimental results demonstrate that as the concentration of K<small><sup>+</sup></small> increases, so does the concentration of Mn oxide states, indicating that the increase in free carriers contributes to enhanced negative permittivity and reduced dielectric loss. This work thus pioneers a novel synthetic pathway for the creation and design of materials having negative permittivity.</p>","PeriodicalId":79,"journal":{"name":"Inorganic Chemistry Frontiers","volume":" 13","pages":" 4334-4344"},"PeriodicalIF":6.4000,"publicationDate":"2025-03-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Inorganic Chemistry Frontiers","FirstCategoryId":"92","ListUrlMain":"https://pubs.rsc.org/en/content/articlelanding/2025/qi/d4qi03217a","RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, INORGANIC & NUCLEAR","Score":null,"Total":0}
引用次数: 0
Abstract
Adjusting the concentration of free carriers is a direct strategy to achieve ideal negative permittivity. Employing chemical methods for atypical ion doping is an effective approach to regulate the concentration of free carriers. Owing to the A-site tunability of perovskite manganese oxides, doping with multi-valent ions becomes particularly favorable. In this study, to realize temperature-stable negative permittivity, mono-phase La1−x−yCaxKyMnO3 (named LCKMO) perovskite crystals having diverse compositions were prepared using an ultra-high-alkaline hydrothermal method. Heterovalent ion doping (La3+, Ca2+, and K+) at the A site within the perovskite crystal structure occurred with the help of the disproportionation reaction of Mn ions at the B site under extreme hydrothermal conditions. By adjusting the La/Ca ratio, we can vary the doping content of K+. Experimental results demonstrate that as the concentration of K+ increases, so does the concentration of Mn oxide states, indicating that the increase in free carriers contributes to enhanced negative permittivity and reduced dielectric loss. This work thus pioneers a novel synthetic pathway for the creation and design of materials having negative permittivity.