{"title":"Giant Dielectric Permittivity and Electronic Structure in Hydrogenated (La/Mn) Merge Codoped TiO2 Ceramics","authors":"A. A. Dakhel","doi":"10.1007/s13538-024-01582-z","DOIUrl":null,"url":null,"abstract":"<div><p>Titanium oxide (TiO<sub>2</sub>) nanoparticles (NPs) codoped with (La/Mn) ions were synthesized by a hydrothermal decomposition technique. The prepared codoped NPs were hydrogenated at 400 °C and systematically studied by X‐ray diffraction (XRD), optical diffuse reflection spectroscopy (DRS), and electrical insulating measurements. The codoped solid solution (SS) NPs were prepared to be built of core/shell-like electronic nanostructures that having giant permittivity (GP) of order 10<sup>4</sup>, which is extremely higher than that of undoped TiO<sub>2</sub>. The electronic nature of the built structures was described according to the foundation of the doping mechanisms. Thus, the codoping was employed in the present work to fabricate coalesce dielectric crystalline medium of GP. Two Mn-dopant concentrations were used in the present investigation for comparison. Thus, the objective of creation of GP properties was successfully achieved. Moreover, the results of the electrical measurements were analyzed according to the available models: the correlated barrier hopping (CBH) model, the polarons-hopping conduction model, and Jonsher’s AC power law.</p></div>","PeriodicalId":499,"journal":{"name":"Brazilian Journal of Physics","volume":"54 6","pages":""},"PeriodicalIF":1.5000,"publicationDate":"2024-08-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Brazilian Journal of Physics","FirstCategoryId":"101","ListUrlMain":"https://link.springer.com/article/10.1007/s13538-024-01582-z","RegionNum":4,"RegionCategory":"物理与天体物理","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"PHYSICS, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0
Abstract
Titanium oxide (TiO2) nanoparticles (NPs) codoped with (La/Mn) ions were synthesized by a hydrothermal decomposition technique. The prepared codoped NPs were hydrogenated at 400 °C and systematically studied by X‐ray diffraction (XRD), optical diffuse reflection spectroscopy (DRS), and electrical insulating measurements. The codoped solid solution (SS) NPs were prepared to be built of core/shell-like electronic nanostructures that having giant permittivity (GP) of order 104, which is extremely higher than that of undoped TiO2. The electronic nature of the built structures was described according to the foundation of the doping mechanisms. Thus, the codoping was employed in the present work to fabricate coalesce dielectric crystalline medium of GP. Two Mn-dopant concentrations were used in the present investigation for comparison. Thus, the objective of creation of GP properties was successfully achieved. Moreover, the results of the electrical measurements were analyzed according to the available models: the correlated barrier hopping (CBH) model, the polarons-hopping conduction model, and Jonsher’s AC power law.
通过水热分解技术合成了掺杂(La/Mn)离子的氧化钛(TiO2)纳米粒子(NPs)。制备的掺杂 NPs 在 400 °C 下氢化,并通过 X 射线衍射 (XRD)、光学漫反射光谱 (DRS) 和电绝缘测量进行了系统研究。制备出的掺杂固溶体(SS)纳米粒子由核/壳状电子纳米结构组成,其巨导率(GP)为 104,远高于未掺杂的二氧化钛。根据掺杂机制的基础,对所构建结构的电子性质进行了描述。因此,本研究采用了共掺杂的方法来制造具有 GP 的凝聚介电晶体介质。本研究中使用了两种锰掺杂浓度进行比较。因此,成功实现了创造 GP 特性的目标。此外,电学测量结果根据现有模型进行了分析:相关势垒跳变(CBH)模型、极子跳变传导模型和 Jonsher 交流幂律。
期刊介绍:
The Brazilian Journal of Physics is a peer-reviewed international journal published by the Brazilian Physical Society (SBF). The journal publishes new and original research results from all areas of physics, obtained in Brazil and from anywhere else in the world. Contents include theoretical, practical and experimental papers as well as high-quality review papers. Submissions should follow the generally accepted structure for journal articles with basic elements: title, abstract, introduction, results, conclusions, and references.