Enhanced negative permittivity by A-site heterovalent ion doping in La1−x−yCaxKyMnO3 perovskites†

IF 6.4 1区 化学 Q1 CHEMISTRY, INORGANIC & NUCLEAR
Meichun Fu, Mei Han, Yuan Zhang, Beining Zheng and Shouhua Feng
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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−xyCaxKyMnO3 (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.

Abstract Image

La1-x-yCaxKyMnO3钙钛矿a位杂价离子掺杂增强负介电常数
调节自由载流子的浓度是获得理想负介电常数的直接策略。采用化学方法进行非典型离子掺杂是调控自由载流子浓度的有效途径。由于钙钛矿锰氧化物的a位可调性,多价离子掺杂变得特别有利。为了实现温度稳定的负介电常数,本研究采用超高碱性水热法制备了不同组成的单相La1-x-yCaxKyMnO3 (LCKMO)钙钛矿晶体。在极端水热条件下,钙钛矿晶体结构中a位的异价离子掺杂(La3+, Ca2+, K+)是借助b位Mn离子的歧化反应发生的。通过调整La/Ca比值,可以改变K+的掺杂含量。实验结果表明,随着K+浓度的增加,Mn氧化物态的浓度也随之增加,这表明额外的自由载流子的存在导致了更负的介电常数和最小的介电损耗。这项工作为负介电常数材料的创造和设计开辟了一条新的合成途径。
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来源期刊
Inorganic Chemistry Frontiers
Inorganic Chemistry Frontiers CHEMISTRY, INORGANIC & NUCLEAR-
CiteScore
10.40
自引率
7.10%
发文量
587
审稿时长
1.2 months
期刊介绍: The international, high quality journal for interdisciplinary research between inorganic chemistry and related subjects
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