High entropy induced superior weakly coupled relaxor phase and suppression interfacial polarization in (Bi0.3Na0.3Sr0.3Ba0.1)(Ti1-xNbx)O3 ceramics

IF 4.7 3区 材料科学 Q2 MATERIALS SCIENCE, MULTIDISCIPLINARY Materials Chemistry and Physics Pub Date : 2025-04-01 Epub Date: 2025-01-23 DOI:10.1016/j.matchemphys.2025.130446
Kamal A. Aly , Yasser A.M. Ismail , Abdullah Saad Alsubaie , Abd El-razek Mahmoud
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Abstract

Dielectric ceramics with high configurational entropy (ΔS) and superior thermal stability in dielectric properties are tremendous promise materials for high performance of energy storage. However, interfacial polarization is the major challenge for superior energy storage performance. Herein, high-entropy and grain resistance strategy disrupts ferroelectricity long-range ordering in (Na0.5Bi0.5)TiO3 ceramics via A/B-sites cation disorder. Lead free ceramics of (Bi0.3Na0.3Sr0.3Ba0.1)(Ti1-xNbx)O3 (x = 0.0, 0.025, 0.05, 0.075 and 0.1) (abbreviate BBSNTNbx) were prepared using solid solution technique. The obtained results reveal that ΔS increased from 1.31R for x = 0.0–1.64R for x = 0.1 resulting in superior weakly coupled relaxor phase of BO6. The imbalance of ion valances between donor Nb5+ and Ti4+ may force Ti4+ to become Ti3+ resulting in formation of Nb5+-Ti3+ ion pair leading to negligible remnant polarization (Pr). High entropy induced elevation the grain resistance and suppression interfacial polarization. As entropy increases from 1.31R to 1.64R, the energy storage efficiency (ƞ) increased from ∼83 % to 98 %. Furthermore, superior temperature stability across a broad temperature range 25–175 °C in both of Wrec and ƞ were investigated at high entropy. This research presents an effective method for designing NBT - based ceramics with suppression of interfacial polarization and ultra-high comprehensive energy storage performance.
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在(Bi0.3Na0.3Sr0.3Ba0.1)(Ti1-xNbx)O3陶瓷中,高熵诱导出优异的弱耦合弛豫相和抑制界面极化
介电陶瓷具有高构型熵(ΔS)和优越的介电性能热稳定性,是极有前途的高性能储能材料。然而,界面极化是实现优异储能性能的主要挑战。本文中,高熵和晶粒电阻策略通过A/ b位阳离子无序破坏(Na0.5Bi0.5)TiO3陶瓷的铁电性长程有序。采用固溶体法制备了(Bi0.3Na0.3Sr0.3Ba0.1)(Ti1-xNbx)O3 (x = 0.0, 0.025, 0.05, 0.075和0.1)(简称BBSNTNbx)无铅陶瓷。结果表明,当x = 0.0时,ΔS从1.31R增加到1.64 r,导致BO6弱耦合弛豫相优越。供体Nb5+和Ti4+之间离子价的不平衡可能迫使Ti4+变成Ti3+,从而形成Nb5+-Ti3+离子对,导致可忽略的残余极化(Pr)。高熵诱导晶粒阻力升高,抑制界面极化。当熵从1.31R增加到1.64R时,能量存储效率(±)从83%增加到98%。此外,在高熵条件下,研究了wrc和l在25-175°C的宽温度范围内的优越温度稳定性。本研究提出了一种有效的方法来设计具有抑制界面极化和超高综合储能性能的NBT基陶瓷。
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来源期刊
Materials Chemistry and Physics
Materials Chemistry and Physics 工程技术-材料科学:综合
CiteScore
8.70
自引率
4.30%
发文量
1515
审稿时长
69 days
期刊介绍: Materials Chemistry and Physics is devoted to short communications, full-length research papers and feature articles on interrelationships among structure, properties, processing and performance of materials. The Editors welcome manuscripts on thin films, surface and interface science, materials degradation and reliability, metallurgy, semiconductors and optoelectronic materials, fine ceramics, magnetics, superconductors, specialty polymers, nano-materials and composite materials.
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