High-entropy assisted capacitive energy storage in relaxor ferroelectrics by chemical short-range order

Abstract Next-generation advanced high/pulsed power capacitors rely heavily on dielectric ceramics with high energy storage performance. Although high entropy relaxor ferroelectric exhibited enormous potential in functional materials, the chemical short-range order, which is a common phenomenon in h...

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Main Authors: Tongxin Wei, Jinzhu Zou, Xuefan Zhou, Miao Song, Yan Zhang, Cewen Nan, Yuanhua Lin, Dou Zhang
Format: Article
Language:English
Published: Nature Portfolio 2025-01-01
Series:Nature Communications
Online Access:https://doi.org/10.1038/s41467-025-56181-6
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author Tongxin Wei
Jinzhu Zou
Xuefan Zhou
Miao Song
Yan Zhang
Cewen Nan
Yuanhua Lin
Dou Zhang
author_facet Tongxin Wei
Jinzhu Zou
Xuefan Zhou
Miao Song
Yan Zhang
Cewen Nan
Yuanhua Lin
Dou Zhang
author_sort Tongxin Wei
collection DOAJ
description Abstract Next-generation advanced high/pulsed power capacitors rely heavily on dielectric ceramics with high energy storage performance. Although high entropy relaxor ferroelectric exhibited enormous potential in functional materials, the chemical short-range order, which is a common phenomenon in high entropy alloys to modulate performances, have been paid less attention here. We design a chemical short-range order strategy to modulate polarization response under external electric field and achieve substantial enhancements of energy storage properties, i.e. an ultrahigh energy density of ~16.4 J/cm3 with markedly improved efficiency ~90% at an electric field of 85 kV/mm in Nb doped (Bi0.2Na0.2K0.2La0.2Sr0.2) TiO3 system. Atomic-scale scanning transmission electron microscopy observations show that Nb exhibits a chemical short-range order structure, with Nb enriched regions displaying ultrasmall polar nanoregions and more flexible polarization configurations, which is conducive to achieving high maximum polarization and low residual polarization. Moreover, refined grain size of ~0.25μm, suppressed oxygen vacancies and enhanced bandwidth contribute to a high breakdown field strength. These collective factors result in exceptionally high energy storage density and efficiency. This short-range order strategy is expected to enhance the functional performances in other high entropy relaxor ferroelectrics.
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issn 2041-1723
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publishDate 2025-01-01
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spelling doaj-art-1430b94c150a4481a0d241e37e97dd6d2025-01-19T12:31:08ZengNature PortfolioNature Communications2041-17232025-01-0116111110.1038/s41467-025-56181-6High-entropy assisted capacitive energy storage in relaxor ferroelectrics by chemical short-range orderTongxin Wei0Jinzhu Zou1Xuefan Zhou2Miao Song3Yan Zhang4Cewen Nan5Yuanhua Lin6Dou Zhang7State Key Laboratory of Powder Metallurgy, Central South UniversityState Key Laboratory of Powder Metallurgy, Central South UniversityState Key Laboratory of Powder Metallurgy, Central South UniversityState Key Laboratory of Powder Metallurgy, Central South UniversityState Key Laboratory of Powder Metallurgy, Central South UniversityState Key Laboratory of New Ceramics and Fine Processing, School of Materials Science and Engineering, Tsinghua UniversityState Key Laboratory of New Ceramics and Fine Processing, School of Materials Science and Engineering, Tsinghua UniversityState Key Laboratory of Powder Metallurgy, Central South UniversityAbstract Next-generation advanced high/pulsed power capacitors rely heavily on dielectric ceramics with high energy storage performance. Although high entropy relaxor ferroelectric exhibited enormous potential in functional materials, the chemical short-range order, which is a common phenomenon in high entropy alloys to modulate performances, have been paid less attention here. We design a chemical short-range order strategy to modulate polarization response under external electric field and achieve substantial enhancements of energy storage properties, i.e. an ultrahigh energy density of ~16.4 J/cm3 with markedly improved efficiency ~90% at an electric field of 85 kV/mm in Nb doped (Bi0.2Na0.2K0.2La0.2Sr0.2) TiO3 system. Atomic-scale scanning transmission electron microscopy observations show that Nb exhibits a chemical short-range order structure, with Nb enriched regions displaying ultrasmall polar nanoregions and more flexible polarization configurations, which is conducive to achieving high maximum polarization and low residual polarization. Moreover, refined grain size of ~0.25μm, suppressed oxygen vacancies and enhanced bandwidth contribute to a high breakdown field strength. These collective factors result in exceptionally high energy storage density and efficiency. This short-range order strategy is expected to enhance the functional performances in other high entropy relaxor ferroelectrics.https://doi.org/10.1038/s41467-025-56181-6
spellingShingle Tongxin Wei
Jinzhu Zou
Xuefan Zhou
Miao Song
Yan Zhang
Cewen Nan
Yuanhua Lin
Dou Zhang
High-entropy assisted capacitive energy storage in relaxor ferroelectrics by chemical short-range order
Nature Communications
title High-entropy assisted capacitive energy storage in relaxor ferroelectrics by chemical short-range order
title_full High-entropy assisted capacitive energy storage in relaxor ferroelectrics by chemical short-range order
title_fullStr High-entropy assisted capacitive energy storage in relaxor ferroelectrics by chemical short-range order
title_full_unstemmed High-entropy assisted capacitive energy storage in relaxor ferroelectrics by chemical short-range order
title_short High-entropy assisted capacitive energy storage in relaxor ferroelectrics by chemical short-range order
title_sort high entropy assisted capacitive energy storage in relaxor ferroelectrics by chemical short range order
url https://doi.org/10.1038/s41467-025-56181-6
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