Herbert Kobald, Alexander M Kobald, Ivana Panzic, Marco Deluca
{"title":"Enhanced energy storage in relaxor (1-x)Bi<sub>0.5</sub>Na<sub>0.5</sub>TiO<sub>3</sub>-xBaZr<sub>y</sub>Ti<sub>1-y</sub>O<sub>3</sub> thin films by morphotropic phase boundary engineering.","authors":"Herbert Kobald, Alexander M Kobald, Ivana Panzic, Marco Deluca","doi":"10.1038/s43246-024-00730-x","DOIUrl":null,"url":null,"abstract":"<p><p>Perovskites at the crossover between ferroelectric and relaxor are often used to realize dielectric capacitors with high energy and power density and simultaneously good efficiency. Lead-free Bi<sub>0.5</sub>Na<sub>0.5</sub>TiO<sub>3</sub> is gaining importance in showing an alternative to lead-based devices. Here we show that (<i>1-x</i>)Bi<sub>0.5</sub>Na<sub>0.5</sub>TiO<sub>3</sub> - <i>x</i>BaZr <sub><i>y</i></sub> Ti <sub><i>1-y</i></sub> O<sub>3</sub> (best: 0.94Bi<sub>0.5</sub>Na<sub>0.5</sub>TiO<sub>3</sub> -0.06BaZr<sub>0.4</sub>Ti<sub>0.6</sub>O<sub>3</sub>) shows an increase of recoverable energy density and electric breakdown upon chemical substitution. In thin films derived from Chemical Solution Deposition, we observed that polarization peaks at the morphotropic phase boundary at <i>x</i> = 0.06. While Zr substitution results in reduced polarization, it enhances both efficiency and electric breakdown strength, ultimately doubling the recoverable energy density and the metallization interface by lowering surface roughness. Our dielectric capacitor shows <3% deviation of energy properties over 10<sup>6</sup> cycles. A virtual device model of a multilayer thin film capacitor (7.25 mJ recoverable energy) was used to compare its performance to already in use multilayer ceramic capacitors.</p>","PeriodicalId":10589,"journal":{"name":"Communications Materials","volume":"6 1","pages":"12"},"PeriodicalIF":7.5000,"publicationDate":"2025-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11732744/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Communications Materials","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1038/s43246-024-00730-x","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/1/14 0:00:00","PubModel":"Epub","JCR":"Q1","JCRName":"MATERIALS SCIENCE, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0
Abstract
Perovskites at the crossover between ferroelectric and relaxor are often used to realize dielectric capacitors with high energy and power density and simultaneously good efficiency. Lead-free Bi0.5Na0.5TiO3 is gaining importance in showing an alternative to lead-based devices. Here we show that (1-x)Bi0.5Na0.5TiO3 - xBaZr y Ti 1-y O3 (best: 0.94Bi0.5Na0.5TiO3 -0.06BaZr0.4Ti0.6O3) shows an increase of recoverable energy density and electric breakdown upon chemical substitution. In thin films derived from Chemical Solution Deposition, we observed that polarization peaks at the morphotropic phase boundary at x = 0.06. While Zr substitution results in reduced polarization, it enhances both efficiency and electric breakdown strength, ultimately doubling the recoverable energy density and the metallization interface by lowering surface roughness. Our dielectric capacitor shows <3% deviation of energy properties over 106 cycles. A virtual device model of a multilayer thin film capacitor (7.25 mJ recoverable energy) was used to compare its performance to already in use multilayer ceramic capacitors.
期刊介绍:
Communications Materials, a selective open access journal within Nature Portfolio, is dedicated to publishing top-tier research, reviews, and commentary across all facets of materials science. The journal showcases significant advancements in specialized research areas, encompassing both fundamental and applied studies. Serving as an open access option for materials sciences, Communications Materials applies less stringent criteria for impact and significance compared to Nature-branded journals, including Nature Communications.