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通过畴工程实现基于铁酸铋的薄膜电容器的超高能量密度和高效率。

Giant energy density and high efficiency achieved in bismuth ferrite-based film capacitors via domain engineering.

机构信息

State Key Laboratory of New Ceramics and Fine Processing, School of Materials Science and Engineering, Tsinghua University, Beijing, 100084, China.

Beijing National Laboratory for Condensed Matter Physics, Institute of Physics, Chinese Academy of Sciences, Beijing, 100190, China.

出版信息

Nat Commun. 2018 May 8;9(1):1813. doi: 10.1038/s41467-018-04189-6.

Abstract

Developing high-performance film dielectrics for capacitive energy storage has been a great challenge for modern electrical devices. Despite good results obtained in lead titanate-based dielectrics, lead-free alternatives are strongly desirable due to environmental concerns. Here we demonstrate that giant energy densities of ~70 J cm, together with high efficiency as well as excellent cycling and thermal stability, can be achieved in lead-free bismuth ferrite-strontium titanate solid-solution films through domain engineering. It is revealed that the incorporation of strontium titanate transforms the ferroelectric micro-domains of bismuth ferrite into highly-dynamic polar nano-regions, resulting in a ferroelectric to relaxor-ferroelectric transition with concurrently improved energy density and efficiency. Additionally, the introduction of strontium titanate greatly improves the electrical insulation and breakdown strength of the films by suppressing the formation of oxygen vacancies. This work opens up a feasible and propagable route, i.e., domain engineering, to systematically develop new lead-free dielectrics for energy storage.

摘要

开发用于电容储能的高性能薄膜电介质一直是现代电子设备面临的巨大挑战。尽管基于钛酸铅的电介质已经取得了良好的效果,但由于环境问题,强烈需要无铅替代品。在这里,我们通过畴工程证明,通过畴工程可以在无铅的铋铁氧体-钛酸锶固溶体薄膜中实现~70 J/cm 的巨大能量密度,以及高效率、优异的循环和热稳定性。研究表明,钛酸锶的掺入将铋铁氧体的铁电微畴转化为高度动态的极性纳米区,从而导致铁电到弛豫铁电的转变,同时提高了能量密度和效率。此外,通过抑制氧空位的形成,钛酸锶的引入极大地提高了薄膜的电绝缘和击穿强度。这项工作为开发用于储能的新型无铅电介质提供了一条可行且可推广的途径,即畴工程。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/385c/5940880/d646ce1c8da8/41467_2018_4189_Fig1_HTML.jpg

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