Demonstration of ultra-high recyclable energy densities in domain-engineered ferroelectric films

Dielectric capacitors have the highest charge/discharge speed among all electrical energy devices, but lag behind in energy density. Here we report dielectric ultracapacitors based on ferroelectric films of Ba(Zr 0.2 ,Ti 0.8 )O 3 which display high-energy densities (up to 166 J cm –3 ) and efficienc...

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Veröffentlicht in:Nature communications 2017-12, Vol.8 (1), p.1999-7, Article 1999
Hauptverfasser: Cheng, Hongbo, Ouyang, Jun, Zhang, Yun-Xiang, Ascienzo, David, Li, Yao, Zhao, Yu-Yao, Ren, Yuhang
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Sprache:eng
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Zusammenfassung:Dielectric capacitors have the highest charge/discharge speed among all electrical energy devices, but lag behind in energy density. Here we report dielectric ultracapacitors based on ferroelectric films of Ba(Zr 0.2 ,Ti 0.8 )O 3 which display high-energy densities (up to 166 J cm –3 ) and efficiencies (up to 96%). Different from a typical ferroelectric whose electric polarization is easily saturated, these Ba(Zr 0.2 ,Ti 0.8 )O 3 films display a much delayed saturation of the electric polarization, which increases continuously from nearly zero at remnant in a multipolar state, to a large value under the maximum electric field, leading to drastically improved recyclable energy densities. This is achieved by the creation of an adaptive nano-domain structure in these perovskite films via phase engineering and strain tuning. The lead-free Ba(Zr 0.2 ,Ti 0.8 )O 3 films also show excellent dielectric and energy storage performance over a broad frequency and temperature range. These findings may enable broader applications of dielectric capacitors in energy storage, conditioning, and conversion. Dielectric capacitors offer high-power delivery materials for energy-storage, yet suffer from low energy densities. Here, the authors prepared ferroelectric Ba(Zr 0.2 ,Ti 0.8 )O 3 that utilizes polydomain nanostructures to delay electric polarization saturation and boost energy densities.
ISSN:2041-1723
2041-1723
DOI:10.1038/s41467-017-02040-y