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

被引:182
作者
Cheng, Hongbo [1 ,2 ]
Ouyang, Jun [1 ,2 ,3 ,4 ]
Zhang, Yun-Xiang [1 ,2 ]
Ascienzo, David [3 ,4 ]
Li, Yao [1 ,2 ]
Zhao, Yu-Yao [1 ,2 ]
Ren, Yuhang [3 ,4 ]
机构
[1] Shandong Univ, Sch Mat Sci & Engn, Minist Educ, Key Lab Liquid Solid Struct Evolut & Proc Mat, Jinan 250061, Shandong, Peoples R China
[2] Shandong Univ, Suzhou Inst, Suzhou 215123, Peoples R China
[3] CUNY, Hunter Coll, Phys & Astron, New York, NY 10065 USA
[4] CUNY, Grad Ctr, 365 5th Ave, New York, NY 10016 USA
关键词
THIN-FILMS; POLYMER;
D O I
10.1038/s41467-017-02040-y
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
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.
引用
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页数:7
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