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author:

Bo Wu (Bo Wu.) [1] | Huijing Zheng (Huijing Zheng.) [2] | Yan-Qi Wu (Yan-Qi Wu.) [3] | Zhicheng Huang (Zhicheng Huang.) [4] | Hao-Cheng Thong (Hao-Cheng Thong.) [5] | Hong Tao (Hong Tao.) [6] | Jian Ma (Jian Ma.) [7] | Chunlin Zhao (Chunlin Zhao.) [8] | Ze Xu (Ze Xu.) [9] | Yi-Xuan Liu (Yi-Xuan Liu.) [10] | Zhipeng Xing (Zhipeng Xing.) [11] | Naixin Liang (Naixin Liang.) [12] | Fang-Zhou Yao (Fang-Zhou Yao.) [13] | Chao-Feng Wu (Chao-Feng Wu.) [14] | Ke Wang (Ke Wang.) [15] | Bing Han (Bing Han.) [16]

Abstract:

Despite the pivotal role of stannum doping in achieving ultrahigh piezoelectric performance in barium titanate-based ceramics, the fundamental mechanisms underlying this enhancement remain elusive. Here, we introduce a single variable nonstoichiometric stannum strategy in lead-free barium titanate-based ceramics with giant piezoelectricity, revealing that stannum doping contributes intrinsically and extrinsically to enhance piezoelectricity. Density functional theory calculations elucidate the intrinsic enhancement of polarization arising from lattice distortion and increased space for titanium-oxygen bonds induced by optimal stannum doping, which is corroborated by Rayleigh analysis. A phase transition from ferroelectric multiphase coexistence to paraelectric phase is observed, alongside a rapid miniaturized and eventually disappeared domains with increasing stannum doping. This evolution in phase structure and domain configuration induces a nearly vanishing polarization anisotropy and low domain wall energy, facilitating easy polarization rotation and domain wall motion, thereby significantly contributing to the extrinsic piezoelectric response. Consequently, the origins of ultrahigh performance can be attributed to the synergistic effect of stannum-induced intrinsic and extrinsic contributions in barium titanate-based ceramics. This study provides fundamental insights into the role of doping elements and offers guidance for the design of high-performance piezoelectrics.

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Nature Communications

ISSN: 2041-1723

Year: 2024

Issue: 1

Volume: 15

1 4 . 7 0 0

JCR@2023

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ESI Highly Cited Papers on the List: 0 Unfold All

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30 Days PV: 0

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