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Giant intrinsic electrocaloric effect in ferroelectrics by local structural engineering

Bo Wu, Hong Tao, Kui Chen, Zhipeng Xing, Yan-Qi Wu, Hao-Cheng Thong, Lin Zhao, Chunlin Zhao (), Ze Xu, Yi-Xuan Liu, Fang-Zhou Yao, Tianhang Zhou (), Jian Ma, Yan Wei (), Ke Wang and Shujun Zhang ()
Additional contact information
Bo Wu: Southwest Minzu University
Hong Tao: Southwest Minzu University
Kui Chen: Southwest Minzu University
Zhipeng Xing: Tsinghua University
Yan-Qi Wu: Tsinghua University
Hao-Cheng Thong: Tsinghua University
Lin Zhao: Southwest Minzu University
Chunlin Zhao: Fuzhou University
Ze Xu: Tsinghua University
Yi-Xuan Liu: Tsinghua University
Fang-Zhou Yao: Wuzhen Laboratory
Tianhang Zhou: China University of Petroleum (Beijing)
Jian Ma: Southwest Minzu University
Yan Wei: Peking University School and Hospital of Stomatology
Ke Wang: Tsinghua University
Shujun Zhang: University of Wollongong

Nature Communications, 2025, vol. 16, issue 1, 1-10

Abstract: Abstract The electrocaloric effect of ferroelectrics holds great promise for solid-state cooling, potentially replacing traditional vapor-compression refrigeration systems. However, achieving adequate electrocaloric cooling capacity at room temperature remains a formidable challenge due to the need for a high intrinsic electrocaloric effect. While barium titanate ceramic exhibits a pronounced electrocaloric effect near its Curie temperature, typical chemical modifications to enhance electrocaloric properties at room temperature often reduce this intrinsic electrocaloric effect. Herein, a structural design is introduced for barium titanate-based ceramics by incorporating isovalent cations. This leads to a well-ordered local structure that decreases the Curie temperature to room temperature while preserving a sharp phase transition, enabling a large dielectric constant and tunable polarization. This design achieves a remarkable electrocaloric strength of ~1.0 K·mm/kV, surpassing previous reports. Atomic-resolution structural analyses reveal that the presence of multiscale nanodomains (from ~10 nm to >100 nm), and the dipole polarization distribution with gradual dipole rotation enable rapid phase transition and facile polarization rotation, accounting for the giant electrocaloric response. This work provides a strategy for achieving a strong intrinsic electrocaloric effect in ferroelectrics near room temperature and offers key insights into the microstructure landscapes driving this enhanced electrocaloric effect.

Date: 2025
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DOI: 10.1038/s41467-025-61860-5

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