Author
Listed:
- Wen Di Zhang
(Fudan University)
- Zi Zheng Song
(The Hong Kong Polytechnic University
The Hong Kong Polytechnic University)
- Shu Qi Tang
(Fudan University)
- Jin Chen Wei
(Fudan University)
- Yan Cheng
(East China Normal University)
- Bing Li
(ShanghaiTech University)
- Shi You Chen
(Fudan University)
- Zi Bin Chen
(The Hong Kong Polytechnic University
The Hong Kong Polytechnic University)
- An Quan Jiang
(Fudan University
Fudan University)
Abstract
The ever-shrinking electrostatic capacitor, which is capable of storing substantial quantities of electrical charge, has found widespread applications in high-storage-density dynamic random access memory and energy-efficient complementary metal-oxide-semiconductor devices. Despite the high energy storage densities (133–152 J/cm3) and efficiencies (75–90%) that have been realized using relaxor ferroelectric thick films, low-permittivity interfacial layers in the ultrathin films have caused the overall permittivity to be one to two orders of magnitude lower than expected. However, innovative use of complementary metal-oxide-semiconductor-compatible HfO2-based materials with high permittivities (~52) could enable integration of these capacitors into few-nanometre-scale devices. This study reports an ultrahigh dielectric permittivity of 921, stored charge density of 349 μC/cm2, and energy density of 584 J/cm3 with nearly 100% efficiency within near-edge plasma-treated Hf0.5Zr0.5O2 thin-film capacitors when the Hf-based material’s ferroelectricity disappears suddenly after polarization fatigue. The ultrahigh dielectric permittivity originates from a distorted orthorhombic phase with ordered oxygen vacancies that enables high-density integration of extremely scaled logic and memory devices for low-voltage applications.
Suggested Citation
Wen Di Zhang & Zi Zheng Song & Shu Qi Tang & Jin Chen Wei & Yan Cheng & Bing Li & Shi You Chen & Zi Bin Chen & An Quan Jiang, 2025.
"Ultrahigh dielectric permittivity in Hf0.5Zr0.5O2 thin-film capacitors,"
Nature Communications, Nature, vol. 16(1), pages 1-10, December.
Handle:
RePEc:nat:natcom:v:16:y:2025:i:1:d:10.1038_s41467-025-57963-8
DOI: 10.1038/s41467-025-57963-8
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