Phase Synergy Enables Low‐Power Ferroelectric Switching in HfO <sub>2</sub> Epitaxial Films

K Kefan Wang L Liyang Ma L Lijun Wu C Chuanrui Huo (Beijing Advanced Innovation Center for Materials Genome Engineering, Department of Physical Chemistry) S Sijie Zhu (School of Advanced Materials Innovation Innovation Center for Materials Genome Engineering University of Science and Technology Beijing Beijing China) C Chuhang Liu (Condensed Matter Physics and Materials Science Department, Brookhaven National Laboratory, Upton, NY, USA.) W Wen Sun (State Key Laboratory of Fine Chemicals, School of Chemical Engineering) W Weiwei Li (Beijing University of Chemical Technology , , ,) S Shi Liu (Department of Chemistry, School of Science and Research Center for Industries of the Future) Y Yimei Zhu (Condensed Matter Physics and Materials Science Department, Brookhaven National Laboratory, Upton, NY, USA.) S Shiqing Deng (Department of Physical Chemistry and Beijing Advanced Innovation Center for Materials Genome Engineering) J Jun Chen

Abstract

ABSTRACT HfO 2 ‐based ferroelectric materials have emerged as leading candidates for next‐generation non‐volatile memory technologies, owing to their nanoscale robust ferroelectricity and complementary metal–oxide–semiconductor (CMOS) compatibility. However, challenges and debates persist in advancing and comprehensively understanding their ferroelectric behavior. In particular, conventional approaches typically regard non‐ferroelectric phases as detrimental and primarily focus on suppressing their formation, yet overlooking their potentially synergistic contributions—particularly those of the tetragonal ( T ) phase. Here, we unambiguously clarify the beneficial role of the T ‐phase and introduce a phase‐boundary engineering strategy that deliberately harnesses it to enhance ferroelectricity in HfO 2 films. By stabilizing optimal coherent boundaries between ferroelectric orthorhombic ( O ) and T phases in epitaxial La‐doped HfO 2 films, we achieve significant improvements in ferroelectric properties—doubling the remanent polarization ( P r ∼ 30 µC/cm 2 ) and substantially reducing the coercive field ( E c ∼ 3 MV/cm) by 30% compared to low‐La doped samples without such boundaries. Atomic‐scale electron microscopy reveals the structural nature of the atomically sharp, coherent O – T boundaries. Combined with deep‐learning enhanced molecular dynamics simulations, our results unravel that these boundaries facilitate intermediate polarization states that lower the switching energy barrier. Consequently, phase coexistence shifts from an inherent drawback to a tunable design element, offering a broadly applicable route to ultra‐low‐power HfO 2 ‐based nanoelectronics.

Article Details

Volume / Issue Vol. 38, Issue 11
Published February 01, 2026
ISSN 0935-9648
Publisher Unknown Publisher

Journal Info

Advanced Materials

Unknown Publisher

ISSN: 0935-9648 Physical Sciences

Authors (12)

K

Kefan Wang

L

Liyang Ma

L

Lijun Wu

C

Chuanrui Huo

Beijing Advanced Innovation Center for Materials Genome Engineering, Department of Physical Chemistry

S

Sijie Zhu

School of Advanced Materials Innovation Innovation Center for Materials Genome Engineering University of Science and Technology Beijing Beijing China

C

Chuhang Liu

Condensed Matter Physics and Materials Science Department, Brookhaven National Laboratory, Upton, NY, USA.

W

Wen Sun

State Key Laboratory of Fine Chemicals, School of Chemical Engineering

W

Weiwei Li

Beijing University of Chemical Technology , , ,

S

Shi Liu

Department of Chemistry, School of Science and Research Center for Industries of the Future

Y

Yimei Zhu

Condensed Matter Physics and Materials Science Department, Brookhaven National Laboratory, Upton, NY, USA.

S

Shiqing Deng

Department of Physical Chemistry and Beijing Advanced Innovation Center for Materials Genome Engineering

J

Jun Chen