TY - JOUR
T1 - Is There A Pure Electronic Ferroelectric?
AU - Wang, Xudong
AU - Teng, Guichen
AU - Meng, Xiangjian
AU - Cheng, Zhenxiang
AU - Lin, Tie
AU - Shen, Hao
AU - Wang, Xiaodan
AU - Wang, Jianlu
AU - Chu, Junhao
N1 - Publisher Copyright:
© 2025 The Author(s). Advanced Electronic Materials published by Wiley-VCH GmbH.
PY - 2026
Y1 - 2026
N2 - Different from traditional ferroelectrics whose polarization stems from ionic displacements mediated by phonons, electronic ferroelectrics exhibit spontaneous polarization originating from polar electronic ordering. Such electronic mechanisms promise devices with ultrafast switching speeds, lower energy consumption, and enhanced resilience to fatigue and depolarization fields inherent in conventional ferroelectrics. While early candidates are restricted to rare oxides and organic charge-transfer salts, emerging systems—particularly 2D van der Waals moiré heterostructures—have significantly broadened this materials landscape. This review comprehensively examines ferroelectrics governed by electronic mechanisms, categorizing them according to microscopic origins, including spin correlations, charge ordering, orbital interactions, charge-transfer instabilities, and excitonic phenomena. Representative materials span multiferroics, molecular crystals, and engineered van der Waals architectures. Crucially, we evaluate whether their ferroelectricity qualifies as purely electronic—defined by the absence of ionic displacements during polarization reversal—synthesizing recent theoretical and experimental advances to establish a unified framework for this evolving paradigm.
AB - Different from traditional ferroelectrics whose polarization stems from ionic displacements mediated by phonons, electronic ferroelectrics exhibit spontaneous polarization originating from polar electronic ordering. Such electronic mechanisms promise devices with ultrafast switching speeds, lower energy consumption, and enhanced resilience to fatigue and depolarization fields inherent in conventional ferroelectrics. While early candidates are restricted to rare oxides and organic charge-transfer salts, emerging systems—particularly 2D van der Waals moiré heterostructures—have significantly broadened this materials landscape. This review comprehensively examines ferroelectrics governed by electronic mechanisms, categorizing them according to microscopic origins, including spin correlations, charge ordering, orbital interactions, charge-transfer instabilities, and excitonic phenomena. Representative materials span multiferroics, molecular crystals, and engineered van der Waals architectures. Crucially, we evaluate whether their ferroelectricity qualifies as purely electronic—defined by the absence of ionic displacements during polarization reversal—synthesizing recent theoretical and experimental advances to establish a unified framework for this evolving paradigm.
KW - electronic ferroelectrics
KW - excitonic
KW - ionic displacements
KW - polar electronic ordering
KW - van der waals heterostructures
UR - https://www.scopus.com/pages/publications/105026410351
U2 - 10.1002/aelm.202500683
DO - 10.1002/aelm.202500683
M3 - 文献综述
AN - SCOPUS:105026410351
SN - 2199-160X
JO - Advanced Electronic Materials
JF - Advanced Electronic Materials
ER -