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Role of oxygen vacancies in stabilizing the orthorhombic phases of nanoparticles
Phys. Rev. B 114, 214111 – Published 27 October, 2026
DOI: https://doi.org/10.1103/4l86-w61k
Abstract
In this work we study the stabilization of the orthorhombic phases in small nanoparticles (average size ∼7 nm) annealed under different oxygen partial pressures. Concentration of the oxygen vacancies, which is determined by annealing conditions, was estimated from the electron paramagnetic resonance spectra and x-ray photoelectron spectroscopy. The fraction of the orthorhombic phases, that is determined by the x-ray diffraction and nuclear magnetic resonance, depends on the concentration of oxygen vacancies. Phenomenological calculations based on Landau-Ginzburg-Devonshire theory considering trilinear coupling between nonpolar, antipolar, and polar phonon modes, indicate that chemical strain induced by oxygen vacancies can stabilize the orthorhombic o-III phase with the ferroelectric long-range ordering in small nanoparticles. The theory confirms the stability of ferroelectric polarization in the vacancy-enriched nanoparticles. The increase in the intensity of the dielectric permittivity maximum observed near 350–380 K in a PVDF matrix embedded with nanoparticles annealed in the atmosphere is clearly associated with an increase in oxygen vacancy concentration. The vacancies lead to defect-induced elastic dipole formation and an increase in ionic conductivity, which decreases the depolarization field and may induce the ferroelectric-like phase transition in the vacancy-enriched nanoparticles. Due to the interfacial effects, the negative capacitance states may be realized in weakly screened and spatially isolated nanoparticles embedded in the PVDF matrix. The present approach based on oxygen-vacancy-induced elastic and screening effects may provide a route for engineering ferroelectric-like states in other nanoscale ferroic oxides.
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