Indirect but Efficient: Laser-Excited Electrons Can Drive Ultrafast Polarization Switching in Ferroelectric Materials

Abstract

To enhance the efficiency of next-generation ferroelectric (FE) electronic devices, new techniques for controlling ferroelectric polarization switching are required. While most prior studies have attempted to induce polarization switching via the excitation of phonons, these experimental techniques required intricate and expensive terahertz sources and have not been completely successful. Here, we propose a new mechanism for rapidly and efficiently switching the FE polarization via laser-tuning of the underlying dynamical potential energy surface. Using time-dependent density functional calculations, we observe an ultrafast switching of the FE polarization in BaTiO3 within 200 fs. A laser pulse can induce a charge density redistribution that reduces the original FE charge order. This excitation results in both desirable and highly directional ionic forces that are always opposite to the original FE displacements. Our new mechanism enables the reversible switching of the FE polarization with optical pulses that can be produced from existing 800 nm experimental laser sources.

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Cited by in corpus (7)

• Ultrafast reversal of the ferroelectric polarization by a midinfrared pulse
• Origin of Immediate Damping of Coherent Oscillations in Photoinduced Charge Density Wave Transition
• Ultrafast decoupling of polarization and strain in ferroelectric BaTiO${}_3$
• Dynamic Tilting of Ferroelectric Domain Walls via Optically Induced Electronic Screening
• Ferroelectric Polarization Reversal vs Pump Spot Shape
• Ultrafast non-thermal suppression of ferroelectricity by carrier screening in LiNbO3
• Large symmetry and hierarchical ordering transitions in sliding ferroelectrics