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

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...

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Bibliographic Details
Published in:The journal of physical chemistry letters Vol. 10; no. 12; pp. 3402 - 3407
Main Authors: Lian, Chao, Ali, Zulfikhar A, Kwon, Hyuna, Wong, Bryan M
Format: Journal Article
Language:English
Published: United States American Chemical Society 20-06-2019
Online Access:Get full text
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Summary: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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ISSN:1948-7185
1948-7185
DOI:10.1021/acs.jpclett.9b01046