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Origin of UV-induced poling inhibition in lithium niobate crystals

Origin of UV-induced poling inhibition in lithium niobate crystals
Origin of UV-induced poling inhibition in lithium niobate crystals
Short-term exposure of the +z face of LiNbO3 crystals to focused UV laser light leads to persistent inhibition of ferroelectric domain reversal at the irradiated area, a phenomenon referred to as "poling inhibition." Different types of crystals (stoichiometric, congruent, or Mg-doped ones) are exposed, creating the so-called "latent state" and domain growth during subsequent electric-field poling is visualized. The latent state is robust against thermal annealing up to 250 °C and uniform illumination. With the tip of a scanning force microscope the coercive field is mapped, showing not only the expected resistance against domain reversal in the UV-irradiated region but also easier poling adjacent to the UV-irradiated section. These results and theoretical estimates point to the following mechanism of poling inhibition: the UV light-induced heating results in a local reduction of the lithium concentration, via thermodiffusion. The required charge compensation is provided by UV-excited free electrons/holes. After cooling, the lithium ions become immobile, and the reduced lithium concentration causes a strong local increase in the coercive field in the exposed area, while the increased Li concentration next to this area reduces the coercive field.
1550-235X
Steigerwald, H.
f5c7bc7e-a0db-4714-b2f0-1debd45b81be
Lilienblum, M.
4c84cf47-c9b1-471d-8ad5-72af67e2dea0
von Cube, F.
a3fcbc0c-37ef-4144-b179-b11ac98c0d5b
Ying, Y.J.
1cc13d62-ee04-4ca3-b0b8-e60a523dc145
Eason, R.W.
e38684c3-d18c-41b9-a4aa-def67283b020
Mailis, S.
233e0768-3f8d-430e-8fdf-92e6f4f6a0c4
Sturman, B.
f174421b-f538-4ee4-9f7d-64f9fe27e08d
Soergel, E.
f4d5aad1-9f81-4877-bceb-33ceed99d9d7
Buse, K.
ff6d2cb7-0e78-4382-adf0-239667447431
Steigerwald, H.
f5c7bc7e-a0db-4714-b2f0-1debd45b81be
Lilienblum, M.
4c84cf47-c9b1-471d-8ad5-72af67e2dea0
von Cube, F.
a3fcbc0c-37ef-4144-b179-b11ac98c0d5b
Ying, Y.J.
1cc13d62-ee04-4ca3-b0b8-e60a523dc145
Eason, R.W.
e38684c3-d18c-41b9-a4aa-def67283b020
Mailis, S.
233e0768-3f8d-430e-8fdf-92e6f4f6a0c4
Sturman, B.
f174421b-f538-4ee4-9f7d-64f9fe27e08d
Soergel, E.
f4d5aad1-9f81-4877-bceb-33ceed99d9d7
Buse, K.
ff6d2cb7-0e78-4382-adf0-239667447431

Steigerwald, H., Lilienblum, M., von Cube, F., Ying, Y.J., Eason, R.W., Mailis, S., Sturman, B., Soergel, E. and Buse, K. (2010) Origin of UV-induced poling inhibition in lithium niobate crystals. Physical Review B, 82 (21), [214105]. (doi:10.1103/PhysRevB.82.214105).

Record type: Article

Abstract

Short-term exposure of the +z face of LiNbO3 crystals to focused UV laser light leads to persistent inhibition of ferroelectric domain reversal at the irradiated area, a phenomenon referred to as "poling inhibition." Different types of crystals (stoichiometric, congruent, or Mg-doped ones) are exposed, creating the so-called "latent state" and domain growth during subsequent electric-field poling is visualized. The latent state is robust against thermal annealing up to 250 °C and uniform illumination. With the tip of a scanning force microscope the coercive field is mapped, showing not only the expected resistance against domain reversal in the UV-irradiated region but also easier poling adjacent to the UV-irradiated section. These results and theoretical estimates point to the following mechanism of poling inhibition: the UV light-induced heating results in a local reduction of the lithium concentration, via thermodiffusion. The required charge compensation is provided by UV-excited free electrons/holes. After cooling, the lithium ions become immobile, and the reduced lithium concentration causes a strong local increase in the coercive field in the exposed area, while the increased Li concentration next to this area reduces the coercive field.

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Published date: 1 December 2010

Identifiers

Local EPrints ID: 177065
URI: http://eprints.soton.ac.uk/id/eprint/177065
ISSN: 1550-235X
PURE UUID: 3a2743ac-1de8-4927-a991-d23822925d1a
ORCID for R.W. Eason: ORCID iD orcid.org/0000-0001-9704-2204
ORCID for S. Mailis: ORCID iD orcid.org/0000-0001-8100-2670

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Date deposited: 15 Mar 2011 09:06
Last modified: 15 Mar 2024 02:39

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Contributors

Author: H. Steigerwald
Author: M. Lilienblum
Author: F. von Cube
Author: Y.J. Ying
Author: R.W. Eason ORCID iD
Author: S. Mailis ORCID iD
Author: B. Sturman
Author: E. Soergel
Author: K. Buse

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