Nanodomain poling unlocking backward nonlinear light generation in thin film lithium niobate

Nonlinear frequency conversion offers powerful capabilities for applications in telecommunications, signal processing, and computing. Thin-film lithium niobate (TFLN) has emerged as a promising integrated photonics platform due to its strong electro-optic effect and second-order nonlinearity, which can be exploited through periodic poling. However, conventional poling techniques in x-cut TFLN are constrained to minimum period sizes on the order of microns, restricting access to highly phase-mismatched interactions such as counter- and backward-propagating frequency conversion. In this work, we demonstrate scalable periodic poling of x-cut TFLN with domains periods as short as 215 nm and realize devices that support both counter- and back-propagating phase matching. We estimate conversion efficiencies of 1,474 %/W/cm<sup>2</sup> and 45 %/W/cm<sup>2</sup> for the two interaction types, respectively. Sum frequency generation measurements confirm that the nonlinear generation takes place in the desired direction. Furthermore, we report spontaneous parametric down conversion for the counter-propagating configuration and, for the first time, for a backward propagating device. This breakthrough provides unprecedented control over engineering of ferroelectric domain geometries in TFLN, leading into the generation of photon pairs with precisely tailored spatial and spectral characteristics. Such capabilities hold strong potential for advancing quantum signal processing, scalable quantum computing architectures, and precision quantum metrology.

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Publication Details

Journal
Nanophotonics
Published
2025-12-01
DOI
https://doi.org/10.1515/nanoph-2025-0429
Primary Topic
Photorefractive and Nonlinear Optics
Type
article
Field-Weighted Citation Impact
0.00

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article

Nanodomain poling unlocking backward nonlinear light generation in thin film lithium niobate

Jost Kellner, Robert J. Chapman, Alessandra Sabatti, Rachel Grange
Nanophotonics
Photorefractive and Nonlinear Optics
article

Nanodomain poling unlocking backward nonlinear light generation in thin film lithium niobate

Jost Kellner, Robert J. Chapman, Alessandra Sabatti, Rachel Grange
article en

Abstract

Nonlinear frequency conversion offers powerful capabilities for applications in telecommunications, signal processing, and computing. Thin-film lithium niobate (TFLN) has emerged as a promising integrated photonics platform due to its strong electro-optic effect and second-order nonlinearity, which can be exploited through periodic poling. However, conventional poling techniques in x-cut TFLN are constrained to minimum period sizes on the order of microns, restricting access to highly phase-mismatched interactions such as counter- and backward-propagating frequency conversion. In this work, we demonstrate scalable periodic poling of x-cut TFLN with domains periods as short as 215 nm and realize devices that support both counter- and back-propagating phase matching. We estimate conversion efficiencies of 1,474 %/W/cm<sup>2</sup> and 45 %/W/cm<sup>2</sup> for the two interaction types, respectively. Sum frequency generation measurements confirm that the nonlinear generation takes place in the desired direction. Furthermore, we report spontaneous parametric down conversion for the counter-propagating configuration and, for the first time, for a backward propagating device. This breakthrough provides unprecedented control over engineering of ferroelectric domain geometries in TFLN, leading into the generation of photon pairs with precisely tailored spatial and spectral characteristics. Such capabilities hold strong potential for advancing quantum signal processing, scalable quantum computing architectures, and precision quantum metrology.

NanophotonicsVol. 14(26)
ETH Zurich (CH)
National Science Foundation, Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung, Eidgenössische Technische Hochschule Zürich
Openalex Percentile: Top 69%
Photorefractive and Nonlinear Optics
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