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F. Eilenberger

Publications and source records attributed to F. Eilenberger.

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Hybrid Barium Titanate Waveguide Designs For Efficient Nonlinear Frequency Conversion

Barium titanate (BaTiO$_3$) is emerging as a powerful integrated photonic material, combining strong $X^{(2)}$ and electro-optic nonlinearities with rapidly improving thin-film waveguide quality. Recent demonstrations of low-loss BaTiO$_3$ waveguides and high-Q resonators have established BaTiO$_3$-on-insulator as a promising platform for next-generation frequency-conversion and quantum photonic technologies. However, while BaTiO$_3$ electro-optic modulators are now well developed, nonlinear BaTiO$_3$ waveguide engineering remains comparatively immature. Techniques widely used in lithium niobate, such as periodic poling for quasi-phase-matching, are poorly suited to BaTiO$_3$ because epitaxial thin films exhibit high coercive fields, strong strain-clamping effects, multivariant domain structures, and slow, complex switching dynamics. These factors make accurate periodic poling challenging and hinder the development of efficient $X^{(2)}$ frequency converters. Here, we introduce a fabrication-robust alternative based on linear-nonlinear hybrid waveguides, where TiO$_2$ is selectively incorporated into BaTiO$_3$ ridge waveguides to enhance nonlinear mode overlap while relying solely on modal phase-matching. Using coupled-mode-theory simulations, we identify phase-matched geometries and show that the hybrid design achieves a 2.75x increase in normalized second harmonic generation efficiency over monolithic BaTiO$_3$ waveguides. The uniform, lithographically defined cross-section makes the approach highly scalable. These results position hybrid BaTiO$_3$-TiO$_2$ waveguides as a practical route to CMOS-compatible, high-efficiency $X^{(2)}$ devices for integrated quantum photonics.

physics.optics

Demonstration of a polariton step potential by local variation of light-matter coupling in a van-der-Waals heterostructure

The large oscillator strength of excitons in transition metal dichalcogenide layers facilitates the formation of exciton-polariton resonances for monolayers and van-der-Waals heterostructures embedded in optical microcavities. Here, we show, that locally changing the number of layers in a WSe2/hBN/WSe2 van-der-Waals heterostructure embedded in a monolithic, high-quality-factor cavity gives rise to a local variation of the coupling strength. This effect yields a polaritonic stair case potential, which we demonstrate at room temperature. Our result paves the way towards engineering local polaritonic potentials at length scales down to atomically sharp interfaces, based on purely modifying its real part contribution via the coherent light-matter coupling strength g.

cond-mat.mes-hall