Highly directive antennas with the ability of shaping radiation patterns in desired directions are essential for efficient on-chip optical communication with reduced cross talk. In this paper, we design and optimize three distinct broadband traveling-wave tantalum pentoxide antennas exhibiting highly directional characteristics. Our antennas contain a director and reflector deposited on a glass substrate, which are excited by a dipole emitter placed in the feed gap between the two elements. Full-wave simulations in conjunction with global optimization provide structures with an enhanced linear directivity as high as 119 radiating in the substrate. The high directivity is a result of the interplay between two dominant TE modes and the leaky modes present in the antenna director. Furthermore, these low-loss dielectric antennas exhibit a near-unity radiation efficiency at the operational wavelength of 780 nm and maintain a broad bandwidth. Our numerical results are in good agreement with experimental measurements from the optimized antennas fabricated using a two-step electron-beam lithography, revealing the highly directive nature of our structures. We envision that our antenna designs can be conveniently adapted to other dielectric materials and prove instrumental for inter-chip optical communications and other on-chip applications.

<jats:title>Abstract</jats:title> <jats:p>Lithium niobate is a promising platform for integrated quantum optics. In this platform, we aim to efficiently manipulate and detect quantum states by combining superconducting single photon detectors and modulators. The cryogenic operation of a superconducting single photon detector dictates the optimisation of the electro-optic modulators under the same operating conditions. To that end, we characterise a phase modulator, directional coupler, and polarisation converter at both ambient and cryogenic temperatures. The operation voltage <jats:inline-formula> <jats:tex-math><?CDATA $V_{\pi/2}$?></jats:tex-math> <mml:math xmlns:mml="http://www.w3.org/1998/Math/MathML" overflow="scroll"> <mml:msub> <mml:mi>V</mml:mi> <mml:mrow> <mml:mi>π</mml:mi> <mml:mrow> <mml:mo>/</mml:mo> </mml:mrow> <mml:mn>2</mml:mn> </mml:mrow> </mml:msub> </mml:math> <jats:inline-graphic xmlns:xlink="http://www.w3.org/1999/xlink" xlink:href="jpphotonac6c63ieqn1.gif" xlink:type="simple" /> </jats:inline-formula> of these modulators increases, due to the decrease in the electro-optic effect, by 74% for the phase modulator, 84% for the directional coupler and 35% for the polarisation converter below 8.5<jats:inline-formula> <jats:tex-math><?CDATA $\,\mathrm{K}$?></jats:tex-math> <mml:math xmlns:mml="http://www.w3.org/1998/Math/MathML" overflow="scroll"> <mml:mrow> <mml:mi mathvariant="normal">K</mml:mi> </mml:mrow> </mml:math> <jats:inline-graphic xmlns:xlink="http://www.w3.org/1999/xlink" xlink:href="jpphotonac6c63ieqn2.gif" xlink:type="simple" /> </jats:inline-formula>. The phase modulator preserves its broadband nature and modulates light in the characterised wavelength range. The unbiased bar state of the directional coupler changed by a wavelength shift of 85<jats:inline-formula> <jats:tex-math><?CDATA $\,\mathrm{nm}$?></jats:tex-math> <mml:math xmlns:mml="http://www.w3.org/1998/Math/MathML" overflow="scroll"> <mml:mrow> <mml:mi mathvariant="normal">n</mml:mi> <mml:mi mathvariant="normal">m</mml:mi> </mml:mrow> </mml:math> <jats:inline-graphic xmlns:xlink="http://www.w3.org/1999/xlink" xlink:href="jpphotonac6c63ieqn3.gif" xlink:type="simple" /> </jats:inline-formula> while cooling the device down to 5<jats:inline-formula> <jats:tex-math><?CDATA $\,\mathrm{K}$?></jats:tex-math> <mml:math xmlns:mml="http://www.w3.org/1998/Math/MathML" overflow="scroll"> <mml:mrow> <mml:mi mathvariant="normal">K</mml:mi> </mml:mrow> </mml:math> <jats:inline-graphic xmlns:xlink="http://www.w3.org/1999/xlink" xlink:href="jpphotonac6c63ieqn4.gif" xlink:type="simple" /> </jats:inline-formula>. The polarisation converter uses periodic poling to phasematch the two orthogonal polarisations. The phasematched wavelength of the utilised poling changes by 112<jats:inline-formula> <jats:tex-math><?CDATA $\,\mathrm{nm}$?></jats:tex-math> <mml:math xmlns:mml="http://www.w3.org/1998/Math/MathML" overflow="scroll"> <mml:mrow> <mml:mi mathvariant="normal">n</mml:mi> <mml:mi mathvariant="normal">m</mml:mi> </mml:mrow> </mml:math> <jats:inline-graphic xmlns:xlink="http://www.w3.org/1999/xlink" xlink:href="jpphotonac6c63ieqn5.gif" xlink:type="simple" /> </jats:inline-formula> when cooling to 5<jats:inline-formula> <jats:tex-math><?CDATA $\,\mathrm{K}$?></jats:tex-math> <mml:math xmlns:mml="http://www.w3.org/1998/Math/MathML" overflow="scroll"> <mml:mrow> <mml:mi mathvariant="normal">K</mml:mi> </mml:mrow> </mml:math> <jats:inline-graphic xmlns:xlink="http://www.w3.org/1999/xlink" xlink:href="jpphotonac6c63ieqn6.gif" xlink:type="simple" /> </jats:inline-formula>.</jats:p>

We study the DC conductivity in potassium titanyl phosphate (KTiOPO4, KTP) and its isomorphs KTiOAsO4 (KTA) and Rb1%K99%TiOPO4 (RKTP) and introduce a method by which to reduce the overall ionic conductivity in KTP by a potassium nitrate treatment. Furthermore, we create so-called gray tracking in KTP and investigate the ionic conductivity in theses areas. A local unintended reduction of the ionic conductivity is observed in the gray-tracked regions, which also induce additional optical absorption in the material. We show that a thermal treatment in an oxygen-rich atmosphere removes the gray tracking and brings the ionic conductivity as well as the optical transmission back to the original level. These studies can help to choose the best material and treatment for specific applications.

<jats:p>Potassium titanyl phosphate (KTP) is a nonlinear optical material with applications in high-power frequency conversion or quasi-phase matching in submicron period domain grids. A prerequisite for these applications is a precise control and understanding of the poling mechanisms to enable the fabrication of high-grade domain grids. In contrast to the widely used material lithium niobate, the domain growth in KTP is less studied, because many standard methods, such as selective etching or polarization microscopy, provides less insight or are not applicable on non-polar surfaces, respectively. In this work, we present results of confocal Raman-spectroscopy of the ferroelectric domain structure in KTP. This analytical method allows for the visualization of domain grids of the non-polar KTP y-face and therefore more insight into the domain-growth and -structure in KTP, which can be used for improved domain fabrication.</jats:p>

We demonstrate the integration of amorphous tungsten silicide superconducting nanowire single-photon detectors on titanium in-diffused lithium niobate waveguides. We show proof-of-principle detection of evanescently coupled photons of 1550 nm wavelength using bidirectional waveguide coupling for two orthogonal polarization directions. We investigate the internal detection efficiency as well as detector absorption using coupling-independent characterization measurements. Furthermore, we describe strategies to improve the yield and efficiency of these devices.

Polarons in dielectric crystals play a crucial role for applications in integrated electronics and optoelectronics. In this work, we use density-functional theory and Green's function methods to explore the microscopic structure and spectroscopic signatures of electron polarons in lithium niobate (LiNbO3). Total-energy calculations and the comparison of calculated electron paramagnetic resonance data with available measurements reveal the formation of bound polarons at Nb_Li antisite defects with a quasi-Jahn-Teller distorted, tilted configuration. The defect-formation energies further indicate that (bi)polarons may form not only at Nb_Li antisites but also at structures where the antisite Nb atom moves into a neighboring empty oxygen octahedron. Based on these structure models, and on the calculated charge-transition levels and potential-energy barriers, we propose two mechanisms for the optical and thermal splitting of bipolarons, which provide a natural explanation for the reported two-path recombination of bipolarons. Optical-response calculations based on the Bethe-Salpeter equation, in combination with available experimental data and new measurements of the optical absorption spectrum, further corroborate the geometries proposed here for free and defect-bound (bi)polarons.

<jats:p>An integrated chip with quantum state generation, active polarization manipulation, and precise time control is demonstrated.</jats:p>

In recent years, Raman spectroscopy has been used to visualize and analyze ferroelectric domain structures. The technique makes use of the fact that the intensity or frequency of certain phonons is strongly influenced by the presence of domain walls. Although the method is used frequently, the underlying mechanism responsible for the changes in the spectra is not fully understood. This inhibits deeper analysis of domain structures based on this method. Two different models have been proposed. However, neither model completely explains all observations. In this work, we have systematically investigated domain walls in different scattering geometries with Raman spectroscopy in the common ferroelectric materials used in integrated optics, i.e., KTiOPO4, LiNbO3, and LiTaO3. Based on the two models, we can demonstrate that the observed contrast for domain walls is in fact based on two different effects. We can identify on the one hand microscopic changes at the domain wall, e.g., strain and electric fields, and on the other hand a macroscopic change of selection rules at the domain wall. While the macroscopic relaxation of selection rules can be explained by the directional dispersion of the phonons in agreement with previous propositions, the microscopic changes can be explained qualitatively in terms of a simplified atomistic model.