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Quantum 2.0 Conference and Exhibition

Non-degenerate correlated SPDC photon source for UV-A illumination

Preetisha Goswami, Marta Gilaberte Basset, Jorge Fuenzalida, Markus Gräfe, Valerio Flavio Gili

Published Jan 1, 2024• 0 citations
Publisher

Abstract

We present a correlated photon source consisting of a BBO nonlinear crystal that generates ultraviolet UV-A and infrared light via SPDC. Quantum imaging and sensing techniques can benefit from the correlations between the down-converted beams.
DOI
10.1364/quantum.2024.qw3a.2

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We present a frequency-correlated non-degenerate photon-pair source consisting of a second-order nonlinear crystal that generates ultraviolet UV-A and infrared light via spontaneous parametric down-conversion (SPDC). Quantum imaging and sensing techniques like quantum imaging with undetected light and quantum ghost imaging leverage wavelength correlations between down-converted photon pairs to decouple sensing and detection wavelengths, thereby exploiting established camera technology within the visible spectrum. Our results open up quantum sensing application scenarios in the ultraviolet domain, with potential implications for advancements in biomedical and non-destructive testing fields.
Quantum states of light are opening new paradigm for imaging, enabling imaging with photons that didn’t interact with the object. Quantum imaging methods discussed here explore quantum correlated photon pairs, generated via spontaneous parametric down conversion (SPDC) in the nonlinear crystal (NLC). We demonstrate generation of highly non-degenerate photon pairs, via SPDC in AGS crystal, with the photon interacting with the object in the mid-infrared (MIR) and the non-interacting in the near-infrared spectral region. Results revealed that the wavelength of the interacting photon can be tuned in a wide spectral range, between 5 μm and 11 μm, covering most of "fingerprint" spectral region. This makes quantum imaging with AGS an alternative to more costly FTIR spectrometers.
The recent advent of optical metasurfaces, ultra-thin structures composed of nanoresonators facilitating strong light concentration [1–3], opens the path towards efficient \nfrequency conversion [4–7] in a material thousand times thinner than a human hair [8]. \nThere is a remarkable capacity to individually shape each nanoresonator of the metasurface to spatially and spectrally control the conversion process with unprecedented \nnanoscale resolution, facilitating an ultimate flexibility to selectively convert, focus, \nand image different colours with a single metasurface. The strong enhancement of the \nnonlinear processes in dielectric nanoresonators is largely due to the absence of material \nabsorption and the excitation of Mie-type bulk resonances [2]. The highest conversion \nefficiency to date has been achieved employing III-V semiconductor nanostructures, \nsuch as AlGaAs which is a non-centrosymmetric material with high quadratic nonlinear \nsusceptibility. In particular, second-harmonic generation efficiencies up to 10−4 have \nbeen recently demonstrated [8–12], six orders of magnitude higher than in plasmonics. \nSuch capabilities can make an immense fundamental and practical impact, including \nthe quantum state generation in nonlinear metasurfaces as we discuss in this chapter. \nThe quantum state of correlated photon-pairs is the essential building block for photon entanglement [13, 14], which underpins many quantum applications, including secure networks, enhanced measurement and lithography, and quantum information processing [15]. One of the most versatile techniques for the generation of correlated photons is the process of spontaneous parametric down-conversion (SPDC) [16, 17], see \nFig. 1. It allows for an arbitrary choice of energy and momentum correlations between \nthe generated photons, robust operation at room temperature, as well as for spatial and \ntemporal coherence between simultaneously pumped multiple SPDC sources. Alternative approaches based on atom-like single photon emitters, such as solid-state fluorescent atomic defects [18], quantum dots [19, 20], and 2D host materials [21, 22], have \nreached a high degree of frequency indistinguishability, purity and brightness [19, 20]. \nHowever, this comes with the expense of operation at cryogenic temperatures and lack \nof spatial coherence between multiple quantum emitters. These features might limit \npossible applications and reduce the potential for device scalability. Furthermore, the \nsmall size of the atomic sources often requires complex schemes aimed at coupling to \noptical nanoantennas and improving the photon extraction efficiency [21]. \nThe miniaturization of SPDC quantum-light sources to micro and nanoscale dimensions is a continuing quest, as it enables denser integration of functional quantum \ndevices. Traditionally, bulky cm-sized crystals were utilized for SPDC, entailing the \ndifficulty of aligning multiple optical elements after the SPDC crystal, while offering \nrelatively low photon-pair rates [17]. As a first step of miniaturization, SPDC was \nrealized in low-index-contrast waveguides, which allowed confining light down to several square micrometers transversely to the propagation direction, significantly enhancing the conversion efficiency [23]. However, this approach still requires centimetres \nof propagation length, which makes the on-chip integration with other elements challenging [24]. The introduction of high-index contrast waveguides and ring resonators \nallowed for shrinking the sizes necessary for SPDC to millimetres [25], and to tens \nof micrometers [26]. However, further miniaturisation down to the metasurfaces composed of nanoresonators requires conceptually different approaches.
Autocorrelation is a common method to estimate the duration of ultrashort laser pulses. In the ultraviolet (UV) regime it is challenging to employ the process of second-harmonic generation, most prominently due to absorption in nonlinear crystals at very short wavelengths. Here we show how to utilize spontaneous parametric down-conversion (SPDC) to generate an autocorrelation signal in the infrared (IR) for UV pulses. Our method utilizes the nth-order emission of the SPDC process, which occurs for low pumping powers proportional to the nth power of the UV intensity. Thus, counting 2n down-converted photons directly yields the nth-order autocorrelation. The method, now with detection of near-IR photons, is applied to the first direct measurement of ultrashort UV pulses circulating inside a UV enhancement cavity.