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Applied Physics Letters

Interferometric two-photon-absorption spectroscopy with three entangled photons

Lyuzhou Ye, Shaul Mukamel

Published Apr 27, 2020• 10 citations
Publisher

Abstract

We propose an interferometric pump-probe technique that employs three entangled photons generated by cascaded spontaneous parametric downconversion. A Mach–Zehnder interferometer made of two three-port waveguide arrays is inserted in the optical path. Two independent phases introduced to manipulate the entangled photon state serve as control parameters and can selectively excite matter pathways. Compared to two-photon-absorption of an entangled photon-pair, the three-photon signals are significantly enhanced by frequency-dispersed photon-counting detection.

DOI
10.1063/5.0004617

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We propose an interferometric pump-probe technique that employs three entangled photons generated by cascaded spontaneous parametric downconversion. A Mach–Zehnder interferometer made of two three-port waveguide arrays is inserted in the optical path. Two independent phases introduced to manipulate the entangled photon state serve as control parameters and can selectively excite matter pathways. Compared to two-photon-absorption of an entangled photon-pair, the three-photon signals are significantly enhanced by frequency-dispersed photon-counting detection.
We introduce optical lock-in detection in coincidence photon counting to enhance the extraction of information in “quantum-light spectroscopy”, based on using time-frequency entangled photon pairs to probe a molecular sample. The sample is placed inside a Mach-Zehnder interferometer, into which photons are injected and detected in coincidence at the interferometer output. Clear signatures of two-photon interference (both ‘Hong-Ou-Mandel’ and ‘N00N’) are observed and separated into distinct information channels. In addition to achieving an increased signal-to-noise ratio (SNR) at low count rates, the experiment uses a “down-sampling” technique that increases the efficiency of data collection by an order of magnitude.
Abstract The authors demonstrate a form of two‐photon‐counting interferometry by measuring the coincidence counts between single‐photon‐counting detectors at an output port of a Mach–Zehnder Interferometer (MZI) following injection of broad‐band time‐frequency‐entangled photon pairs (EPP) generated from collinear spontaneous parametric down conversion into a single input port. Spectroscopy and refractometry are performed on a sample inserted in one internal path of the MZI by scanning the other path in length, which acquires phase and amplitude information about the sample's linear response. Phase modulation and lock‐in detection are introduced to increase detection signal‐to‐noise ratio and implement a “down‐sampling” technique for scanning the interferometer delay, which reduces the sampling requirements needed to reproduce fully the temporal interference pattern. The phase‐modulation technique also allows the contributions of various quantum‐state pathways leading to the final detection outcomes to be extracted individually. Feynman diagrams frequently used in the context of molecular spectroscopy are used to describe the interferences resulting from the coherence properties of time‐frequency EPPs passing through the MZI. These results are an important step toward the implementation of a proposed method for molecular spectroscopy—quantum‐light‐enhanced 2D spectroscopy.
The application of quantum states of light such as entangled photons, for example, created by parametric down conversion, has experienced tremendous progress in the almost 40 years since their first experimental realization. Initially, they were employed in the investigation of the foundations of quantum physics, such as the violation of Bell's inequalities and studies of quantum entanglement. They later emerged as basic platforms for quantum communication protocols and, in the recent experiments on single-photon interactions, in photonic quantum computation. These applications aim at the controlled manipulation of the photonic degrees of freedom, and therefore rely on simple models of matter, where the analysis is simpler. Furthermore, quantum imaging with entangled light can achieve enhanced resolution, and quantum metrology can overcome the shot noise limit for classical light. This Account focuses on an entirely different emerging class of applications using quantum light as a powerful spectroscopic tool to reveal novel information about complex molecules. These applications utilize two appealing properties of quantum light: its distinct intensity fluctuations and its nonclassical bandwidth properties. These give rise to new and surprising behavior of nonlinear optical signals. Nonclassical intensity fluctuations can enhance nonlinear optical signals relative to linear absorption. For instance, the two-photon absorption of entangled photon pairs scales linearly (rather than quadratically) in the photon flux, just like a single photon absorption. This enables nonlinear quantum spectroscopy of photosensitive, for example, biological, samples at low light intensities. We will discuss how the two-photon absorption cross section becomes a function of the photonic quantum state, which can be manipulated by properties of the entangled photon pairs. In addition, the quantum correlations in entangled photon states further influence the nonlinear signals in a variety of ways. Apart from affecting the signal's scaling with intensity, they also constitute an entirely new approach to shaping and controlling excitation pathways in molecular aggregates in a way that cannot be achieved with shaped classical pulses. This is because between the two absorption events in entangled two-photon absorption, the light and material system are entangled. Classical constraints for the simultaneous time and frequency resolution can thus be circumvented, since the two are not Fourier conjugates. Here we review the simplest manifestation of quantum light spectroscopy, two-photon absorption spectroscopy with entangled photons. This will allow us to discuss exemplarily the impact of quantum properties of light on a nonlinear optical signal and explore the opportunities for future applications.
In this paper, we propose an integrated optic waveguide device employing a modified Mach–Zehnder interferometer, capable of generating nondegenerate, hyperentangled photon pairs. The geometry enables multiple (eight) type-II phase-matched spontaneous parametric downconversion processes simultaneously, resulting in a biphoton state, which is simultaneously entangled in polarization and spatial modes. Using an electro-optic phase modulator, we show the possibility of altering modal entanglement without affecting polarization entanglement. Such switchable, maximally entangled photon pairs, entangled in multiple degrees of freedom, should be very useful in various on-chip quantum optics experiments and in the implementation of quantum information protocols employing higher dimensional entanglement.
Recent advances in techniques for generating quantum light have stimulated research on novel spectroscopic measurements using quantum entangled photons. One such spectroscopy technique utilizes non-classical correlations among entangled photons to enable measurements with enhanced sensitivity and selectivity. Here, we investigate the spectroscopic measurement utilizing entangled three photons. In this measurement, time-resolved entangled photon spectroscopy with monochromatic pumping [A. Ishizaki, J. Chem. Phys. 153, 051102 (2020)] is integrated with the frequency-dispersed two-photon counting technique, which suppresses undesired accidental photon counts in the detector and thus allows one to separate the weak desired signal. This time-resolved frequency-dispersed two-photon counting signal, which is a function of two frequencies, is shown to provide the same information as that of coherent two-dimensional optical spectra. The spectral distribution of the phase-matching function works as a frequency filter to selectively resolve a specific region of the two-dimensional spectra, whereas the excited-state dynamics under investigation are temporally resolved in the time region longer than the entanglement time. The signal is not subject to Fourier limitations on the joint temporal and spectral resolution, and therefore, it is expected to be useful for investigating complex molecular systems in which multiple electronic states are present within a narrow energy range.