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Quantum Optical Metrology Using Two-Photon Interference

Kyle Jordan

Published Jan 22, 2026• 0 citations
Publisher

Abstract

Optical quantum metrology uses specially-prepared states of light to probe sensitive samples. Choosing a suitable probe state allows one to extract more information per probe photon about an unknown parameter than is possible using any classical technique. In effect, these techniques improve the sensitivity of the measurement whenever the number of probe photons is constrained in some way. This thesis presents experimental and theoretical results on the use of pairs of time-frequency entangled photons in precision measurements. It begins with an overview of necessary background knowledge about quantum optics and quantum information. This is followed by a theoretical discussion on the estimation of a single delay using two-photon interference. We show that constraints on the probe photon's bandwidth complicate the measurement problem, requiring suitable optimization of the two-photon quantum state to avoid losing precision. We then consider the use of two-photon interference for linear spectroscopic measurements. Linear spectroscopy relates the absorption and phase spectrum of a sample to unknown electronic parameters. We describe a proof-of-principle experiment demonstrating that two-photon interferometric spectroscopy can be used for simultaneously measurement of both absorption and phase. This is followed by an information-theoretic discussion of the precision of this technique. For low losses, we show that the method provides phase sensitivity similar to classical interferometry while approaching the optimal absorption precision of any possible measurement. If the absorption and phase values are both related to a single unknown parameter, then our technique provides improved sensitivity to this parameter compared to both classical measurements and other quantum techniques in the presence of realistic levels of loss. We conclude with a discussion of quantum-optical coherence tomography, which is a two-photon interferometric method for determining the material structure of a sample. We present an ongoing experiment which aims to apply the method to tissue-like samples, where the quantum measurement is limited by a poor signal-to-noise ratio. Preliminary results demonstrate that this noise can be largely reduced by suitable frequency-domain filtering. This allows us to precisely determine the position of a scattering center using a few hundred detected photon pairs despite the presence of large amounts of noise. We follow this with a theoretical discussion of signal artifacts which are known to complicate the measured interferogram. We show these artifacts are due to a distinct interferometric effect, which can be distinguished from the signal of interest using the relative time delay between detected photons. We conclude with a brief discussion on possible techniques for artifact removal.

DOI
10.20381/ruor-31696

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Optical quantum metrology uses specially-prepared states of light to probe sensitive samples. Choosing a suitable probe state allows one to extract more information per probe photon about an unknown parameter than is possible using any classical technique. In effect, these techniques improve the sensitivity of the measurement whenever the number of probe photons is constrained in some way. This thesis presents experimental and theoretical results on the use of pairs of time-frequency entangled photons in precision measurements. It begins with an overview of necessary background knowledge about quantum optics and quantum information. This is followed by a theoretical discussion on the estimation of a single delay using two-photon interference. We show that constraints on the probe photon's bandwidth complicate the measurement problem, requiring suitable optimization of the two-photon quantum state to avoid losing precision. We then consider the use of two-photon interference for linear spectroscopic measurements. Linear spectroscopy relates the absorption and phase spectrum of a sample to unknown electronic parameters. We describe a proof-of-principle experiment demonstrating that two-photon interferometric spectroscopy can be used for simultaneously measurement of both absorption and phase. This is followed by an information-theoretic discussion of the precision of this technique. For low losses, we show that the method provides phase sensitivity similar to classical interferometry while approaching the optimal absorption precision of any possible measurement. If the absorption and phase values are both related to a single unknown parameter, then our technique provides improved sensitivity to this parameter compared to both classical measurements and other quantum techniques in the presence of realistic levels of loss. We conclude with a discussion of quantum-optical coherence tomography, which is a two-photon interferometric method for determining the material structure of a sample. We present an ongoing experiment which aims to apply the method to tissue-like samples, where the quantum measurement is limited by a poor signal-to-noise ratio. Preliminary results demonstrate that this noise can be largely reduced by suitable frequency-domain filtering. This allows us to precisely determine the position of a scattering center using a few hundred detected photon pairs despite the presence of large amounts of noise. We follow this with a theoretical discussion of signal artifacts which are known to complicate the measured interferogram. We show these artifacts are due to a distinct interferometric effect, which can be distinguished from the signal of interest using the relative time delay between detected photons. We conclude with a brief discussion on possible techniques for artifact removal.
Quantum spectroscopy seeks to probe chemical systems using nonclassical light, which has properties that are qualitatively and quantitatively different than conventional light sources. One promising technique uses intensity-correlated twin beams of light to reduce the noise sources inherent to absorption spectroscopy. However, measurements of the phase shift imparted by the chemical sample, which provides complementary information to the absorption, continue to be a challenge. Here, we propose and demonstrate a scheme using entangled photon pairs that can simultaneously measure both the absorption and phase shift of a sample with extremely low optical intensities and with relatively fast few-minute acquisition times. This method combines the previous use of intensity correlations with a broadband quantum interferometer utilizing two-photon interference to measure the complete linear optical response of the sample. Our work shows that precise measurements of absorption can also be made phase-sensitive using suitable choices of probe beam and detection scheme. This enables a new class of quantum spectroscopy schemes which measure absorption and phase with a single probe. Our technique is relevant to the characterization of a wide array of chemical and biological samples, such as quantum dots and organic fluorophores, and may be useful for spectroscopic measurements that are otherwise constrained in intensity.
With the rapid development of quantum technologies in recent years, the need for high-sensitivity measuring techniques has become a key issue. In particular, optical sensors based on quantum states of light have proven to be optimal resources for high-precision interferometry. Nevertheless, their performance may be severely affected by the presence of noise or imperfections. In this work, we derive the quantum Fisher information matrix associated with the simultaneous estimation of an interferometric phase and the indistinguishability characterizing the probe state consisting of an even number of photons. We find the optimal measurement attaining the ultimate precision for both parameters in a single setup and perform an experiment based on a pair of photons with an unknown degree of indistinguishability entering a two-port interferometer.
Abstract Two-photon excitation spectroscopy is a nonlinear technique that has gained rapidly in interest and significance for studying the complex energy-level structure and transition probabilities of materials. While the conventional spectroscopy based on tunable classical light has been long established, quantum light provides an alternative way towards excitation spectroscopy with potential advantages in temporal and spectral resolution, as well as reduced photon fluxes. By using a quantum Fourier transform that connects the sum-frequency intensity and N00N-state temporal interference, we present an approach for quantum interferometric two-photon excitation spectroscopy. Our proposed protocol overcomes the difficulties of engineering two-photon joint spectral intensities and fine-tuned absorption-frequency selection. These results may significantly facilitate the use of quantum interferometric spectroscopy for extracting the information about the electronic structure of the two-photon excited-state manifold of atoms or molecules without any requirement for precise and complicated scanning in the spectral domain. This may be particularly relevant for photon-sensitive biological and chemical samples.
Two-photon interference is a cornerstone of quantum optics, enabling imaging, sensing, and precision measurements that surpass classical limits. By harnessing the quantum interference of photon pairs, as demonstrated by the Hong-Ou-Mandel effect, this approach offers superior axial resolution and intrinsic dispersion cancellation, along with strong noise suppression arising from the precise temporal correlations between photons. Building on these principles, we present the theoretical framework and experimental realization of phase-dependent quantum optical coherence tomography (QOCT), a technique that employs phase-modulated two-photon interference for noninvasive morphological analysis of multilayered samples. We demonstrate that introducing controlled phase shifts to photon pairs in a Hong-Ou-Mandel interferometer effectively eliminates artifacts caused by reflections at different sample layers, thereby greatly improving the accuracy and reliability of QOCT measurements. This work advances the fundamental understanding and practical deployment of two-photon interference, overcoming a key limitation in applying QOCT to real-world applications such as biomedical imaging and materials characterization.
Quantum metrology is a subfield of quantum information science that seeks to enhance measurement precision by exploiting quantum phenomena. This thesis presents three experimental investigations that are related to quantum metrology.The first experiment demonstrates a quantum-inspired sub-Rayleigh parameter estimation technique capable of resolving the separation and relative intensities of two incoherent light sources, positioned closer than the Rayleigh criterion. The method relies solely on passive linear optical components, making it readily implementable in standard optical laboratories without specialized equipment. The second experiment demonstrates a scalable protocol for compressing the quantum Fisher information of an arbitrarily large ensemble of identical quantum states into a single quantum state. As a proof of concept, we implement its simplest building block by compressing the quantum Fisher information contained in two qubits into a single qubit. The third experiment demonstrates that entangled probes can optimally estimate the strength of a dephasing channel, including the case where the dephasing axis is unknown.Together, these experiments provide examples of the capabilities of quantum metrology and offer new implementation ideas.
Entangled photon pairs have been used for molecular spectroscopy in the form of entangled two-photon absorption and in quantum interferometry for precise measurements of light source properties and time delays. We present an experiment that combines molecular spectroscopy and quantum interferometry by utilizing the correlations of entangled photons in a Hong-Ou-Mandel (HOM) interferometer to study molecular properties. We find that the HOM signal is sensitive to the presence of a resonant organic sample placed in one arm of the interferometer, and the resulting signal contains information pertaining to the light-matter interaction. We can extract the dephasing time of the coherent response induced by the excitation on a femtosecond time scale. A dephasing time of 102 fs is obtained, which is relatively short compared to times found with similar methods and considering line width broadening and the instrument entanglement time As the measurement is done with coincidence counts as opposed to simply intensity, it is unaffected by even-order dispersion effects, and because interactions with the molecular state affect the photon correlation, the observed measurement contains only these effects and no other classical losses. The experiments are accompanied by theory that predicts the observed temporal shift and captures the entangled photon joint spectral amplitude and the molecule's transmission in the coincidence counting rate. Thus, we present a proof-of-concept experimental method based of entangled photon interferometry that can be used to characterize optical properties in organic molecules and can in the future be expanded on for more complex spectroscopic studies of nonlinear optical properties.