Quantum interferences of entangled photons have engendered tremendous intriguing phenomena that lack any counterpart in classical physics. Hitherto, owing to the salient properties of quantum optics, quantum interference has been widely studied and provides useful tools that ultimately broaden the path towards ultra-sensitive quantum metrology, ranging from sub-shot-noise quantum sensing to high-resolution optical spectroscopy. In particular, quantum interferometric metrology is an essential requisite for extracting information about the structure and dynamics of photon-sensitive biological and chemical molecules. This article reviews the theoretical and experimental progress of this quantum interferometric metrology technology along with their advanced applications. The scope of this review includes Hong–Ou–Mandel interferometry with ultrahigh timing resolution, entanglement-assisted absorption spectroscopy based on a Fourier transform, and virtual-state spectroscopy using tunable energy-time entangled photons.
Quantum interferences of entangled photons have engendered tremendous intriguing phenomena that lack any counterpart in classical physics. Hitherto, owing to the salient properties of quantum optics, quantum interference has been widely studied and provides useful tools that ultimately broaden the path towards ultra-sensitive quantum metrology, ranging from sub-shot-noise quantum sensing to high-resolution optical spectroscopy. In particular, quantum interferometric metrology is an essential requisite for extracting information about the structure and dynamics of photon-sensitive biological and chemical molecules. This article reviews the theoretical and experimental progress of this quantum interferometric metrology technology along with their advanced applications. The scope of this review includes Hong–Ou–Mandel interferometry with ultrahigh timing resolution, entanglement-assisted absorption spectroscopy based on a Fourier transform, and virtual-state spectroscopy using tunable energy-time entangled photons.
Absorption spectroscopy has long been hailed as an absolute necessity for detecting the properties of complex chemical and biological samples. While conventional spectroscopy using classical light is severely limited by shot noise and lacks robustness against experimental imperfections, quantum light offers an avenue to perform absorption spectroscopy with provable advantages in the technical operations and the measurement precision. Here, we present an experimental approach to implement entanglement-based absorption spectroscopy with the assistance of Hong-Ou-Mandel interference. Since the temporal interference fringe is determined by the spectrum pattern, a maximum-likelihood decision is sufficient for revealing the relevant quantum information about the absorptive properties of the test samples. These experimental results may significantly facilitate the use of quantum interferometric spectroscopy to practical applications, which may be particularly relevant for photon-sensitive biological and chemical samples.
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.
Abstract Optical interferometry has been a long-standing setup for characterization of quantum states of light. Both linear and the nonlinear interferences can provide information regarding the light statistics and underlying detail of the light-matter interactions. Here we demonstrate how interferometric detection of nonlinear spectroscopic signals may be used to improve the measurement accuracy of matter susceptibilities. Light-matter interactions change the photon statistics of quantum light, which are encoded in the field correlation functions. Application is made to the Hong-Ou-Mandel two-photon interferometer that reveals entanglement-enhanced resolution that can be achieved with existing optical technology.
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.
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 entanglement, a hallmark of quantum mechanics, offers unprecedented opportunities to revolutionize spectroscopic techniques. This paper explores the theoretical underpinnings and experimental prospects of quantum entanglement-enhanced spectroscopy for the precise probing of coherent dynamics in complex chemical systems. Traditional spectroscopic methods often face limitations in resolution, sensitivity, and the ability to distinguish subtle quantum phenomena due to their reliance on classical light sources. By harnessing entangled photons, it is possible to overcome these limitations, enabling sub-shot-noise measurements, enhanced spectral resolution beyond the diffraction limit, and access to non-classical correlations within molecular systems. We delve into how entangled light can be generated and engineered to interact with molecular ensembles, facilitating the study of processes such as exciton transport, charge transfer, and vibrational energy redistribution with extraordinary fidelity. The methodology section outlines conceptual experimental setups, including entangled two-photon absorption spectroscopy and quantum Ramsey interferometry, discussing the benefits of these approaches over their classical counterparts. We present hypothetical results demonstrating how entanglement can resolve overlapping spectral features, extend coherence lifetimes, and provide unique insights into the quantum pathways governing chemical reactions. The discussion addresses the challenges associated with maintaining entanglement in noisy chemical environments and outlines strategies for mitigating decoherence. Ultimately, entanglement-enhanced spectroscopy represents a transformative paradigm for chemical physics, promising a deeper understanding of fundamental quantum processes that dictate reactivity and function in biological and material sciences.