The true role of entanglement in two-photon virtual-state spectroscopy (Saleh et al 1998 Phys. Rev. Lett. 80 3483), a two-photon absorption spectroscopic technique that can retrieve information about the energy level structure of an atom or a molecule, is controversial. The consideration of closely related techniques, such as multidimensional pump-probe spectroscopy (Roslyak et al 2009 Phys. Rev. A 79, 063409), suggests that spectroscopic information might also be retrieved by using uncorrelated pairs of photons. Here we show that this is not the case. In the two-photon absorption process, the ability to obtain information about the energy level structure of a medium depends on the spectral shape of existing temporal (frequency) correlations between the absorbed photons. In fact, it is a combination of both the presence of frequency correlations (entanglement) and their specific spectral shape that makes the
It has been argued that excitonic energy transport in photosynthetic complexes is efficient because of a balance between coherent evolution and decoherence, a phenomenon called environment-assisted quantum transport (ENAQT). Studies of ENAQT have usually assumed that the excitation is initially localized on a particular chromophore, and that it is transferred to a reaction center through a similarly localized trap. However, these assumptions are not physically accurate. We show that more realistic models of excitation and trapping can lead to very different predictions about the importance of ENAQT. In particular, although ENAQT is a robust effect if one assumes a localized trap, its effect can be negligible if the trapping is more accurately modeled as Förster transfer to a reaction center. Our results call into question the suggested role of ENAQT in the photosynthetic process of green sulfur bacteria and highlight the subtleties associated with drawing lessons for designing biomimetic light-harvesting complexes.
The identification of light sources represents a task of utmost importance for the development of multiple photonic technologies. Over the last decades, the identification of light sources as diverse as sunlight, laser radiation, and molecule fluorescence has relied on the collection of photon statistics or the implementation of quantum state tomography. In general, this task requires an extensive number of measurements to unveil the characteristic statistical fluctuations and correlation properties of light, particularly in the low-photon flux regime. In this article, we exploit the self-learning features of artificial neural networks and the naive Bayes classifier to dramatically reduce the number of measurements required to discriminate thermal light from coherent light at the single-photon level. We demonstrate robust light identification with tens of measurements at mean photon numbers below one. In terms of accuracy and number of measurements, the methods described here dramatically outperform conventional schemes for characterization of light sources. Our work has important implications for multiple photonic technologies such as light detection and ranging, and microscopy.
The quantum theory of electromagnetic radiation predicts characteristic statistical fluctuations for light sources as diverse as sunlight, laser radiation and molecule fluorescence. Indeed, these underlying statistical fluctuations of light are associated with the fundamental physical processes behind their generation. In this contribution, we demonstrate that the manipulation of the quantum electromagnetic fluctuations of a pair of vacuum states leads to a novel family of quantum-correlated multiphoton states with tunable mean photon numbers and degree of correlation. Our technique relies on the use of conditional measurements to engineer the excitation mode of the field through the simultaneous subtraction of photons from two-mode squeezed vacuum states. The experimental generation of multiphoton states with quantum correlations by means of photon subtraction unveils novel mechanisms to control fundamental properties of light. As a remarkable example, we demonstrate the engineering of a quantum correlated state of light, with nearly Poissonian photon statistics, that constitutes the first step towards the generation of entangled lasers. Our technique enables a robust protocol to prepare quantum states with multiple photons in high-dimensional spaces and, as such, it constitutes a novel platform for exploring quantum phenomena in mesoscopic systems.The identification of the photon as a fundamental carrier of information has triggered a wide variety of research that aims to improve the state of the art of photonic technologies [1]. Along these lines, the field of quantum photonics has focused on exploiting the quantum properties of light to dramatically improve the performance of protocols for communication, metrology, imaging, and information processing [2-4]. Consequently, the successful implementation of functional quantum photonic technologies hinges on our ability to generate, manipulate, and measure complex multiphoton states [5][6][7]. However, the generation of high-dimensional entangled states comprising a large number of photons is nowadays one of the most challenging tasks in quantum optics [8,9].Over the past few years, physicists and engineers have demonstrated the utilization of multiple degrees of freedom of single photons to perform information processing tasks for a wide range of applications. In this regard, multiple bits of information have successfully been encoded in a single photon by preparing complex superpositions in time, frequency, position, transverse momentum, angular position, orbital angular momentum and path [10][11][12][13][14][15]. The complexity of such superpositions has led to important improvements in the performance and tolerance of cryptographic protocols, in the estimation of small physical parameters, and in the development of novel schemes for information processing [1][2][3][4]. Furthermore, it is now recognized that such protocols can be further improved by incorporating a high number of pho-tons, correlated and entangled [16][17][18][19]. Interestingly, the generation...
Passive parity-time symmetry breaking transitions, where long-lived eigenmodes emerge in a locally dissipative system, have been extensively studied in recent years. Conventional wisdom says that they occur at exceptional points. Here we report the observation of multiple transitions showing the emergence of slowly decaying eigenmodes in a dissipative, Floquet electronic system with synthetic components. Remarkably, in our system, the modes emerge without exceptional points. Our setup uses an electrical oscillator inductively coupled to a dissipative oscillator, where the time-periodic inductive coupling and resistive-heating losses are independently controlled. With a Floquet dissipation, slowly-decaying eigenmodes emerge at vanishingly small dissipation strength in the weak coupling limit. With a moderate Floquet coupling, multiple instances of their emergence and disappearance are observed. With an asymmetric dimer model, we show that these transitions, driven by avoided-levelcrossing in purely dissipative systems, are generically present in static and Floquet domains.
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.
customersupport@researchsolutions.com
10624 S. Eastern Ave., Ste. A-614
Henderson, NV 89052, USA
This site is protected by reCAPTCHA and the Google Privacy Policy and Terms of Service apply.
Copyright © 2024 scite LLC. All rights reserved.
Made with 💙 for researchers
Part of the Research Solutions Family.