Subscribe to the gold package and get unlimited access to Shamra Academy
Register a new userAchieving two-dimensional optical spectroscopy with temporal and spectral resolution using quantum entangled three photons
214
0
0.0
(
0
)
Ask ChatGPT about the research
No Arabic abstract
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 spectroscopic measurement utilizing entangled three photons. In this measurement, time-resolved entangled photon spectroscopy with monochromatic pumping [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.
rate research
Read More
We present single- and multiple-quantum correlation $J$-spectroscopy detected in zero ($<!!1$~$mu$G) magnetic field using a Rb vapor-cell magnetometer. At zero field the spectrum of ethanol appears as a mixture of carbon isotopomers, and correlation spectroscopy is useful in separating the two composite spectra. We also identify and observe the zero-field equivalent of a double-quantum transition in ${}^{13}$C$_2$-acetic acid, and show that such transitions are of use in spectral assignment. Two-dimensional spectroscopy further improves the high resolution attained in zero-field NMR since selection rules on the coherence-transfer pathways allow for the separation of otherwise overlapping resonances into distinct cross-peaks.
A quantum dot can be used as a source of one- and two-photon states and of polarisation entangled photon pairs. The emission of such states is investigated from the point of view of frequency-resolved two-photon correlations. These follow from a spectral filtering of the dot emission, which can be achieved either by using a cavity or by placing a number of interference filters before the detectors. The combination of these various options is used to iteratively refine the emission in a distillation process and arrive at highly correlated states with a high purity. So-called leapfrog processes where the system undergoes a direct transition from the biexciton state to the ground state by direct emission of two photons, are shown to be central to the quantum features of such sources. Optimum configurations are singled out in a global theoretical picture that unifies the various regimes of operation.
Graph representations are a powerful concept for solving complex problems across natural science, as patterns of connectivity can give rise to a multitude of emergent phenomena. Graph-based approaches have proven particularly fruitful in quantum communication and quantum search algorithms in highly branched quantum networks. Here we introduce a new paradigm for the direct experimental realization of excitation dynamics associated with three-dimensional networks by exploiting the hybrid action of spatial and polarization degrees of freedom of photon pairs in complex waveguide circuits with tailored birefringence. This novel testbed for the experimental exploration of multi-particle quantum walks on complex, highly connected graphs paves the way towards exploiting the applicative potential of fermionic dynamics in integrated quantum photonics.
Optical interferometry has been a long-standing setup for characterization of quantum states of light. Both the linear and the nonlinear interferences can provide information about the light statistics an 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.
Two-photon excitation (TPE) proceeds via a virtual pathway, which depends on the accessibility of one or more intermediate states, and, in the case of non-centrosymmetric molecules, an additional dipole pathway involving the off-resonance dipole-allowed one-photon transitions and the change in the permanent dipole moment between the initial and final states. Here, we control the quantum interference between these two optical excitation pathways by using phase-shaped femtosecond laser pulses. We find enhancements by a factor of up to 1.75 in the two-photon-excited fluorescence of the photobase FR0-SB in methanol after taking into account the longer pulse duration of the shaped laser pulses. Simulations taking into account the different responses of the virtual and dipole pathways to external fields and the effect of pulse shaping on two-photon transitions are found to be in good agreement with our experimental measurements. The observed quantum control of TPE in condensed phase may lead to enhanced signal at a lower intensity in two-photon microscopy, multiphoton-excited photoreagents, and novel spectroscopic techniques that are sensitive to the magnitude of the contributions from the virtual and dipole pathways to multiphoton excitations.
Log in to be able to interact and post comments
comments
Fetching comments
Sign in to be able to follow your search criteria
