A common challenge in quantum information processing with photons is the limited ability to manipulate and measure correlated states. An example is the inability to measure picosecond-scale temporal correlations of a multiphoton state, given state-of-the-art detectors have a temporal resolution of about 100 ps. Here, we demonstrate temporal magnification of time-bin-entangled two-photon states using a time lens and measure their temporal correlation function, which is otherwise not accessible because of the limited temporal resolution of single-photon detectors. Furthermore, we show that the time lens maps temporal correlations of photons to frequency correlations and could be used to manipulate frequency-bin-entangled photons. This demonstration opens a new avenue to manipulate and analyze spectral and temporal wave functions of many-photon states.
A common challenge in quantum information processing with photons is the limited ability to manipulate and measure correlated states. An example is the inability to measure picosecond-scale temporal correlations of a multiphoton state, given state-of-the-art detectors have a temporal resolution of about 100 ps. Here, we demonstrate temporal magnification of time-bin-entangled two-photon states using a time lens and measure their temporal correlation function, which is otherwise not accessible because of the limited temporal resolution of single-photon detectors. Furthermore, we show that the time lens maps temporal correlations of photons to frequency correlations and could be used to manipulate frequency-bin-entangled photons. This demonstration opens a new avenue to manipulate and analyze spectral and temporal wave functions of many-photon states.
Techniques to control the spectro-temporal properties of quantum states of light at ultrafast time scales are crucial for numerous applications in quantum information science. In this work, we report an all-optical time lens for quantum signals based on Bragg-scattering four-wave mixing with picosecond resolution. Our system achieves a temporal magnification factor of 158 with single-photon level inputs, which is sufficient to overcome the intrinsic timing jitter of superconducting nanowire single-photon detectors. We demonstrate discrimination of two terahertz-bandwidth, single-photon-level pulses with 2.1 ps resolution (electronic jitter corrected resolution of 1.25 ps). We draw on elegant tools from Fourier optics to further show that the time-lens framework can be extended to perform complex unitary spectro-temporal transformations by imparting optimized temporal and spectral phase profiles to the input waveforms. Using numerical optimization techniques, we show that a four-stage transformation can realize an efficient temporal mode sorter that demultiplexes 10 Hermite–Gaussian (HG) modes. Our time-lens-based framework represents a new toolkit for arbitrary spectro-temporal processing of single photons, with applications in temporal mode quantum processing, high-dimensional quantum key distribution, temporal mode matching for quantum networks, and quantum-enhanced sensing with time-frequency entangled states.
Time-frequency entangled photons ("biphotons") exhibit joint spectral and temporal correlations that are unattainable with classical light. Besides being deployed for tests of quantum nonlocality, these photonic states are desirable for a unique range of applications that can significantly impact communications and computation. In this dissertation, we describe novel schemes based on spectral and temporal domain processing for manipulating and characterizing broadband biphotons. Implementing frequency-dependent filters, first, we present and demonstrate a technique for controlling the relative delay between a pair of entangled photons, relying on pump frequency tuning and the quantum concept of nonlocal dispersion cancellation. Next, we demonstrate near-field frequency-to-time mapping, a technique adopted from classical photonics, for arbitrary control of biphoton temporal correlations. Subsequently, we generate temporal correlation trains by creating biphoton frequency combs through programmable spectral amplitude shaping and demonstrate the temporal Talbot effect with entangled photons for the first time. Moreover, in the absence of fast single-photon detectors, we show how electro-optic phase modulation (originally a time-dependent operation) can be used to examine the coherence of biphoton frequency combs. Lastly, we introduce a scheme based on electro-optic intensity modulation, another time-domain operation, for improving the resolution in biphoton temporal correlation measurements. Overall, our body of work could provide additional insight into the manipulation and characterization of biphoton states, as well as contribute towards the improvement of quantum technologies.
A time lens, which can be used to reshape the spectral and temporal properties of light, requires the ultrafast manipulation of optical signals and presents a significant challenge for single-photon application. In this work, we construct a time lens based on dispersion and sum-frequency generation to spectrally engineer single photons from an entangled pair. The strong frequency anticorrelations between photons produced from spontaneous parametric down-conversion are converted to positive correlations after the time lens, consistent with a negative-magnification system. The temporal imaging of single photons enables new techniques for time-frequency quantum state engineering.
Single photons provide a natural platform for quantum communication and quantum networking, as they can be entangled in many degrees of freedom and maintain coherence over long-distance links. However, while their minimal interactions with the environment isolate them from detrimental noise, it can make them difficult to measure and manipulate. In particular, manipulation on the ultrafast timescale is necessary to fully exploit the energy-time (or spectral) photonic degree of freedom. Full control over the spectral properties of single photons is key to many quantum technologies and opens the door to natural high-dimensional quantum encodings. \n \nIn this thesis, we theoretically and experimentally examine the use of nonlinear optical processes mediated by strong laser pulses as a method to control the spectral properties of ultrafast single photons. By mixing single-photon pulses with strong escort pulses that have been shaped through dispersion in a nonlinear crystal, the shape of the escort is imprinted on the photon, resulting in a custom-tailored upconverted pulse. We theoretically examine this process for quadratic spectral phases and show that it has the potential to be simultaneously effective and efficient for the customization of single-photon spectral waveforms, and can be performed in an entanglement-conserving manner. \n \nWe then experimentally demonstrate the range of this technique through three applications. First, we show that sum-frequency generation with shaped pulses can be used to coherently measure time-bin encoded photons with bin separations on the order of picoseconds, well below the timing resolution of our detectors. Secondly, we show that this technique can be adapted to convert a train of pulses to a frequency comb, which can be read out in a straightforward manner using diffraction-based spectrometry. We also show here that this process can be performed in a polarization-maintaining fashion, and demonstrate that entanglement with a partner photon is conserved with high fidelity. Finally, we show that this process can be viewed as a time lens, which modulates a temporal waveform in an analogous fashion to a lens focusing a beam of light. We apply the time lens to a photon from an energy-time entangled pair, and show negative magnification of the joint spectrum through a reversal of the spectral correlations. Such processes could find application in quantum state engineering and high-speed single-photon measurement.
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.