Abstract We demonstrated an ultrafast time-resolved measurement method operating at the single-photon level and employing a two-color comb-based asynchronous optical sampling (ASOPS) setup. We harnessed the two-color ASOPS photon counting approach to achieve long-term averaging of the ultralow intensity signal with a synchronized optical trigger signal, which minimizes residual timing jitter between the two combs. A pulse-width limited picosecond cross-correlation signal was successfully obtained with a power level of <1 photon/pulse. This approach enables the thorough study of ultrafast time-resolved detection of entangled photon pairs, quantum mechanical correlations in the time-frequency domain and finds wide use in optical quantum technology.
Abstract We demonstrated an ultrafast time-resolved measurement method operating at the single-photon level and employing a two-color comb-based asynchronous optical sampling (ASOPS) setup. We harnessed the two-color ASOPS photon counting approach to achieve long-term averaging of the ultralow intensity signal with a synchronized optical trigger signal, which minimizes residual timing jitter between the two combs. A pulse-width limited picosecond cross-correlation signal was successfully obtained with a power level of <1 photon/pulse. This approach enables the thorough study of ultrafast time-resolved detection of entangled photon pairs, quantum mechanical correlations in the time-frequency domain and finds wide use in optical quantum technology.
The nonclassical light sources, such as frequency-time entangled photons, are anticipated to offer significant benefits for emerging quantum optical sensing or spectroscopic measurements and manifest on ultrafast time scales (sub-ps to fs). However, the constrained time resolution (ns to ps) of photon-counting detectors poses challenges in comprehensively characterizing their detailed properties on ultrafast time scales. Therefore, we present a novel asynchronous optical sampling (ASOPS) technique utilizing two-color optical frequency combs to demonstrate highly precise and sensitive ultrafast time-resolved cross-correlation measurements at the single-photon level. By employing photon counting statistics, this method successfully reconstructed the picosecond pulse width cross-correlation waveforms at extremely low power level (<1 photon per pulse), while effectively suppressing the residual temporal jitter between the two combs via optically triggered averaging using asynchronous optical sampling of combs. The use of repetition frequency stabilized distinct-wavelength pulses allowed for the effective suppression of strong background light from the pump through spectral filtering, achieving single-photon sensitivity. Subsequently, we parametrically down converted the frequency doubled light from the Er comb in the nonlinear ppKTP waveguide to generate quantum entangled photons at telecom band. A 9.04% Klyshko efficiency with a photon pair generation rate of 0.98 MHz/mW was obtained using heralding detection. Employing the established ASOPS technique to the generated photon pairs enabled the realization of ultrafast time-resolved and quantum mechanical correlation measurements. This paves the way for a versatile and comprehensive manipulation of quantum-entangled photon pairs in the time-domain, with potential applications in ultrafast optical quantum technology and ultrashort fluorescence measurements.
Quantum correlations of ultrafast quantum optical states in the time–frequency domain manifest prominently on femtosecond time scales, an elusive challenging regime. We develop a new method to probe the time–frequency mode structure of ultrafast two-photon states utilizing dual-comb-based asynchronously overlapping pulses with single-photon frequency upconversion through femtosecond optical sampling. This method enables quick, highly precise joint temporal intensity measurements over a broad temporal dynamic range with only a single linear scanning stage. We demonstrate full characterization of time–frequency entangled two-photon states in both time and frequency domains. We quantified the time–frequency mode structure in both time and frequency domains through Schmidt decomposition, resulting in temporal and spectral purities of 87.7% and 76.9%, respectively, for heralded single-photons without any spectral filtering. Furthermore, through the simple control of pump spectral bandwidth, we demonstrate the ability to tailor time–frequency entanglement, verifying the two-dimensional Fourier duality. This method paves the way for a substantial upgrade to ultrafast quantum optical techniques, enabling a rapid, detailed, and multi-dimensional characterization of entangled states with potential applications in quantum metrology and photon-deficient fluorescence imaging.
Classical time-resolved optical spectroscopy experiments are performed using sequences of ultrashort light pulses, with photon fluxes incident on the sample which are many orders of magnitude higher than real-world conditions corresponding to sunlight illumination. Here we overcome this paradigm by exploiting quantum correlations to perform time-resolved spectroscopy with entangled photons. Starting from spontaneous parametric down-conversion driven by a continuous-wave laser, we exploit the temporal entanglement between randomly generated signal/idler pairs to obtain temporal resolution, and their spectral entanglement to select the excitation frequency. We also add spectral resolution in detection, using a Fourier transform approach which employs a common-path interferometer. We demonstrate the potential of our entangled-photon streak camera by resolving, at the single-photon level, excitation energy transfer cascades from LH2 to LH1 in the photosynthetic membrane and disentangling the lifetimes of two dyes in a mixture. We show that time-resolved spectroscopy with quantum light can be performed without compromising measurement time, recording a fluorescence time trace in less than a minute even for samples with low quantum yield, which can be reduced to sub-second times with acceptable signal-to-noise ratio. Our results provide a new approach to ultrafast optical spectroscopy, where experiments are performed under conditions comparable to real-world sunlight illumination.
Classical time-resolved optical spectroscopy experiments are performed using sequences of ultrashort light pulses, with photon fluxes incident on the sample which are many orders of magnitude higher than real-world conditions corresponding to sunlight illumination. Spectroscopy and microscopy schemes that use quantum states of light have been widely described theoretically with fewer experimental demonstrations that typically require very long measurements that can extend for hours or more. Here, we show that time-resolved spectroscopy with quantum light can be performed without compromising measurement time or wavelength tunability, recording a fluorescence lifetime trace in biological samples in less than a second with acceptable signal-to-noise ratio. Starting from spontaneous parametric down-conversion driven by a continuous-wave laser, we exploit the temporal correlation between randomly generated signal/idler pairs to obtain temporal resolution, and their spectral correlation to select the excitation frequency. We also add spectral resolution in detection, using a 'photon-efficient' Fourier transform approach which employs a common-path interferometer. We demonstrate the potential of this approach by resolving, at the single-photon level, excitation energy transfer cascades from LH2 to LH1 in the photosynthetic membrane and disentangling the lifetimes of two dyes in a mixture. Our results provide a new approach to ultrafast optical spectroscopy, where experiments are performed under illumination intensity conditions comparable to real-world sunlight illumination.
Single photons are a natural platform for quantum technologies as they support entanglement in many degrees of freedom and are inherently well protected from a detrimental type of noise called decoherence. In order to fully exploit photons for quantum technologies, it will be necessary to be able to shape, control, and measure their properties in all degrees of freedom: space, time, frequency, and polarization. \n \n The time-frequency degree of freedom of light is of particular interest for quantum information tasks as it supports various encodings, including frequency bins and time bins, and is intrinsically robust for propagation through long-distance fibre links. Applications which harness quantum correlations in this degree of freedom, referred to as energy-time entanglement, include dispersion cancellation and high-dimensional quantum key distribution. However, detection of this entanglement and observation of these effects requires time resolution beyond the capabilities of current photon detectors. Thus, for operations on ultrafast time scales, more powerful and complex methods are required. \n \n In this thesis, we use a nonlinear technique known as optical gating to surpass the limitations in current detectors and measure single photon pairs, improving the time resolution by two orders of magnitude. When a single photon enters a nonlinear medium at the same time as a strong laser pulse, it may upconvert to a higher energy photon. The strong laser pulse effectively acts as an ultrafast shutter or gate and this creates a high resolution snapshot of the photon in time. Optical gating in conjunction with single photon spectrometers then allow us to measure both the spectral and temporal features of photons on subpicosecond time scales. \n \n These high resolution measurements enable us to explore a host of quantum effects which remained previously inaccessible. First, we directly observe energy-time entanglement, analogous to Einstein-Rosen-Podolsky correlations but \\emph{in frequency and time}. Then, with full control over the dispersion of each photon, we observe nonlocal dispersion cancellation on femtosecond time scales. We also explore ultrafast interferometry in the quantum domain by temporally resolving two-photon interference from a Franson interferometer and observe a violation of the CHSH-Bell inequality. Finally, we show that, using these measurements, it is possible to reconstruct a two-photon energy-time entangled state. Such measurement capabilities will be essential to precisely control both the spectral and temporal shape of entangled photons and to develop new applications in quantum state engineering.