Luis Ledezma’s research while affiliated with California Institute of Technology and other places

Squeezed vacuum, a fundamental resource for continuous-variable quantum information processing, has been used to demonstrate quantum advantages in sensing, communication, and computation. While most experiments use homodyne detection to characterize squeezing and are therefore limited to electronic bandwidths, recent experiments have shown optical parametric amplification (OPA) to be a viable measurement strategy. Here, we realize OPA-based quantum state tomography in integrated photonics and demonstrate the generation and all-optical Wigner tomography of squeezed vacuum in a nanophotonic circuit. We employ dispersion engineering to enable the distortion-free propagation of femtosecond pulses and achieve ultrabroad operation bandwidths, effectively lifting the speed restrictions imposed by traditional electronics on quantum measurements with a theoretical maximum clock speed of 6.5 THz. We implement our circuit on thin-film lithium niobate, a platform compatible with a wide variety of active and passive photonic components. Our results chart a course for realizing all-optical ultrafast quantum information processing in an integrated room-temperature platform.

Few- and single-cycle optical pulses and their associated ultra-broadband spectra have been crucial in the progress of ultrafast science and technology. Multi-color waveforms composed of independently manipulable ultrashort pulses in distinct spectral bands offer unique advantages in pulse synthesis and high harmonic generation. However, the generation and control of ultrashort pulses has required bulky optical systems at the tabletop scale. Quadratic soliton compression theoretically offers a direct route to generation of few-cycle, two-color pulses but is fundamentally limited in bulk systems by the unavoidable presence of walk-off between the fundamental and second harmonic waves. Here, we show that the dispersion engineering capabilities of nanophotonics allow these limitations to be overcome, enabling extreme simultaneous pulse compression of the fundamental and second harmonic components and control over the resultant pulse shape. We experimentally demonstrate quadratic soliton pulse compression in dispersion-engineered nanophotonic lithium niobate waveguides and achieve two-optical-cycle pulses requiring pJ pump pulse energies. We further illustrate how the demonstrated compression scheme can be readily extended to on-chip single-cycle pulse synthesis. When integrated with femtosecond and picosecond sources in lithium niobate, our results provide a path towards realization of single-cycle ultrafast systems in nanophotonic circuits.

Integrated photonic quantum information processing (QIP) has advanced rapidly due to progress in various nanophotonic platforms. Single photon detectors have been the subject of intense study due to their ubiquity in QIP systems, yet many state-of-the art detectors operate at cryogenic temperatures under vacuum and suffer from long dead times. We propose and demonstrate a single photon detection scheme based on optical parametric amplification in nanophotonic lithium niobate (LN) combined with a classical photodetector. We use quantum detector tomography and experimentally demonstrate an efficiency of 26.5% with a 2.2% dark count rate. We show that by improving the nonlinearity-to-loss ratio in nanophotonics and using homodyne detection on a squeezed pump, the detector can achieve 69% efficiency with 0.9% dark count rate. The detector operates at room temperature, has no intrinsic dead time, and is readily integrated in LN nanophotonics, in which many other components of photonic QIP are available. Our results represent a step towards all-optical ultrafast photon detection for scalable nanophotonic QIP.

Optical solitons have long been of interest both from a fundamental perspective and because of their application potential. Both cubic (Kerr) and quadratic nonlinearities can lead to soliton formation, but quadratic solitons can practically benefit from stronger nonlinearity and achieve substantial wavelength conversion. However, despite their rich physics, quadratic cavity solitons have been used only for broadband frequency comb generation, especially in the mid-infrared. Here, we show that the formation dynamics of mid-infrared quadratic cavity solitons, specifically temporal simultons in optical parametric oscillators, can be effectively leveraged to enhance molecular sensing. We demonstrate significant sensitivity enhancement while circumventing constraints of traditional cavity enhancement mechanisms. We perform experiments sensing CO2 using cavity simultons around 4 μm and achieve an enhancement of 6000. Additionally, we demonstrate large sensitivity at high concentrations of CO2, beyond what can be achieved using an equivalent high-finesse linear cavity by orders of magnitude. Our results highlight a path for utilizing quadratic cavity nonlinear dynamics and solitons for molecular sensing beyond what can be achieved using linear methods.

Photonics offers unique capabilities for quantum information processing (QIP) such as room-temperature operation, the scalability of nanophotonics, and access to ultrabroad bandwidths and consequently ultrafast operation. Ultrashort pulse sources of quantum states in nanophotonics are an important building block for achieving scalable ultrafast QIP; however, their demonstrations so far have been sparse. Here, we demonstrate a femtosecond biphoton source in dispersion-engineered periodically poled lithium niobate nanophotonics. We measure 17 THz of bandwidth for the source centered at 2.09 µm, corresponding to a few optical cycles, with a brightness of 8.8 GHz/mW. Our results open new paths toward realization of ultrafast nanophotonic QIP.

Arrays of nonlinear resonators offer a fertile ground for a wide range of complex phenomena and opportunities for advanced photonic sensing and computing. Recently, significant attention has focused on studying coupled resonators in special-purpose configurations either on chips or in table-top experiments. However, a path to realizing a large-scale programmable network of nonlinear photonic resonators remains elusive because of the challenges associated with simultaneously achieving strong nonlinearity, independent operation of the resonators, and programmability of the couplings. In this work, we break these barriers by realizing large-scale, time-multiplexed optical parametric oscillators (OPOs) on a single lithium niobate nanophotonic chip. We show independent operation of 70 identical OPOs in an ultrafast nanophotonic circuit. The OPOs exhibit an ultra-low threshold of a few picojoules, substantially surpassing the strength of nonlinearity of other platforms. Using our ultrafast nanophotonic circuit, a network of N OPOs with programmable all-to-all couplings requires only a few additional components. The time-multiplexed nanophotonic OPOs can enable myriad applications, including ultrafast classical and quantum information processing.

Traditional absorption spectroscopy has a fundamental difficulty in resolving small absorbance from a strong background due to the instability of laser sources. Existing background-free methods in broadband vibrational spectroscopy help to alleviate this problem but face challenges in realizing either low extinction ratios or time-resolved field measurements. Here, we introduce optical-parametric-amplification-enhanced background-free spectroscopy, in which the excitation background is first suppressed by an interferometer, and then the free-induction decay that carries molecular signatures is selectively amplified. We show that this method can improve the limit of detection in linear interferometry by order(s) of magnitude without requiring lower extinction ratios or a time-resolved measurement, which can benefit sensing applications in detecting trace species.

Efficient on-chip entangled photon pair generation at telecom wavelengths is an integral aspect of emerging quantum optical technologies, particularly for quantum communication and computing. However, moving to shorter wavelengths enables the use of more accessible silicon detector technology, and opens up applications in imaging and spectroscopy. Here, we present high brightness ((1.6 ± 0.3) × 10⁹ pairs/s/mW/nm) visible–near-IR photon pair generation in a periodically poled lithium niobate nanophotonic waveguide. The degenerate spectrum of the photon pairs is centered at 811 nm with a bandwidth of 117 nm when pumped with a spectrally multimode laser diode. The measured on-chip source efficiency of (2.3 ± 0.5) × 10¹¹ pairs/s/mW is on par with source efficiencies at telecom wavelengths and is also orders of magnitude higher than the efficiencies of other visible sources implemented in bulk crystal or diffused waveguide-based technologies. Further improvements in the brightness and efficiencies are possible by pumping the device with a single-frequency laser, which would also shrink the pair bandwidth. These results represent the shortest wavelength of photon pairs generated in a nanophotonic waveguide reported to date by nearly an octave.