Search Results
Ultrafast laser inscription of asymmetric integrated waveguide 3 dB couplers for astronomical K-band interferometry at the CHARA array
2021, Benoît, Aurélien, Pike, Fraser A., Sharma, Tarun K., MacLachlan, David G., Dinkelaker, Aline N., Nayak, Abani S., Madhav, Kalaga, Roth, Martin M., Labadie, Lucas, Pedretti, Ettore, Brummelaar, Theo A. ten, Scott, Nic, Coudé du Foresto, Vincent, Thomson, Robert R.
We present the fabrication and characterization of 3 dB asymmetric directional couplers for the astronomical K-band at wavelengths between 2.0 and 2.4 µm. The couplers were fabricated in commercial Infrasil silica glass using an ultrafast laser operating at 1030 nm. After optimizing the fabrication parameters, the insertion losses of straight single-mode waveguides were measured to be ∼1.2±0.5dB across the full K-band. We investigate the development of asymmetric 3 dB directional couplers by varying the coupler interaction lengths and by varying the width of one of the waveguide cores to detune the propagation constants of the coupled modes. In this manner, we demonstrate that ultrafast laser inscription is capable of fabricating asymmetric 3 dB directional couplers for future applications in K-band stellar interferometry. Finally, we demonstrate that our couplers exhibit an interferometric fringe contrast of >90%. This technology paves the path for the development of a two-telescope K-band integrated optic beam combiner for interferometry to replace the existing beam combiner (MONA) in Jouvence of the Fiber Linked Unit for Recombination (JouFLU) at the Center for High Angular Resolution Astronomy (CHARA) telescope array.
Observing mode-dependent wavelength-to-time mapping in few-mode fibers using a single-photon detector array
2020, Chandrasekharan, Harikumar K., Ehrlich, Katjana, Tanner, Michael G., Haynes, Dionne M., Mukherjee, Sebabrata, Birks, Tim A., Thomson, Robert R.
Wavelength-to-time mapping (WTM)—stretching ultrashort optical pulses in a dispersive medium such that the instantaneous frequency becomes time-dependent—is usually performed using a single-mode fiber. In a number of applications, such as time-stretch imaging (TSI), the use of this single-mode fiber during WTM limits the achievable sampling rate and the imaging quality. Multimode fiber based WTM is a potential route to overcome this challenge and project a more diverse range of light patterns. Here, we demonstrate the use of a twodimensional single-photon avalanche diode (SPAD) array to image, in a time-correlated single-photon counting (TCSPC) manner, the time- and wavelength-dependent arrival of different spatial modes in a few-mode fiber. We then use a TCSPC spectrometer with a onedimensional SPAD array to record and calibrate the wavelength-dependent and mode-dependent WTM processes. The direct measurement of the WTM of the spatial modes opens a convenient route to estimate group velocity dispersion, differential mode delay, and the effective refractive index of different spatial modes. This is applicable to TSI and ultrafast optical imaging, as well as broader areas such as telecommunications.
High-speed dual color fluorescence lifetime endomicroscopy for highly-multiplexed pulmonary diagnostic applications and detection of labeled bacteria
2019, Pedretti, Ettore, Tanner, Michael G., Choudhary, Tushar R., Krstajic, Nikola, Megia-Fernandez, Alicia, Henderson, Robert K., Bradley, Mark, Thomson, Robert R., Girkin, John M., Dhaliwal, Kevin, Dalgarno, Paul A.
We present a dual-color laser scanning endomicroscope capable of fluorescence lifetime endomicroscopy at one frame per second (FPS). The scanning system uses a coherent imaging fiber with 30,000 cores. High-speed lifetime imaging is achieved by distributing the signal over an array of 1024 parallel single-photon avalanche diode detectors (SPADs), minimizing detection dead-time maximizing the number of photons detected per excitation pulse without photon pile-up to achieve the high frame rate. This also enables dual color fluorescence imaging by temporally shifting the dual excitation lasers, with respect to each other, to separate the two spectrally distinct fluorescent decays in time. Combining the temporal encoding, to provide spectral separation, with lifetime measurements we show a one FPS, multi-channel endomicroscopy platform for clinical applications and diagnosis. We demonstrate the potential of the system by imaging SmartProbe labeled bacteria in ex vivo samples of human lung using lifetimeto differentiate bacterial fluorescence from the strong background lung autofluorescence which was used to provide structural information.