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Register a new userPhase shift-cavity ring down spectroscopy in linear and active fiber cavities for sensing applications at 1550 nm
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Liquid phase sensing applications at 1550~nm are highly desirable due to widely available off-the-shelf components. Generally, liquids at 1550~nm induce a high absorption loss that limits the overall sensors sensitivity and detection limit. One solution is to use an active fiber loop in conjunction with cavity ring down spectroscopy to overcome these absorption losses. However, the amplifier inside the fiber loop suffers from inherent gain fluctuations that limit the sensing systems overall performance. Here, we provide a novel sensor using the wavelength-scanned phase shift-cavity ring down spectroscopy (PS-CRDS) in conjunction with a linear active fiber cavity that potentially offers a more sensitive solution than traditional fiber loop sensors. We use a tapered fiber as a sensing head inside the active cavity built from fiber Bragg gratings. We derive a theoretical phase shift expression for our system and simulate it using the finite element method to determine optimum tapered fiber diameter for glucose sensing in DI water. Compared to a non-amplified system, we find that our amplified system can increase the sensitivity by fourteen times via the amplifier gain tuning. We also conduct experimental measurements using 0-15.5~mM glucose solutions and find them in excellent agreement with our theoretical predictions. Experimentally we obtain the sensors sensitivity of 0.768~$^o$/mM (1164~$^o$/RIU) and detection limit of 0.75~mM ( 4.5~$times$~10$^{-4}$~RIU) without any temperature stabilization in the system. We anticipate that the present work will find a wide range of sensing applications in fiber cavities, ring resonators, and other microcavity structures.
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Cavity ring-down spectroscopy is a ubiquitous optical method used to study light-matter interactions with high resolution, sensitivity and accuracy. However, it has never been performed with the multiplexing advantages of direct frequency comb spectroscopy without sacrificing orders of magnitude of resolution. We present dual-comb cavity ring-down spectroscopy (DC-CRDS) based on the parallel heterodyne detection of ring-down signals with a local oscillator comb to yield absorption and dispersion spectra. These spectra are obtained from widths and positions of cavity modes. We present two approaches which leverage the dynamic cavity response to coherently or randomly driven changes in the amplitude or frequency of the probe field. Both techniques yield accurate spectra of methane - an important greenhouse gas and breath biomarker. The high sensitivity and accuracy of broadband DC-CRDS, shows promise for applications like studies of the structure and dynamics of large molecules, multispecies trace gas detection and isotopic composition.
Optical resonant microcavities with ultra high quality factors are widely used for biosensing. Until now, the primary method of detection has been based upon tracking the resonant wavelength shift as a function of biodetection events. One of the sources of noise in all resonant-wavelength shift measurements is the noise due to intensity fluctuations of the laser source. An alternative approach is to track the change in the quality factor of the optical cavity by using phase shift cavity ring down spectroscopy, a technique which is insensitive to the intensity fluctuations of the laser source. Here, using biotinylated microtoroid resonant cavities, we show simultaneous measurement of the quality factor and the wavelength shift by using phase shift cavity ring down spectroscopy. These measurements were performed for disassociation phase of biotin-streptavidin reaction. We found that the disassociation curves are in good agreement with the previously published results. Hence, we demonstrate not only the application of phase shift cavity ring down spectroscopy to microcavities in the liquid phase but also simultaneous measurement of the quality factor and the wavelength shift for the microcavity biosensors in the application of kinetics measurements.
Aflatoxin M1 (AFM1) is a carcinogenic compound commonly found in milk in excess of the WHO permissible limit, especially in developing countries. Currently, state-of-the-art tests for detecting AFM1 in milk include chromatographic systems and enzyme-linked-immunosorbent assays. Although these tests provide fair accuracy and sensitivity however, they require trained laboratory personnel, expensive infrastructure, and many hours for producing final results. Optical sensors leveraging spectroscopy have a tremendous potential of providing an accurate, real time, and specialists-free AFM1 detector. Despite this, AFM1 sensing demonstrations using optical spectroscopy are still immature. Here, we demonstrate an optical sensor that employs the principle of cavity attenuated phase shift spectroscopy in optical fiber cavities for rapid AFM1 detection in aqueous solutions at 1550 nm. The sensor constitutes a cavity built by two fiber Bragg gratings. We splice a tapered fiber of $<$ 10 $mu$m waist inside the cavity as a sensing head. For ensuring specific binding of AFM1 in a solution, the tapered fiber is functionalized with DNA aptamers followed by validation of the conjugation via FTIR, TGA, and EDX analyses. We then detect AFM1 in a solution by measuring the phase shift between a sinusoidally modulated laser input and the sensor output at resonant frequencies of the cavity. Our results show that the sensor has the detection limit of 20 ng/L (20 ppt) which is well below both the US and the European safety regulations. We anticipate that the present work will lead towards a rapid and accurate AFM1 sensor, especially for low-resource settings.
High coherent frequency-entangled photons at telecom band are critical in quantum information protocols and quantum tele-communication. While photon pairs generated by spontaneous parametric down-conversion in nonlinear crystal or modulation instability in optical fiber exhibit random fluctuations, making the photons distinguishable among consecutive roundtrips. Here, we demonstrate a frequency-entangled photons based on parametric instability in an active fiber ring cavity, where periodic modulation of dispersion excites parametric resonance. The characteristic wave number in parametric instability is selected by the periodic modulation of resonator, and stable patterns with symmetric gains are formed. We find that the spectra of parametric instability sidebands possess a high degree of coherence, which is verified by the background-free autocorrelation of single-shot spectra. Two photon interference is performed by a fiber-based Mach-Zehnder interferometer without any stabilization. We obtain a Hong-Ou-Mandel interference visibility of 86.3% with a dip width of 4.3 mm. The correlation time measurement exhibits a linewidth of 68.36 MHz, indicating high coherence and indistinguishability among the photon pairs. Our results proves that the parametric instability in active fiber cavity is effective to generate high coherent frequency-entangled photon pairs, which would facilitate subsequent quantum applications.
We describe a fiber Raman amplifier for nanosecond and sub-nanosecond pulses centered around 1260 nm. The amplification takes place inside a 4.5-m-long polarization-maintaining phosphorus-doped fiber, pumped at 1080 nm by 3-ns-long pulses with a repetition rate of 200 kHz and up to 1.75 kW peak power. The input seed pulses are of sub-mW peak-power and minimal duration of 0.25 ns, carved off a continuous-wave laser with sub-MHz linewidth. We obtain linearly-polarized output pulses with peak-powers of up to 1.4 kW, corresponding to peak-power conversion efficiency of over 80%. An ultrahigh small-signal-gain of 90 dB is achieved, and the signal-to-noise ratio 3 dB below the saturation power is above 20 dB. No significant temporal and spectral broadening is observed for output pulses up to 400 W peak power, and broadening at higher powers can be reduced by phase modulation of the seed pulse. Thus nearly-transform-limited pulses with peak power up to 1 kW are obtained. Finally, we demonstrate the generation of pulses with controllable frequency chirp, pulses with variable width, and double pulses. This amplifier is thus suitable for coherent control of narrow atomic resonances and especially for the fast and coherent excitation of rubidium atoms to Rydberg states. These abilities open the way towards several important applications in quantum non-linear optics.
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