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Journal of Applied Physics

Delayed optical nutation inside a hollow-core photonic crystal fiber filled with acetylene

Manuel Ocegueda, Serguei I. Stepanov, Jordan Diaz, Nayeli Casillas, Eliseo Hernández, Priscilla E. Iglesias

Published Jun 22, 2020• 3 citations
Publisher

Abstract

The delayed optical nutation effect has been used to evaluate the longitudinal relaxation time (T1) inside an acetylene-filled hollow-core photonic crystal fiber (HC-PCF) at room temperature. In this experiment, sequences of two short optical pulses of 30 ns and 15 ns in width, respectively, with the maximum peak power up to ∼2.5 W, were generated at a laser wavelength of 1530.37 nm, which corresponds to the acetylene ro-vibrational P9 absorption line. The gas pressure inside the 1 m-long HC-PCF varied in the range 0.1–1 Torr. Numerical simulations based on the optical Bloch equations allowed us to evaluate the longitudinal relaxation time as T1∼9ns, proving to be fundamentally limited by the transit-time broadening. Also, the obtained results revealed the influence of slow and fast molecules in the form of a non-exponential decay of the delayed-nutation signals.

DOI
10.1063/5.0006931

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The delayed optical nutation effect has been used to evaluate the longitudinal relaxation time (T1) inside an acetylene-filled hollow-core photonic crystal fiber (HC-PCF) at room temperature. In this experiment, sequences of two short optical pulses of 30 ns and 15 ns in width, respectively, with the maximum peak power up to ∼2.5 W, were generated at a laser wavelength of 1530.37 nm, which corresponds to the acetylene ro-vibrational P9 absorption line. The gas pressure inside the 1 m-long HC-PCF varied in the range 0.1–1 Torr. Numerical simulations based on the optical Bloch equations allowed us to evaluate the longitudinal relaxation time as T1∼9ns, proving to be fundamentally limited by the transit-time broadening. Also, the obtained results revealed the influence of slow and fast molecules in the form of a non-exponential decay of the delayed-nutation signals.
Experimental results on the transient optical nutation effect inside an acetylene-filled hollow-core photonic crystal fiber (HC-PCF) are reported. The experiments used 15 ns optical pulses with peak powers up to 5 W. The light wavelength was centered at 1530.37 nm, which corresponds to the P9 acetylene (12C2H2) vibrational-rotational absorption line. The gas pressure inside the PCF, with hollow core diameter of ∼10.3 μm, was kept around 0.12 Torr. Comparison of the experimental data with numerical simulations using the Maxwell-Bloch equations allowed us to evaluate the characteristic longitudinal and transverse relaxation times around 10 ns, as well as the transition dipole moment (1.36 × 10−32 Cm).
We report detailed experimental results on the optical nutation effect in acetylene-filled hollow-core photonic crystal fibers (HC-PCFs). This coherent quantum optical effect is manifested by the appearance of attenuated oscillations in the profiles of transmitted step-like coherent optical pulses. The experiments used 15 ns optical pulses with peak powers up to ∼4 W and centered at 1530.37 nm, which corresponds to the acetylene (12C2H2) vibration-rotation resonance absorption line P9. The all-fiber cell made from a HC-PCF with internal diameter ∼10.3 μm contained a gas pressure of about 0.12 Torr. The Maxwell-Bloch equations are used to analyze the influence of the homogeneous relaxation, the inhomogeneous Doppler broadening of the absorption line, and the random orientation of the acetylene molecules. By comparing the experimental results with numerical simulations, we obtain the longitudinal and the transverse relaxation times to be close to 10 ns and find that the transition dipole moment of the acetylene P9 absorption line is ∼1.36×10−32 Cm.
Experimental observations of nonstationary coherent optical phenomena, i.e., optical nutation, free induction, and photon echo, in the acetylene (12{}^{12}12C2{}_{2}2​H2{}_{2}2​) filled hollow-core photonic-crystal fiber (PCF) are reported. The presented results were obtained for the acetylene vibration-rotational transition $P$9 at wavelength 1530.37 nm at room temperature under a gas pressure of 0.5 Torr. An all-fiber pumped-through cell based on the commercial 2.6-m-long PCF with a 10-\ensuremath{\mu}m hollow-core diameter was used. The characteristic relaxation time T2{T}_{2}T2​ during which the optical coherent effects were typically observed in our experiments was estimated to be \ensuremath{\approx}8 ns. This time is governed by the limited time of the acetylene molecules' presence inside the effective PCF modal area and by intermolecule collisions. An accelerated attenuation of the optical nutation oscillations is explained by a random orientation of acetylene molecules.
Analysis of influence of the Maxwell distribution of the transverse thermal velocities and of the flight-time-determined characteristic relaxation rates (i.e. the inverse relaxation times T1,2) of the acetylene (C2H2) molecules in the hollow-core photonic crystal fiber on nonlinear optical effects are presented. The theoretical predictions are compared with the experimental data obtained in the ~0.4Torr acetylene-filled fiber cell at the wavelength 1530.37nm of the most effective P9 vibrational-rotational transition of 12C2H2. At room temperature and the fiber mode field diameter of 7.5 μm, the average transverse thermal velocity of ~390m/s ensured relaxation times T1,2 ~8-10ns. These are in good agreement with the corresponding values experimentally measured using delayed optical nutation and two-photon echo techniques. The experimentally observed nonlinear effect of the polarization ellipse self-rotation proves to be at least two orders of magnitude less efficient comparing with that reported earlier for the alkali metals vapors.
In this work we report on the observation of photon echo inside acetylene-filled hollow-core photonic crystal fibers. The experiments were performed using a sequence of two short (~2ns) optical pulses tuned to the P9 (1530.37 nm) acetylene absorption line. The photon echo effect was observed on the basis of high optical powers (~4 W) and in the acetylene’s low pressure regime <0.5 Torr. The main results prove the formation of photon echo by showing that the obtained echo signals are consistent with the expected behavior, in intensity and optical delay, under variations of the input pulse separation.