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Optics Express

Generation of vacuum-ultraviolet pulses with a Doppler-broadened gas utilizing high atomic coherence

Li Deng, Takashi Nakajima

Published Jul 18, 2012• 5 citations
Publisher

Abstract

We carry out the theoretical study for the generation of vacuum-ultraviolet pulses with a Doppler-broadened gas utilizing high atomic coherence. It is essentially a difference-frequency generation scheme induced by the two-photon near-resonant pump and probe pulses, where the key point is to generate high atomic coherence between the ground and two-photon near-resonant states through a variant of stimulated Raman adiabatic passage with a time-dependent detuning. The advantage of our scheme is that the degree of coherence is sensitive to neither the exact amount and even sign of the detuning, nor the exact timing between the pump, auxiliary, and probe pulses. Hence our scheme is practically insensitive to Doppler broadening. As a specific example, we consider the generation of picosecond Lyman-α pulses with a Kr gas, and quantitatively study the influence of Doppler broadening as well as the intensity and incident timing of the picosecond probe pulse with respect to the pump pulse. The numerical results indicate that our scheme has a certain advantage over the conventional scheme which utilizes two-photon resonant excitation.

DOI
10.1364/oe.20.017566

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We carry out the theoretical study for the generation of vacuum-ultraviolet pulses with a Doppler-broadened gas utilizing high atomic coherence. It is essentially a difference-frequency generation scheme induced by the two-photon near-resonant pump and probe pulses, where the key point is to generate high atomic coherence between the ground and two-photon near-resonant states through a variant of stimulated Raman adiabatic passage with a time-dependent detuning. The advantage of our scheme is that the degree of coherence is sensitive to neither the exact amount and even sign of the detuning, nor the exact timing between the pump, auxiliary, and probe pulses. Hence our scheme is practically insensitive to Doppler broadening. As a specific example, we consider the generation of picosecond Lyman-α pulses with a Kr gas, and quantitatively study the influence of Doppler broadening as well as the intensity and incident timing of the picosecond probe pulse with respect to the pump pulse. The numerical results indicate that our scheme has a certain advantage over the conventional scheme which utilizes two-photon resonant excitation.
We present experimental data on adiabatically driven frequency conversion with ultrashort (picosecond) laser pulses towards the vacuum-ultraviolet regime, enhanced by coherent population return and preparation of maximal atomic coherences. We generate the sum frequency of an intense pump pulse and a probe pulse via a two-photon resonance in xenon. When we slightly detune the pump laser from two-photon resonance, the atomic populations are adiabatically driven forth and back from the atomic ground state to an excited state. This coherent population return (CPR) prepares the medium in a transient state of maximal atomic coherence, which enhances frequency mixing with a probe laser. We thoroughly study the variation of CPR-enhanced frequency conversion with experimental parameters and compare CPR with conventional, resonantly enhanced frequency conversion. In particular, we investigate the temporal evolution of the atomic coherence and the effect of inevitable ac Stark shifts. We find that ac Stark shifts induce an asymmetry in the spectral characteristics of CPR, which nevertheless permits enhanced frequency conversion. For the case of resonantly enhanced frequency conversion, we show that the atomic coherences are maintained for several tens of picoseconds after the pump pulse, which permits time-delayed frequency conversion. Moreover, we analyze the pressure dependence of the atomic coherence' lifetime and observe a free induction decay at the two-photon coherence with the generation of a second harmonic field. These findings shall push applications of adiabatic light-matter interactions also to the regime of nonlinear optics, driven by intense laser pulses.
Two-photon resonant and near-resonant four-wave difference-frequency mixing in gases in the interaction regime when laser pulse durations are comparable to or shorter than the medium polarization relaxation time ${T}_{2}^{\ensuremath{'}}$ is investigated. The results of experimental studies of the process in Ar and Kr using pump pulses from the ArF-excimer laser are presented demonstrating a generation of tunable short pulse radiation in the range 102--124 nm. The results are discussed in terms of a theoretical model based on a self-consistent solution of the Bloch equations for the atomic transitions and the Maxwell equations for the fields. This enables one to interpret specific nonstationary resonant and quasiresonant phenomena involved in the frequency conversion process. It is shown that the femtosecond-pulse four-wave frequency-mixing technique with probe pulses significantly shorter than the pump pulses makes it possible to study the coherent dynamics of an atomic transition exposed to an intense field. Using atomic Kr as the nonlinear medium, coherent Rabi oscillations and the subsequent phase relaxation of excitation were observed under the condition of two-photon interaction of Kr with femtosecond 193-nm laser pulses. The obtained information is important for controlling and optimizing processes of two-photon resonant frequency conversion and for time-resolved studies of Rydberg states in atoms and molecules.
We present an experimental demonstration of sum-frequency generation toward tunable picosecond, broadband radiation pulses in the extreme-ultraviolet regime, supported by adiabatically prepared atomic coherences. We drive a two-photon transition in a dense medium of xenon atoms with a long (nanosecond) pump laser pulse at the Fourier-transform-limited bandwidth and with a wavelength of 225 nm. The frequency of the pump pulse is slightly detuned from exact two-photon resonance. In this configuration, the medium is adiabatically driven by a process of coherent population return. The adiabatic passage process generates a maximal coherent superposition of two quantum states with large energy spacing. An additional, short (picosecond) probe laser pulse at a wavelength of 540 nm beats with the maximal atomic coherence and generates a short (picosecond) signal radiation pulse at 93 nm. As compared to conventional (diabatic) frequency conversion, the adiabatically driven maximal atomic coherence yields enhanced conversion efficiency and significantly enhanced stability.
A scheme is analyzed for effcient generation of vacuum ultraviolet radiation through four-wave mixing processes assisted by the technique of Stark-chirped rapid adiabatic passage. These opportunities are associated with pulse excitation of laddertype short-wavelength two-photon atomic or molecular transitions so that relaxation processes can be neglected. In this three-laser technique, a delayed-pulse of strong oR-resonant infrared radiation sweeps the laser-induced Stark-shift of a two-photon transition in a such way that facilitates robust maximum two-photon coherence induced by the first ultraviolet laser. A judiciously delayed third pulse scatters at this coherence and generates short-wavelength radiation. A theoretical analysis of these problems based on the density matrix is performed. A numerical model is developed to carry out simulations of a typical experiment. The results illustrate a behavior of populations, coherence and generated radiation along the medium as well as opportunities of effcient generation of deep (vacuum) ultraviolet radiation.
We theoretically study the generation of coherence in generalized two-level atoms with hyperfine structure by utilizing the detuning-induced stimulated Raman adiabatic passage (D-STIRAP). As expected, the degree of attainable coherence between the ground and excited states cannot be as large as that for the ideal two-level atoms without hyperfine structure. However, we find that the substantial degree of coherence can still be produced with small modulations, and the modulation period is essentially determined by the hyperfine splittings in the ground and excited states. The D-STIRAP scheme in generalized two-level atoms is sufficiently robust against the various parameters such as intensities of lasers, initial detuning, time delay between the laser pulses, and Doppler broadening. As a specific example, we show realistic results for the D1{D}_{1}D1​ transition of Na.
Recent techniques in x-ray free electron lasers allow the generation of highly coherent, intense x-ray pulses with time lengths on the order of femtoseconds. Here we explore the possibilities of using such x-ray pulses to control matter based on coherence. In particular we propose a theoretical scheme to perform stimulated Raman adiabatic passage in the x-ray regime by using inner-hole excited states. Numerical results in two well-known systems, the neon atom and the carbon monoxide molecule, show a robust control of population transfer. In the molecule, vibrational selectivity is achieved with femtosecond x-ray pulses. This work supports the possibility of using two-color x-ray pulses for coherent control.