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Advanced Solid-State Photonics (TOPS)

Efficient Broadband Raman Generation in Diamond Driven by multi-frequency femtosecond pulses

Xi Wang, Miaochan Zhi, Alexei V. Sokolov

Published Jan 1, 2009• 0 citations
Publisher

Abstract

We demonstrate efficient generation of multiple spatially-separated and frequency-shifted anti-Stokes and Stokes sidebands due to strong near-resonant excitation of Raman transition by crossing two- or three-color femtosecond laser pulses into diamond.
DOI
10.1364/assp.2009.tub21

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Physical Review A•Jul 18, 2005•34 citations
We demonstrate broadband light generation in diamond pumped by two-color femtosecond laser pulses. We find that phase matching plays a critical role in the output angle and frequency of the generated sidebands. When a third femtosecond probe pulse is applied to the crystal in the boxed Coherent anti-Stokes Raman Scattering geometry, a two-dimensional array of multi-color beams is generated through the Raman, four-wave mixing, and six-wave-mixing processes. We test the mutual coherence between the generated sidebands. Such coherence, maintained over the broad spectrum, opens possibilities for synthesis of subfemtosecond light waveforms.
Subfemtosecond pulses can be generated in a Raman generator by using electromagnetically induced transparency if ultrabroad Raman sidebands are generated and then propagate in such a way that the generated sidebands at higher frequencies are temporally advanced with regard to those at lower frequencies. However, it was recently demonstrated by experiments [1] that above-resonance Raman excitations ensured the establishment of anti-phased Raman coherence for pulse compression but only very limited number of Raman sidebands could be generated due to Raman self-defocusing [2], while broadband sidebands could be generated under below-resonance Raman excitations, which supported no pulse compression in the same Raman media. In order to establish anti-phased Raman coherence and simultaneously overcome Raman self-defocusing to benefit efficient generation of broadband sidebands, we suggest in this report a new technique to generate sub-fs pulse train in a Raman generator driven by three sufficiently intense single-mode laser beams whose carrier frequencies are tuned off the Raman resonance with two different two-photon detunings. The Raman interaction establishes a molecular modulation through nonadibatic processes. The simulation on the basis of the fundamental rotational Raman transitions in H2 shows that sub-fs pulse can be generated by above-resonance or below-resonance Raman excitations, or even Raman excitations with opposite detunings, as is shown in Fig.1. This opens a new way for experiments to observe enhanced generation of broadband Raman sidebands, together with compression of the phase-locked Raman sidebands into sub-fs pulse trains in the same Raman media
A pair of time-delayed linearly chirped pulses with sub-picosecond duration is used to selectively excite Raman transitions in a lead tungstate crystal. Significant molecular coherence leads to generation of up to 40 anti-Stokes and 5 Stokes sidebands. High conversion efficiency (from the two pump beams to the sidebands) is measured. The broadband generation with chirped pulses whose duration is comparable to the Raman coherence lifetime is considerably more efficient, when compared to the case of excitation by two-color femtosecond pulses. In the future, mutual coherence among the generated sidebands may allow ultrashort pulse synthesis.
In this work, we study the correlated Stokes-anti-Stokes (SaS) Raman scattering in a diamond sample and the influence that the excitation pulse width has in the intensity of generation of the correlated pairs in the process. For this investigation, we used two excitation systems with different temporal pulse width, one with femtosecond temporal width and one with picosecond temporal width. We did two distinct experiments with this excitation systems with difference in the way of filtering the signal: In the first experiment, the signal filtering is made with band-pass filters, this configuration has a greater efficiency that allow us compare better the correlated pair formation efficiency between the different excitation systems. In the second experiment, we used a monochromator to filtering the signal, this configuration allow us to change the wavelength of the detection so we can measure the formation spectrum of the correlated pairs. The results obtained from these experiments show us that the correlated pairs generation efficiency is larger with the use of the system with femtosecond temporal width, what is expected for a non-linear process. In the resonant Raman frequency region, we observed a intensity 1.5 times larger with the use of femtosecond system, and in the out-of-ressonance Raman region, we observed a intensity 5 times larger in the region with lowest Raman shift and 9 times larger in the region with largest Raman shift. We also measure the formation pairs spectrum around the first order Raman peak of the diamond, confirming the existence of a asymmetry in the formation of this pairs with respect to the positive versus negative detuning from phonon resonance. This asymmetry still remains without a satisfactory theoretical explanation.
We report pulse-shaper-assisted phase control of a broad spectrum, aiming to synthesize nonsinusoidal waveforms. We first generate multiple-order coherent Raman sidebands by focusing two laser beams into a piece of diamond. Then we combine five sidebands into a single beam by using a prism. Our setup allows for both coarse, manual phase adjustments and fine tuning of the spectral phases. A flat spectral phase across these five frequency-separated sub-bands is achieved, which implies generation of two to three optical-cycle pulses.
We have investigated the behavior of high-order stimulated Raman scattering in a highly-transient regime. We demonstrate efficient collinear generation of vibrational sidebands in molecular hydrogen and methane using two-color pumping with pulses of duration $\ensuremath{\tau}\ensuremath{\sim}100\phantom{\rule{0.3em}{0ex}}\mathrm{fs}$ tuned to a vibrational Raman transition. A Raman spectrum with a large bandwidth was observed, ranging from the IR to the UV. Under some conditions strong pump depletion was observed and up to five anti-Stokes sidebands were observed to have energies exceeding 10% of the transmitted pump pulse energies. A numerical simulation reproduces qualitatively and quantitatively the experimental results and allows us to explain key experimental features. The simulation also confirms that the molecular coherence in the medium is substantially increased by the two-color pumping and allows us to deduce values for the degree of material excitation. The use of this technique looks promising for efficient subfemtosecond pulse generation.