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arXiv:2603.21734 · Optica

Highly efficient perturbative Raman shifting by engineering the nonlinear temporal response

Yi-Hao Chen, Wenchao Wang, 侯绍东, José Enrique Antonio-Lopez, Rodrigo Amezcua‐Correa, Chris Xu, Frank W. Wise

Published Oct 8, 2026• 0 citations
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Abstract

Raman scattering underlies a broad range of spectroscopic and light-generation techniques, yet its conventional description, based on the Raman gain spectrum, accurately describes only long-pulse, steady-state dynamics. We employ a time-domain theoretical approach to account for spectrotemporal aspects of continuous frequency-shifting, which are not addressed by prior theories. In particular, molecules with strong Raman responses do not produce an efficient soliton self-frequency shift in gas-filled hollow-core fibers. The time-domain analysis exposes temporal and spectral distortions from the Raman response that impact frequency-shifting detrimentally, and identifies how these distortions can be suppressed by reducing the Raman interaction to a perturbation on the electronic response. Experiments that employ gas mixtures with tunable Raman fractions of the nonlinear response demonstrate up to a four-fold increase in quantum efficiency (from 20% to 80%) compared to the pure molecular gas, and unity-efficiency Raman shifting will be possible. The time-domain framework uncovers phenomena that are inaccessible through the frequency-domain treatment of Raman scattering, and it applies to Raman interactions in solids, liquids, and gases across Raman temporal regimes.

DOI
10.1364/optica.601914

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Raman scattering underlies a broad range of spectroscopic and light-generation techniques, yet its conventional description, based on the Raman gain spectrum, accurately describes only long-pulse, steady-state dynamics. We employ a time-domain theoretical approach to account for spectrotemporal aspects of continuous frequency-shifting, which are not addressed by prior theories. In particular, molecules with strong Raman responses do not produce an efficient soliton self-frequency shift in gas-filled hollow-core fibers. The time-domain analysis exposes temporal and spectral distortions from the Raman response that impact frequency-shifting detrimentally, and identifies how these distortions can be suppressed by reducing the Raman interaction to a perturbation on the electronic response. Experiments that employ gas mixtures with tunable Raman fractions of the nonlinear response demonstrate up to a four-fold increase in quantum efficiency (from 20% to 80%) compared to the pure molecular gas, and unity-efficiency Raman shifting will be possible. The time-domain framework uncovers phenomena that are inaccessible through the frequency-domain treatment of Raman scattering, and it applies to Raman interactions in solids, liquids, and gases across Raman temporal regimes.
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Backward stimulated Raman scattering in gases provides a promising route to the compression and amplification of a Stokes seed pulse by counter-propagating against a pump pulse, as has been demonstrated already in various platforms, mainly in free space. However, the dynamics governing this process when seeded by noise has not yet been investigated in a fully controllable collinear environment. Here we report, to the best of our knowledge, the first unambiguous observation of efficient noise-seeded backward stimulated Raman scattering in a hydrogen-filled hollow-core photonic crystal fiber. At high gas pressures, when the backward Raman gain is comparable to, but lower than, the forward gain, we report quantum conversion efficiencies exceeding 40% to the backward Stokes at 683 nm from a narrowband 532 nm pump. Efficiency increases to 65% when the backward process is seeded by a small amount of back-reflected forward-generated Stokes light. At high pump powers, the backward Stokes signal, emitted in a clean fundamental mode and spectrally pure, is unexpectedly always stronger than its forward-propagating counterpart. We attribute this striking observation to the unique temporal dynamics of the interacting fields, which cause the Raman coherence (which takes the form of a moving fine-period Bragg grating) to grow in strength toward the input end of the fiber. A good understanding of this process, together with the rapid development of novel anti-resonant-guiding hollow-core fibers, may lead to improved designs of efficient gas-based Raman lasers and amplifiers operating at wavelengths from the ultraviolet to the mid-infrared.
Unlike spontaneous Raman effect, nonlinear Raman scattering generates fields with a well-defined phase, allowing Raman signals from individual scatterers to add up into a highly directional, high-brightness coherent beam. Here, we show that the phase of coherent Raman scattering can be accurately controlled and finely tuned by using spectrally and temporally tailored optical driver fields. In our experiments, performed with spectrally optimized phase-tunable laser pulses, such a phase control is visualized through the interference of the coherent Raman signal with the field resulting from nonresonant four-wave mixing. This interference gives rise to Fano-type profiles in the overall nonlinear response measured as a function of the delay time between the laser pulses, featuring a well-resolved destructive-interference dip on the dark side of the Raman peak. This phase-control strategy is shown to radically enhance the coherent response from weak Raman modes, thus helping confront long-standing challenges in nonlinear Raman imaging and microspectroscopy.