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    Long-wavelength spectral shift in an ultraviolet filament

    D. E. Shipilo1,2,*, N. R. Vrublevskaya1,2, I. A. Nikolaeva1,2, L. V. Seleznev1,2, D. V. Pushkarev1,2, G. E. Rizaev1,2, M. V. Levus1,2, A. A. Ionin2, N. A. Panov1,2 et al.

    O. G. Kosareva1,2,†

    • *Contact author: schipilo.daniil@physics.msu.ru
    • †Contact author: kosareva@physics.msu.ru

    Phys. Rev. A 112, 023516 – Published 22 August, 2025

    DOI: https://doi.org/10.1103/mgvk-wscf

    Abstract

    Our experiments on focusing of ultraviolet ∼250−nm, ∼100−fs, 0.2-mJ pulses into a cuvette filled with diatomic air or monatomic argon show similar spectral transformations regardless of the gas if the pressure is the same. The spectra experience broadening and the long-wavelength shift, which increases monotonically with the pressure and reaches 2 nm at 1 atm. This long-wavelength shift cannot be explained by instantaneous Kerr nonlinear response and multiphoton ionization as two additive contributions to the nonlinear refractive index. The simulations based on the 1D time-dependent Schrödinger equation reveal that the cubic nonlinearity is delayed by ∼100 as with regard to the driving field. This intraperiod delay comparable with the ∼800−as field cycle shifts the polarization spectrum to longer wavelengths and can be obtained solely from the quantum-mechanical approach, which we uniquely applied to the description of ultraviolet femtosecond filamentation.

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