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Yuexin Wan

Publications and source records attributed to Yuexin Wan.

3 recordsLinked to original sources

Photon retention in coherently excited nitrogen ions

Quantum coherence in quantum optics is an essential part of optical information processing and light manipulation. Alkali metal vapors, despite the numerous shortcomings, are traditionally used in quantum optics as a working medium due to convenient near-infrared excitation, strong dipole transitions and long-lived coherence. Here, we proposed and experimentally demonstrated photon retention and subsequent re-emittance with the quantum coherence in a system of coherently excited molecular nitrogen ions (N2+) which are produced using a strong 800 nm femtosecond laser pulse. Such photon retention, facilitated by quantum coherence, keeps releasing directly-unmeasurable coherent photons for tens of picoseconds, but is able to be read-out by a time-delayed femtosecond pulse centered at 1580 nm via two-photon resonant absorption, resulting in a strong radiation at 329.3 nm. We reveal a pivotal role of the excited-state population to transmit such extremely weak re-emitted photons in this system. This new finding unveils the nature of the coherent quantum control in N2+ for the potential platform for optical information storage in the remote atmosphere, and facilitates further exploration of fundamental interactions in the quantum optical platform with strong-field ionized molecules.

quant-ph

A spectrally bright wavelength-switchable vacuum ultraviolet source driven by quantum coherence in strong-field-ionized molecules

We report generation of spectrally bright vacuum ultraviolet (VUV) and deep UV (DUV) coherent radiations driven by quantum coherence in tunnel-ionized carbon monoxide (CO) molecules. Our technique allows us to switch between multiple wavelengths provided by the abundant energy levels of molecular ions. The DUV/VUV sources can have arbitrary polarization states by manipulating the pump laser polarization. The superior temporal and spectral properties of the developed source give rise to a broadband Raman comb in the DUV/VUV region.

physics.optics

Extreme nonlinear Raman interaction of an ultrashort nitrogen ion laser with an impulsively excited molecular wavepacket

We report generation of cascaded rotational Raman scattering up to 58th orders in coherently excited CO_2 molecules. The high-order Raman scattering, which produces a quasiperiodic frequency comb with more than 600 sidebands, is obtained using an intense femtosecond laser to impulsively excite rotational coherence and the femtosecond-laser-induced N_2^+ lasing to generate cascaded Raman signals. The novel configuration allows this experiment to be performed with a single femtosecond laser beam at free-space standoff locations. It is revealed that the efficient spectral extension of Raman signals is attributed to the specific spectra-temporal structures of N_2^+ lasing, the ideal spatial overlap of femtosecond laser and N2+ lasing, and the guiding effect of molecular alignment. The Raman spectrum extending above 2000 cm^-1 naturally corresponds to a femtosecond pulse train due to the periodic revivals of molecular rotational wavepackets.

physics.optics