The interaction of laser pulses with the Cauliflower mosaic virus (CaMV) in a Tris-HCl pH7.5 buffer is investigated. 20 ns ruby laser pulses are used for excitation. Spectra of the light passing through the sample and reflected from it are registered with the help of a Fabri-Perot interferometer. Stimulated low-frequency Raman scattering (SLFRS) in a CaMV suspension is registered. The SLFRS frequency shift, conversion efficiency and threshold are measured for the first time, to the best of our knowledge.
Laser pulses interaction with tobacco mosaic virus (TMV) in Tris-HCl pH7.5 buffer and in water has been investigated. 20 ns ruby laser pulses have been used for excitation. Spectrum of the light passing through the sample was registered with the help of Fabri-Perot interferometer. In the case of TMV in water we observed in the spectrum only one line of the exciting laser light, for TMV in Tris-HCl pH7.5 buffer second line appeared, corresponding to the stimulated low-frequency Raman scattering (SLFRS) on the breathing radial mode of TMV. SLFRS frequency shift by 2 cm-1, (60 GHz), conversion efficiency and threshold are measured for the first time to the best of our knowledge.
We present the development and performance of a Fourier transformation (FT) based Raman spectrometer working with visible laser (532 nm) excitation. It is generally thought that FT-Raman spectrometers are not viable in the visible range where shot-noise limits the detector performance and therein they are outperformed by grating based, dispersive ones. We show that contrary to this common belief, the recent advances of high-performance interference filters makes the FT-Raman design a valid alternative to dispersive Raman spectrometers for samples which do not luminesce. We critically compare the performance of our spectrometer to two dispersive ones: a home-built single channel and a state-of-the-art CCD based instruments. We demonstrate a similar or even better sensitivity than the CCD based dispersive spectrometer particularly when the laser power density is considered. The instrument possesses all the known advantages of the FT principle of spectral accuracy, high throughput, and economic design. We also discuss the general considerations which helps the community reassess the utility of the different Raman spectrometer designs.
Ultrashort long-wave infrared (LWIR) laser pulses can resonantly excite vibrations in N2 and O2 through a two-photon transition. The absorptive, vibrational component of the ultrafast optical nonlinearity grows in time, starting smaller than, but quickly surpassing, the electronic, rotational, and vibrational refractive components. The growth of the vibrational component results in a novel mechanism of 3rd harmonic generation, providing an additional two-photon excitation channel, fundamental + 3rd harmonic. The original and emergent two-photon excitations drive the resonance exactly out of phase, causing spatial decay of the absorptive, vibrational nonlinearity. This nearly eliminates two-photon vibrational absorption. Here we present simulations and analytical calculations demonstrating how these processes modify the ultrafast optical nonlinearity in air. The results reveal nonlinear optical phenomena unique to the LWIR regime of ultrashort pulse propagation in atmosphere.
We show that a 1.13-GHz repetition rate optical pulse train with 0.70 fs high-frequency timing jitter (integration bandwidth of 17.5 kHz - 10 MHz, where the measurement instrument-limited noise floor contributes 0.41 fs in 10 MHz bandwidth) can be directly generated from a free-running, single-mode diode-pumped Yb:KYW laser mode-locked by single-walled carbon nanotube (SWCNT)-coated mirrors. To our knowledge, this is the lowest timing jitter optical pulse train with the GHz repetition rate ever measured. If this pulse train is used for direct sampling of 565-MHz signals (Nyquist frequency of the pulse train), the demonstrated jitter level corresponds to the projected effective-number-of-bit (ENOB) of 17.8, which is much higher than the thermal noise limit of 50-ohm load resistance (~14 bits).
Detection and characterization of individual nano-scale particles, virions, and pathogens are of paramount importance to human health, homeland security, diagnostic and environmental monitoring[1]. There is a strong demand for high-resolution, portable, and cost-effective systems to make label-free detection and measurement of individual nanoparticles, molecules, and viruses [2-6]. Here, we report an easily accessible, real-time and label-free detection method with single nanoparticle resolution that surpasses detection limit of existing micro- and nano-photonic devices. This is achieved by using an ultra-narrow linewidth whispering gallery microlaser, whose lasing line undergoes frequency splitting upon the binding of individual nano-objects. We demonstrate detection of polystyrene and gold nanoparticles as small as 15 nm and 10 nm in radius, respectively, and Influenza A virions by monitoring changes in self-heterodyning beat note of the split lasing modes. Experiments are performed in both air and aqueous environment. The built-in self-heterodyne interferometric method achieved in a microlaser provides a self-reference scheme with extraordinary sensitivity [7,8], and paves the way for detection and spectroscopy of nano-scale objects using micro- and nano-lasers.
N. V. Tcherniega
,S. M. Pershin
,A. F. Bunkin
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(2018)
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"Laser excitation of gigahertz vibrations in Cauliflower mosaic viruses suspension"
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Nikolay Tcherniega V.
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