We demonstrate experimentally and theoretically a controllable way of shifting the frequency of an optical pulse by using a combination of spectral hole burning, slow light effect, and linear Stark effect in a rare-earth-ion doped crystal. We claim that the solid angle of acceptance of a frequency shift structure can be close to 2π, which means that the frequency shifter could work not only for optical pulses propagating in a specific spatial mode but also for randomly scattered light. As the frequency shift is controlled solely by an external electric field, it works also for weak coherent light fields, and can e.g. be used as a frequency shifter for quantum memory devices in quantum communication.arXiv:1601.08058v1 [quant-ph]

Plasma-related studies in gas phase are challenging to carry out due to plasma’s transient and unpredictable behavior, excessive luminosity emission, 3D complexity and aggressive chemistry and physiochemical interactions that are easily affected by external probing. Laser-induced fluorescence is a robust technique for non-intrusive investigations of plasma-produced species. In this letter, we present 3D distributions of ground state hydroxyl radicals (OH) radicals in the vicinity of a glow-type gliding arc plasma. Such radical distributions are captured instantaneously in one single camera acquisition by combining structured laser illumination and a lock-in based imaging analysis method called FRAME. The interference of plasma emission is automatically subtracted by the FRAME technique. In addition, the orientation of the plasma discharge can be reconstructed from the 3D data matrix, which can then be used to calculate 2D distributions of ground state OH radicals in a plane perpendicular to the orientation of the plasma channel. Our results indicate that OH distributions around a gliding arc are strongly affected by gas dynamics. We believe that the ability to instantaneously capture 3D transient molecular distributions in a plasma discharge, with minimal plasma emission interference, will have a strong impact on the plasma community for in situ investigations of plasma-induced chemistry and physics.

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Streak cameras are central to measurements across the sciences. By spatially modulating the entrance slit, we show a more than 20% increase in temporal resolution opening up for sub-picosecond measurements with standard streak camera systems.

Plasma discharges can be transient and randomly distributed where a few investigations have been carried out using laser-induced fluorescence to capture snapshots of plasma-produced radicals in the near vicinity of the discharge. Radical distribution dynamics, however, are challenging to study in-situ with high spatial and temporal resolution to fully capture the interactions between the discharge and the gas. We here demonstrate a planar laser-induced fluorescence method that can capture molecular distributions of ground state hydroxyl radicals in a discharge plasma and follow how the distribution develops in time with a repetition rate of 27 kHz. The technique is demonstrated by monitoring, in real-time, how the tube-like distribution of ground state OH radicals, surrounding a gliding arc plasma, is affected by flow dynamics and how it develops as the high voltage is turned off at atmospheric pressure. The method presented here is an essential tool for capturing radical-distribution dynamics in-situ of chemically active environments which is the active region of the plasma induced chemistry.