Polarization switching in a long-wavelength vertical-cavity surface-emitting laser (VCSEL) under parallel optical injection is analyzed in a theoretical and experimental way. For the first time, to our knowledge, we report experimentally a state in which injection locking of the parallel polarization and excitation of the free-running orthogonal polarization of the VCSEL are simultaneously obtained. We obtain very simple analytical expressions that describe both linear polarizations. We show that the power of both linear polarizations depend linearly on the injected power in such a way that the total power emitted by the VCSEL is constant. We perform a linear stability analysis of this solution to characterize the region of parameters in which it can be observed. Our measurements qualitatively confirm the previous theoretical predictions.

We investigate experimentally and theoretically the polarization switching found in a single-transverse mode VCSEL when subject to parallel optical injection. Our analysis focuses on a recently observed state in which injection locking of the parallel polarization and excitation of the free-running orthogonal polarization of the VCSEL are obtained. A simple nonlinear dependence between the power of both linear polarizations and the frequency detuning is found. Also the total power emitted by the VCSEL is constant and independent on the injected optical power and on the frequency detuning. We check these results experimentally for a variety of frequency detunings and bias currents applied to the device. We report experimental and theoretical stability maps in the injected power-frequency detuning plane for different bias currents identifying the regions in which the state is observed. A simple analytical expression that describes the map boundary for large and negative frequency detunings is obtained. This provides a simple method to extract the linear dichroism of the device.

Examining the physical properties of materials - particularly of toxic liquids - under a wide range of thermodynamic states is a challenging problem due to the extreme conditions the material has to be exposed to. Such temperature and pressure regimes, which result in a change of refractive index and sound velocity can be accessed by optoacoustic interactions such as Brillouin-Mandelstam scattering. Here we experimentally demonstrate Brillouin-Mandelstam measurements of nanoliter volumes of liquids in extreme thermodynamic regimes. We use a fully-sealed liquid-core optical fiber containing carbon disulfide; within this waveguide, which exhibits tight optoacoustic confinement and a high Brillouin gain of 32.2 ± 0.8 1/(Wm), we are able to conduct spatially resolved measurements of the Brillouin frequency shift. Knowledge of the local Brillouin response enables us to control the temperature and pressure independently over a wide range. We observe and measure the material properties of the liquid core at very large positive pressures (above 1000 bar), substantial negative pressures (below -300 bar) and we explore the isobaric and isochoric regimes. The extensive thermodynamic control allows the tunability of the Brillouin frequency shift of more than 40% using only minute volumes of liquid. This work opens the way for future studies of liquids under a variety of conventionally hard-to-reach conditions.