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Though Pr3+ doped LiYF4 (LiYF4:Pr3+) bulk crystals are a well-known laser gain material with several radiative transitions, their nanocrystal counterparts have not been investigated with regards to these. Through downsizing to the nanoscale, novel applications are expected, especially in composite photonic devices. For example, nanocrystals in stable colloidal form with narrow size distribution are highly desirable to reduce scattering in such composites. Herein, we synthesized monodispersed LiYF4:Pr3+ nanocrystals having a size of 10 nm resulting in colorless clear stable colloidal dispersions and conducted an extensive optical characterization for the first time. We observed unexpected yet intense emission with excited state lifetimes comparable to bulk crystals in the visible spectrum through excitation at 444 nm and 479 nm. In macroscopic bulk crystals, this emission is only exploitable through excitation of a different, subjacent energy level. A comprehensive comparison to the bulk crystals provides deeper insight into the excitation mechanism and performance of these nanocrystals. The presented results pave the way for developing application-oriented LiYF4:Pr3+ nanocrystals as emitters with tailored properties for quantum optics or biomedical applications.

In recent years, optical nanothermometers have seen huge improvements in terms of precision as well as versatility, and several research efforts have been directed at adapting novel active materials or further optimizing the temperature sensitivity. The signal-to-noise ratio of the emission lines is commonly seen as the only limitation regarding high precision measurements. The role of re-absorption caused by a population of lower energy levels, however, has so far been neglected as a potential bottleneck for both high resolution and material selection. In this work, we conduct a study of the time dependent evolution of population densities in different luminescence nanothermometer classes under the commonly used pulsed excitation scheme. It is shown that the population of lower energy levels varies when the pump source fluctuates in terms of power and pulse duration. This leads to a significant degradation in temperature resolution, with limiting values of 0.5 K for common systems. Our study on the error margin indicates that either short pulsed or continuous excitation should be preferred for high precision measurements. Additionally, we derive conversion factors, enabling the re-calibration of currently available intensity ratio measurements to the steady state regime, thus facilitating the transition from pulse regimes to continuous excitation.

In recent years, lanthanide-doped nanothermometers have been mainly used in thin films or dispersed in organic solvents. However, both approaches have disadvantages such as the short interaction lengths of the active material with the pump beam or complicated handling, which can directly affect the achievable temperature resolution. We investigated the usability of a polymer fiber doped with upconversion nanocrystals as a thermometer. The fiber was excited with a wavelength stabilized diode laser at a wavelength of 976 nm. Emission spectra were recorded in a temperature range from 10 to 35◦C and the thermal emission changes were measured. Additionally, the pump power was varied to study the effect of self-induced heating on the thermometer specifications. Our fiber sensor shows a maximal thermal sensitivity of 1.45%/K and the minimal thermal resolution is below 20 mK. These results demonstrate that polymer fibers doped with nanocrystals constitute an attractive alternative to conventional fluorescence thermometers, as they add a long pump interaction length while also being insensitive to strong electrical fields or inert to bio-chemical environments. © 2020 by the authors. Licensee MDPI, Basel, Switzerland.

Updated Supplementary Text file with modified Figure S1

Updated Supplementary Text file with modified Figure S1

We present a comprehensive study of laser pulse amplification with respect to operation regimes, gain dynamics, and highly stable operation points of Ho:YLF regenerative amplifiers (RAs). The findings are expected to be more generic than for this specific case. Operation regimes are distinguished with respect to pulse energy and the appearance of pulse instability, and are studied as a function of the repetition rate, seed energy, and pump intensity. The corresponding gain dynamics are presented, identifying highly stable operation points related to high gain build -up during pumping and high gain depletion during pulse amplification. These operation points are studied numerically and experimentally as a function of several parameters, thereby achieving, for our Ho:YLF RA, highly stable output pulses with measured fluctuations of only 0.19% (standard deviation).

We present a method for the generation of complex pulse sequences by using periodic spectral phase modulation. An analytical expression is derived for the temporal profile of such pulse sequences, which relates the temporal amplitudes and phases of the subpulses to the Fourier components of the periodic phase mask. We consider two families of periodic phase masks, namely, when a single period is an odd or even function, and discuss the differences between the resulting pulse sequences. The ability to generate pulse sequences with more degrees of freedom provides an alternative parametrization for investigating quantum coherent control landscapes. This is illustrated in the context of dark pulses in nonresonant two-photon absorption., Comment: 5 pages and 3 figures. Comments are appreciated

We report on a mid-infrared frequency comb source of unprecedented tunability covering the entire 3-10 {\mu}m molecular fingerprint region. The system is based on difference frequency generation in a GaSe crystal pumped by a 151 MHz Yb:fiber frequency comb. The process was seeded with Raman shifted solitons generated in a highly nonlinear suspended-core fiber with the same source. Average powers up to 1.5 mW were achieved at 4.7 {\mu}m wavelength., Comment: 3 pages, 3 figures