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Laser-induced white emission of diamond was investigated under irradiation with a focused beam of an infrared laser diode. It is a surface-related coherent emission, characterized by an excitation threshold and an exponential dependence on pumping laser power. The mechanism of white emission is discussed in terms of multiphoton ionization of carbon atoms in an irradiated spot. The excitation power dependence of white emission intensity has demonstrated hysteresis loop behavior. This phenomenon could be useful in new broadband laser sources and optical information storage.

This paper focuses on the kinetics of Cr 4+ formation in Cr,Ca:YAG ceramics prepared by solid-state reaction sintering. The kinetics of Cr 4+ formation was studied by annealing of Cr,Ca:YAG ceramics in ambient air under different temperatures at different times, resulting in the transformation of Cr 3+ to Cr 4+ . The activation energy (E a ) of Cr 3+ oxidation determined by the Jander model was 2.7 ± 0.2 eV, which is in good correlation with the activation energy of innergrain oxygen diffusion in the YAG lattice. It is concluded that Cr 3+ to Cr 4+ transformation in YAG ceramics is limited by oxygen diffusion through the grain body. It was established that in Cr,Ca:YAG ceramics, the intralattice cation exchange, in which the Cr 4+ ions exchange positions with the Al 3+ ions, switching from "A" to "D" sites, is faster than Cr 3+ to Cr 4+ oxidation. In the temperature range of 900-1300 °C, the reaction enthalpy of Al 3+ /Cr 4+ ion exchange between octahedral "A" and tetrahedral "D" lattice sites is close to zero, and this exchange ratio is thermodynamically driven by entropy.

The up-converting nanocrystals of KLa0.95Er0.05Y bxP4O12 and La0.95-xEr0.05Y bxP5O14 were prepared using co-precipitation method. The spectroscopic properties of these materials were investigated in a function of Y b(3+) concentration. The up-conversion emission, power dependence of emission intensities, and the luminescence decay times were investigated. It was found that the green to red and (2)H11/2 → (4)I15/2 to (4)S3/2 → (4)I15/2 emission intensity ratio were strongly affected by the Y b(3+) concentration. Moreover, the order of up-conversion emission and threshold power rises up with Y b(3+) concentration for (4)S3/2 → (4)I15/2 transition. The luminescence decay time of the (4)S3/2 → (4)I15/2 emission increases with Y b(3+) concentration while the (4)F9/2 → (4)I15/2 emission is independent of dopant concentration. The influence of the Y b(3+) concentration on the up-conversion emission intensities was discussed in terms of concentration dependent hetero looped photon avalanche process. A comparison of the up-conversion properties of KLa0.95Er0.05Y bxP4O12 and La0.95-xEr0.05Y bxP5O14 nanocrystals was presented.