Abstract

Results from the successful growth of high quality KH2PO4 (KDP) crystals with incorporated TiO2 anatase nanoparticles and the characterization of these crystals using several complementary methods are presented. The study allowed the nature and distribution of macroscopic and microscopic defects in the KDP:TiO2 crystals to be clarified. The relationship between these defects and the distribution of TiO2 nanoparticles, and the influence of incorporated nanoparticles on the nonlinear optical properties of composite crystals in comparison with pure crystals were also elucidated. Visual observations, transmission and scanning electron microscopy have shown that the anatase nanoparticles were captured mainly by the pyramidal growth sector and, to a considerably lesser extent, by the prismatic growth sector. Energy dispersive x-ray analysis was able to confirm that the growth layer stacks contain the TiO2 particles. Fourier transformation infrared spectra have clearly shown the presence of an absorption band at about 800 cm−1 in both KDP:TiO2 and TiO2, and the disappearance of the band, associated with hydroxyl OH− groups on the TiO2 surface in KDP:TiO2. Significant variation in the imaginary and real parts of the cubic nonlinear optical susceptibilities and refractive index changes at continuous wave excitation were found in prism and pyramid parts of pure KDP and KDP:TiO2 samples. Deciphering complicated electron paramagnetic resonance spectra in KDP:TiO2 and comparison with published data permitted the identification of paramagnetic defects along with their associated g-factors and zero-field splitting parameters (in some cases for the first time). It was found that the dominant lines belong to four different centers FeA3+, FeB3+, CrR3+, and CrGB3+. From analysis of line intensities it was concluded that the concentration of intrinsic defects like potassium and hydrogen vacancies in KDP:TiO2 is comparatively small, that the concentration of non-controlled impurities in nominally pure KDP samples is several times larger than in KDP:TiO2, and that the concentration of non-controlled impurities in the prismatic part of the KDP:TiO2 boule is approximately twice as large as in the pyramid part.

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