ترغب بنشر مسار تعليمي؟ اضغط هنا

Optical absorption and structure of impurity Ni$^{2+}$ center in tungstate-tellurite glass

64   0   0.0 ( 0 )
 نشر من قبل Vyacheslav Sokolov
 تاريخ النشر 2011
  مجال البحث فيزياء
والبحث باللغة English




اسأل ChatGPT حول البحث

Absorption spectra of Ni$^{2+}$ ions in 22WO$_3$--78TeO$_2$ tungstate-tellurite glass were studied and Ni$^{2+}$ extinction coefficient spectral dependence was derived in the 450 -- 2700 nm wavelength range. Computer modeling of the glass structure proved Ni$^{2+}$ ions to be in trigonal-distorted octahedral environment in the tungstate-tellurite glass. Tanabe-Sugano diagram for such an environment was calculated and good description of the observed spectrum of Ni$^{2+}$ ion was obtained. Basing on both absorption spectral range width and the extinction coefficient, nickel should be considered among the most strongly absorbing impurities in the tellurite glasses.

قيم البحث

اقرأ أيضاً

Quantifying temperature variations at the micron scale can provide new opportunities in optical sensing. In this paper, we present a novel approach using the temperature-dependent variations in fluorescence of rare-earth doped tellurite glass to prov ide a micron-scale image of temperature variations over a 200 micrometre field of view. We demonstrate the system by monitoring the evaporation of a water droplet and report a net temperature change of 7.04 K with a sensitivity of at least 0.12 K. These results establish the practicality of this confocal-based approach to provide high-resolution marker-free optical temperature sensing.
We report the infrared transmission measurement on electrically gated twisted bilayer graphene. The optical absorption spectrum clearly manifests the dramatic changes such as the splitting of inter-linear-band absorption step, the shift of inter-van Hove singularity transition peak, and the emergence of very strong intra-valence (intra-conduction) band transition. These anomalous optical behaviors demonstrate consistently the non-rigid band structure modification created by the ion-gel gating through the layer-dependent Coulomb screening. We propose that this screening-driven band modification is an universal phenomenon that persists to other bilayer crystals in general, establishing the electrical gating as a versatile technique to engineer the band structures and to create new types of optical absorptions that can be exploited in electro-optical device application.
Band gap engineering in SrTiO${}_{3}$ and related titanate perovskites has long been explored due to the intriguing properties of the materials for photocatalysis and photovoltaic applications. A popular approach in the materials chemistry community is to substitutionally dope aliovalent transition metal ions onto the B site in the lattice to alter the valence band. However, in such a scheme there is limited control over the dopant valence, and compensating defects often form. Here we demonstrate a novel technique to controllably synthesize Fe$^{2+}$- and Fe$^{3+}$-doped SrTiO${}_{3}$ thin films without formation of compensating defects by co-doping with La$^{3+}$ ions on the A site. We stabilize Fe$^{2+}$-doped films by doping with two La ions for every Fe dopant, and find that the Fe ions exhibit a low-spin electronic configuration, producing optical transitions in the near infrared regime and degenerate doping. The novel electronic states observed here offer a new avenue for band gap engineering in perovskites for photocatalytic and photovoltaic applications.
Tellurite glass fibers with embedded nanodiamond are attractive materials for quantum photonic applications. Reducing the loss of these fibers in the 600-800 nm wavelength range of nanodiamond fluorescence is essential to exploit the unique propertie s of nanodiamond in the new hybrid material. In the first part of this study, we report the effect of interaction of the tellurite glass melt with the embedded nanodiamond on the loss of the glasses. The glass fabrication conditions such as melting temperature and concentration of NDs added to the melt were found to have critical influence on the interaction. Based on this understanding, we identified promising fabrication conditions for decreasing the loss to levels required for practical applications.
Window glass is a ternary mixture, while pyrex (after window glass, the most common form of commercial glass) is a quaternary. Building on our previous success in deriving the composition of window glass (sodium calcium silicate) without adjustable p arameters, and borrowing from known reconstructed crystalline surfaces, we model pyrex as silica clusters with a specific ternary interface. Our global model explains the thermal expansivity contours of ternary sodium borosilicates, and it is consistent with the optimized resistance of pyrex to mechanical and thermal shocks. It suggests new directions for studying the nanoscopic structure of these remarkable materials.
التعليقات
جاري جلب التعليقات جاري جلب التعليقات
سجل دخول لتتمكن من متابعة معايير البحث التي قمت باختيارها
mircosoft-partner

هل ترغب بارسال اشعارات عن اخر التحديثات في شمرا-اكاديميا