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Prospects for average power scaling of sub-MW output peak power picosecond fiber lasers by utilization of a Yb-doped tapered fiber at the final amplification stage were studied. In this paper, it was shown experimentally that a tapered fiber allows the achievement of an average power level of 150 W (limited by the available pump power) with a peak power of 0.74 MW for 22 ps pulses with no signs of transverse mode instability. Measurements of the mode content using the S2 technique showed a negligible level of high order modes (less than 0.3%) in the output radiation even for the maximum output power level. Our reliability tests predict no thermal issues during long-term operation (105 hours) of the developed tapered fiber laser up to kilowatt output average power levels.
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Luminescence emission and excitation spectra of bismuth-doped silica optical fibers free of other dopants have been obtained to construct an emission-excitation map in a wide wavelength range of 400-1600 nm. The main low-lying energy levels of the bismuth active centers in such fibers have been determined. For the first time (to our knowledge), optical gain and lasing have been obtained in such fibers. A gain of 8 dB has been achieved with a pump power of 340 mW, and a cw fiber laser emitting at 1460 nm with an output power of 40 mW and an efficiency of ≈3% has been created.
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The dynamics of glass-forming liquids under nanoconfinement is key to understanding a variety of phenomena in nature and modern technology. We report a (13)C NMR spectroscopic study that directly demonstrates that alpha-relaxation in bulk glycerol involves an isotropic rotational jump of the constituent molecules. The activation energy of this motion is approximately 78 kJ mol(-1) in the bulk, which abruptly changes to a low value of approximately 27.5 kJ mol(-1), characteristic of beta-processes, upon confinement of glycerol into approximately 2 nm pores in mesoporous silica. This observation implies that the molecular dynamics associated with structural relaxation near glass transition are inherently different in supercooled glycerol in the bulk and under extreme nanoconfinement.
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A photonic crystal fiber with a germanosilicate core having a nonlinear coefficient of 40 (W km)(-1) near the single dispersion zero at 1.09 microm is fabricated and studied. Broadband parametric wavelength conversion of the Ti:sapphire laser output tunable at 0.8 microm to the 1.55 microm band is obtained at 1.064 microm cw pump. The tuning of the converted signal in the 300 nm range was first realized without variation of the pump wavelength.
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The vibrational density of states (VDOS) for water confined on the surface of rutile-TiO(2) nanoparticles has been extracted from low temperature inelastic neutron scattering spectra. Two rutile-TiO(2) nanoparticle samples that differ in their respective levels of hydration, namely TiO(2) x 0.37 H(2)O (1) and TiO(2) x 0.22 H(2)O (2) have been studied. The temperature dependency of the heat capacities for the two samples has been quantified from the VDOS. The results from this study are compared with previously reported data for water confined on anatase-TiO(2) nanoparticles.
Assuntos
Nanopartículas/química , Nêutrons , Espalhamento de Radiação , Titânio/química , Água/química , Temperatura , Termodinâmica , VibraçãoRESUMO
Via imaging ellipsometry, we study the phase transition dynamics induced by selective gelation of one component in a binary supported phopholipid bilayer. We find the modulation of two attendant morphological features: emergence of extended defect chains due to a net change in the molecular areas and fractal-like domains suggesting weak line tension. A time-lapse analysis of the ellipsometric images reveals the cluster size of 4-20 molecules undergoing gelation indicating weak cooperativity. These results demonstrate the use of ellipsometry for in situ, label-free, non-contact, and large-area imaging of dynamics in interfacial films.
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Inelastic neutron scattering has been employed to probe the vibrational density of states of water confined by an oxide surface, namely, nanoparticles of the anatase polymorph of TiO2. The heat capacity of confined water has been measured by adiabatic calorimetry and compared with values derived from the vibrational density of states. Both inelastic neutron scattering and calorimetry demonstrate restricted mobility and lower heat capacity and entropy of confined water as compared to the bulk.
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Mesoporous silica phases, with uniform pores of dimensions in the 2-30 nm range, offer a uniquely well-defined environment for the study of the effects of two-dimensional spatial confinement on the properties of glass-forming liquids. We report observations by differential scanning calorimetry of the vitrification of o-terphenyl (OTP), salol, and glycerol in hexagonal mesoporous silica (MCM-41 and SBA-15) in a wide range of pore sizes from 2.6 to 26.4 nm. In agreement with previous studies, where a controlled porous glass is used as a solid matrix, the glass transition temperature for o-terphenyl diminishes with decreasing pore size. In contrast to OTP, glycerol shows a gradual increase in glass transition temperature, while in salol a slight reduction of glass transition temperature is observed, followed by an increase, which results in glass transition temperature indistinguishable from that of the bulk for the smallest pores. These results are discussed in terms of liquid-surface interactions in an interfacial layer, monitored by Fourier-transformed infrared spectroscopy in the study. The hydrogen bonding with silica surface silanols dominates the glass transition trends observed in salol and glycerol.