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Multimode near-stoichiometric (NS) Ti:LiNbO3 planar waveguide was fabricated by Ti-diffusion followed by post-Li-rich vapor transport equilibration. The crystalline phase, composition and guided modes in the planar waveguide were characterized. The refractive index profile in the waveguide is constructed from the measured mode indices using the inverse Wentzel–Krames–Brillouin method and correlated with the Ti profile obtained from secondary ion mass spectroscopy analysis. The results show that the LiNbO3 phase dominates in the waveguide layer and the waveguide has an NS composition. The index increase has a linear relation to Ti-concentration for both cases of ordinary and extraordinary rays, and the relationship is considerably different from those of some congruent or NS bulk materials or waveguides. A comparison of various congruent and NS bulk materials or waveguides allows to conclude that the relationship changes from congruent to NS composition, from one fabrication method to another and from bulk material to waveguide configuration. [ABSTRACT FROM PUBLISHER]

Zr4+/Ti4+-codoped LiNbO3 plates were prepared by local codiffusion of stacked ZrO2 and Ti metal films coated onto Z-cut congruent LiNbO3 substrates in wet O2 at 1060°C. The metal and oxide films have different thicknesses and coating sequences. After diffusion, the Zr4+ doping effect on the refractive index of LiNbO3 and the Li2O out-diffusion issue were studied by the prism coupling technique. The codiffusion characteristics of Zr4+ and Ti4+ were studied by secondary ion mass spectrometry. The results show that the Zr4+ doping has little contribution to the refractive index of the crystal. Li2O out-diffusion is not measurable. In the Zr4+-only diffusion case, the diffusivity of Zr4+ is four times smaller than that of Ti4+. In the Zr4+/Ti4+ codiffusion case, the Ti4+ codiffusion assists the Zr4+ diffusion. The Zr4+ diffusivity increases linearly by two more times with the increase in initial Ti film thickness from 0 to 200 nm. On the other hand, the Zr4+ affects the Ti4+ diffusion little. Neither the ZrO2 film thickness nor the coating sequence of Ti metal and ZrO2 oxide films influences the diffusivity of the two ions. All the codiffusion characteristics are explained. A Zr4+/Ti4+ codiffusion model is suggested that consists of two independent diffusion equations with a Zr4+ diffusivity dependent of Ti4+ concentration and a constant Ti4+ diffusivity. In addition, the existence of a waveguide in the Zr4+/Ti4+-codoped layer is verified experimentally, and the optical-damage-resistant feature of the waveguide is verified by two-beam hologram recording experimental results. [ABSTRACT FROM AUTHOR]

Multi-mode Ti:LiNbO 3 planar waveguide was fabricated by in-diffusion of 100-nm-thick Ti-metal film coated onto a near-stoichiometric LiNbO 3 substrate prepared by vapor transport equilibration. The crystalline phase and composition in the waveguide were characterized. The guided modes in the planar waveguide were characterized by prism coupling technique. The refractive index profile is constructed from the measured mode indices using the inverse Wentzel–Krames–Brillouin method, and correlated with the Ti 4+ - concentration profile, which was obtained from secondary-ion-mass-spectroscopy analysis. The results show that the waveguide still retains the LiNbO 3 phase, its composition is near-stoichiometric. The index change and Ti 4+ -concentration follow an exponential relationship with a power index 0.4 for an ordinary ray and 1.07 for an extraordinary ray. A comparison of various congruent and near-stoichiometric bulk materials or waveguides allows to conclude that the relationship is different from congruent to near-stoichiometric composition, from one fabrication method to another, and from bulk material to waveguide configuration. The difference is explained qualitatively. [ABSTRACT FROM AUTHOR]

The influence of factors on the growthof the Er3+/Tm3+-codoped LiNbO3(LN)crystal by codiffusion ofstacked Er and Tm metal thin films was studied. These factors includethe thicknesses and the coating sequence of the Er and Tm metal films,and the growth is characterized by the diffusivity and solubility.To achieve the goal, Er3+/Tm3+-codoped LN crystalswere grown by codiffusion in air at 1130 °C of stacked Er andTm metal thin films coated onto the surface of Z-cut congruent LNplates. The metal films have different thicknesses and coating sequences.After the growth, the Er3+and Tm3+profileswere analyzed by secondary ion mass spectrometry. The Er3+/Tm3+diffusivity and surface concentration were obtainedfrom the measured profiles. The diffusivity is influenced by neitherthe thickness nor the coating sequence of metal films. The solubilityconsists of Er3+and Tm3+components, and thetwo components equal the respective concentrations in the diffusionreservoir and change with the initial metal film thickness. Nevertheless,their sum, i.e., the solubility, remains a constant at a given temperatureand shows a weaker effect of either the crystal cut or the coatingsequence of Er and Tm films, together with the two components. Inaddition, the emission characteristics of the Er3+/Tm3+diffusion-codoped LN were investigated. The results showthat the codoping allows the combination of the wavelength emissionsof both ions, and the resultant emission band in the telecommunicationwindow around 1.5 μm is as wide as 150 nm, providing the possibilityof S+C+L broadband amplification by employing the commercial 980 and795 nm laser diodes as the pump sources. [ABSTRACT FROM AUTHOR]

Co-diffusion characteristics of Er3+ and Tm3+ ions in LiNbO3 crystal have been studied, together with two other properties: doping effect on refractive index of substrate, and Li out-diffusion. Er3+/ Tm3+-codoped LiNbO3 single-crystals were prepared by co-diffusion of stacked Er- and Tm-metal thin films, coated onto parts of the surfaces of X- and Z-cut congruent LiNbO3 crystal plates, at different temperatures and different durations in air. After diffusion, the surface refractive indices of the doped and undoped parts were measured by prism coupling technique, and the surface composition was evaluated from the measured indices. The results show that the dopings have negligible effect on the substrate index and the Li out-diffusion depends mainly on the diffusion temperature. The Er3+ and Tm3+ profiles were studied using secondary ion mass spectrometry, and a co-diffusion dynamical model is proposed and verified experimentally. From the measured profiles, the temperature-dependent Er3+/ Tm3+ diffusivity and solubility were obtained together with other relevant parameters, such as diffusion constant, activation energy, solubility constant and heat of solution. The Er3+ and Tm3+ co-diffusion exhibits similar temperature dependent diffusivity, and the dependence is similar to that of single-diffusion. In the co-diffusion case, the total solubility consists of two parts: Er3+ and Tm3+ parts, there is no anisotropy, and the value is equal to that of single-diffusion case, in which both ions have the similar solubility. The Er3+ and Tm3+ parts of solubility change relatively with the initial metal film thicknesses and hence have different temperature dependences. Nevertheless, their sum, i.e., the co-diffusion solubility, remains a constant at a given temperature. [ABSTRACT FROM AUTHOR]

Diffusion characteristics of Zr4+ in LiNbO3 single-crystal were studied. Zr4+-doped LiNbO3 crystal plates were prepared by in-diffusion of 100 nm thick ZrO2 film coated onto Z-cut congruent substrates in wet O2 at different temperatures. Zr4+-diffused profile was analyzed by secondary ion mass spectrometry. The results show that the Zr4+ diffusion follows the traditional diffusion theory. From the measured profiles, important diffusion parameters are obtained, such as diffusivity and its temperature dependence, diffusion constant, activation energy, surface concentration, and solubility. The Zr4+ has a diffusivity similar to that of Ti4+, implying that the Zr4+ doping and the Ti4+ diffusion can be performed simultaneously to simplify the fabrication process of a photorefractive-damage-resistant Zr4+-doped Ti-diffused LiNbO3 waveguide. [ABSTRACT FROM AUTHOR]

Diffusion-doping is an effective, practical method to improve material properties and widen material application. Here, we demonstrate a new physical phenomenon: diffusion control of an ion by another in LiNbO3 and LiTaO3 crystals. We exemplify Ti4+/Xn+ (Xn+ = Sc3+, Zr4+, Er3+) co-diffusion in the widely studied LiNbO3 and LiTaO3 crystals. Some Ti4+/Xn+-co-doped LiNbO3 and LiTaO3 plates were prepared by co-diffusion of stacked Ti-metal and Er-metal (Sc2O3 or ZrO2) films coated onto LiNbO3 or LiTaO3 substrates. The Ti4+/Xn+-co-diffusion characteristics were studied by secondary ion mass spectrometry. In the Xn+-only diffusion case, the Xn+ diffuses considerably slower than the Ti4+. In the Ti4+/Xn+ co-diffusion case, the faster Ti4+ controls the diffusion of the slower Xn+. The Xn+ diffusivity increases linearly with the initial Ti-metal thickness and the increase depends on the Xn+ species. The phenomenon is ascribed to the generation of additional defects induced by the diffusion of faster Ti4+ ions, which favors and assists the subsequent diffusion of slower Xn+ ion. For the diffusion system studied here, it can be utilized to substantially shorten device fabrication period, improve device performance and produce new materials. [ABSTRACT FROM AUTHOR]