241 research outputs found

    Modulation Response of Twin Optically Coupled Diode Lasers

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    Diode lasers are useful in military and commercial applications that have strict requirements for size, weight and power. This includes the use of diode lasers in optoelectronic and photonic integrated circuits, which can lead to new technologies in optical communications and optical interconnects in high performance computing systems. For these systems to be effective, the diode laser must be modulated at frequencies beyond current limits which are typically a few GHz. This barrier can be broken by optically coupling a diode laser with a similar laser. A set of single mode rate equations models the dynamics of twin optically coupled diode lasers. Steady states of the system are derived analytically or calculated numerically when an analytic expression is not easily available. The stability of the steady states is examined by using a linear stability analysis, which is also used in an algorithm that calculates the infinitesimal modulation response. The modulation response is also calculated by using a numerical method that directly integrates the rate equations. Typical parameters for an InGaAsP diode laser are used in the algorithms to investigate mutual coupling and evanescent coupling. It will be shown that mutually coupled lasers can be effectively modulated out to frequencies of approximately 9 GHz compared to 4 GHz for a solitary laser. For evanescent coupling, the steady states are unstable over large regions of the parameter space, but this is remedied by introducing asymmetric DC currents through the lasers or by introducing the effects of gain saturation. With stable steady states, evanescently coupled lasers can be effectively modulated at frequencies out to about 30 GHz which is more than a seven fold improvement over a solitary laser

    Hyperfine Interactions in the Electron Paramagnetic Resonance Spectra of Point Defects in Wide-Band-Gap Semiconductors

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    The focus of this research was to acquire definitive experimental data on predominant point defects in three important wide-band-gap semiconductors. Hyperfine interactions in electron paramagnetic resonance spectra were used to characterize the neutral nitrogen acceptor in zinc oxide, to identify a silicon interstitial impurity in titanium dioxide, and to determine the electronic structure of the singly ionized sulfur vacancy in stannous hexathiohypodiphosphate (SPS). Research on the basic properties of these technologically important materials plays a crucial role in the development of advanced optical and electronic systems. Zinc oxide is an electro-optic material with the potential to produce high performance electronics and also ultraviolet detectors and emitters. The angular dependencies of axial and basal 67Zn hyperfine lines were used to extract 67Zn hyperfine interaction parameters for the neutral nitrogen acceptor in zinc oxide. These data establish the exact nature of the ground-state wave function associated with this important acceptor. The experimental information obtained in this study about the ground-state wave function will allow computational theorists to model the nitrogen acceptor and determine whether it can successfully lead to p-type conduction in zinc oxide. The search for p-type zinc oxide is one of the most important basic questions in present-day research on wide-band-gap semiconductors

    Neutral Nitrogen Acceptors in ZnO: The \u3csup\u3e67\u3c/sup\u3eZn Hyperfine Interactions

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    Electron paramagnetic resonance (EPR) is used to characterize the 67Zn hyperfine interactions associated with neutral nitrogen acceptors in zinc oxide. Data are obtained from an n-type bulk crystal grown by the seeded chemical vapor transport method. Singly ionized nitrogen acceptors (N−) initially present in the crystal are converted to their paramagnetic neutral charge state (N0) during exposure at low temperature to 442 or 633 nm laser light. The EPR signals from these N0 acceptors are best observed near 5 K. Nitrogen substitutes for oxygen ions and has four nearest-neighbor cations. The zinc ion along the [0001] direction is referred to as an axial neighbor and the three equivalent zinc ions in the basal plane are referred to as nonaxial neighbors. For axial neighbors, the 67Zn hyperfine parameters are A‖ = 37.0 MHz and A⊥ = 8.4 MHz with the unique direction being [0001]. For nonaxial neighbors, the 67Zn parameters are A1 = 14.5 MHz, A2 = 18.3 MHz, and A3 = 20.5 MHz with A3 along a [10ˉ10] direction (i.e., in the basal plane toward the nitrogen) and A2 along the [0001] direction. These 67Zn results and the related 14N hyperfine parameters provide information about the distribution of unpaired spin density at substitutional neutral nitrogen acceptors in ZnO

    Interstitial Silicon Ions in Rutile TiO\u3csub\u3e2\u3c/sub\u3e Crystals

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    Electron paramagnetic resonance (EPR) is used to identify a new and unique photoactive silicon-related point defect in single crystals of rutile TiO2. The importance of this defect lies in its assignment to interstitial silicon ions and the unexpected establishment of silicon impurities as a major hole trap in TiO2. Principal g values of this new S=1/2 center are 1.9159, 1.9377, and 1.9668 with principal axes along the [¯110],[001], and [110] directions, respectively. Hyperfine structure in the EPR spectrum shows the unpaired spin interacting equally with two Ti nuclei and unequally with two Si nuclei. These silicon ions are present in the TiO2 crystals as unintentional impurities. Principal values for the larger of the two Si hyperfine interactions are 91.4, 95.4, and 316.4 MHz with principal axes also along the [¯110],[001], and [110] directions. The model for the defect consists of two adjacent Si ions, one at a tetrahedral interstitial site and the other occupying a Ti site. Together, they form a neutral nonparamagnetic [Siint−SiTi]0 complex. When a crystal is illuminated below 40 K with 442-nm laser light, holes are trapped by these silicon complexes and form paramagnetic [Siint−SiTi]+ defects, while electrons are trapped at oxygen vacancies. Thermal anneal results show that the [Siint−SiTi]+ EPR signal disappears in two steps, coinciding with the release of electrons from neutral oxygen vacancies and singly ionized oxygen vacancies. These released electrons recombine with the holes trapped at the silicon complexes

    Copper Doping of ZnO Crystals by Transmutation of \u3csup\u3e64\u3c/sup\u3eZn to \u3csup\u3e65\u3c/sup\u3eCu: An Electron Paramagnetic Resonance and Gamma Spectroscopy Study

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    Transmutation of 64Zn to 65Cu has been observed in a ZnO crystal irradiated with neutrons. The crystal was characterized with electron paramagnetic resonance (EPR) before and after the irradiation and with gamma spectroscopy after the irradiation. Major features in the gamma spectrum of the neutron-irradiated crystal included the primary 1115.5 keV gamma ray from the 65Zn decay and the positron annihilation peak at 511 keV. Their presence confirmed the successful transmutation of 64Zn nuclei to 65Cu. Additional direct evidence for transmutation was obtained from the EPR of Cu2+ ions (where 63Cu and 65Cu hyperfine lines are easily resolved). A spectrum from isolated Cu2+ (3d9) ions acquired after the neutron irradiation showed only hyperfine lines from 65Cu nuclei. The absence of 63Cu lines in this Cu2+ spectrum left no doubt that the observed 65Cu signals were due to transmuted 65Cu nuclei created as a result of the neutron irradiation. Small concentrations of copper, in the form of Cu+-H complexes, were inadvertently present in our as-grown ZnO crystal. These Cu+-H complexes are not affected by the neutron irradiation, but they dissociate when a crystal is heated to 900 °C. This behavior allowed EPR to distinguish between the copper initially in the crystal and the copper subsequently produced by the neutron irradiation. In addition to transmutation, a second major effect of the neutron irradiation was the formation of zinc and oxygen vacancies by displacement. These vacancies were observed with EPR

    New challenges in studying nutrition-disease interactions in the developing world.

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    Latest estimates indicate that nutritional deficiencies account for 3 million child deaths each year in less-developed countries. Targeted nutritional interventions could therefore save millions of lives. However, such interventions require careful optimization to maximize benefit and avoid harm. Progress toward designing effective life-saving interventions is currently hampered by some serious gaps in our understanding of nutrient metabolism in humans. In this Personal Perspective, we highlight some of these gaps and make some proposals as to how improved research methods and technologies can be brought to bear on the problems of undernourished children in the developing world

    Identification of the Zinc-oxygen Divacancy in ZnO Crystals

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    An electron paramagnetic resonance (EPR) spectrum in neutron-irradiated ZnO crystals is assigned to the zinc-oxygen divacancy. These divacancies are observed in the bulk of both hydrothermally grown and seeded-chemical-vapor-transport-grown crystals after irradiations with fast neutrons. Neutral nonparamagnetic complexes consisting of adjacent zinc and oxygen vacancies are formed during the irradiation. Subsequent illumination below ∼150 K with 442 nm laser light converts these (V2−Zn − V2+O)0 defects to their EPR-active state (V−Zn − V2+O)+ as electrons are transferred to donors. The resulting photoinduced S = 1/2 spectrum of the divacancy is holelike and has a well-resolved angular dependence from which a complete g matrix is obtained. Principal values of the g matrix are 2.00796, 2.00480, and 2.00244. The unpaired spin resides primarily on one of the three remaining oxygen ions immediately adjacent to the zinc vacancy, thus making the electronic structure of the (V−Zn − V2+O)+ ground state similar to the isolated singly ionized axial zinc vacancy. The neutral (V2−Zn − V2+O)0 divacancies dissociate when the ZnO crystals are heated above 250 °C. After heating above this temperature, the divacancy EPR signal cannot be regenerated at low temperature with light

    Sn Vacancies in Photorefractive Sn\u3csub\u3e2\u3c/sub\u3eP\u3csub\u3e2\u3c/sub\u3eS\u3csub\u3e6\u3c/sub\u3e Crystals: An Electron Paramagnetic Resonance Study of an Optically Active Hole Trap

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    Electron paramagnetic resonance (EPR) is used to identify the singly ionized charge state of the Sn vacancy (V−Sn) in single crystals of Sn2P2S6 (often referred to as SPS). These vacancies, acting as a hole trap, are expected to be important participants in the photorefractive effect observed in undoped SPS crystals. In as-grown crystals, the Sn vacancies are doubly ionized (V2−Sn) with no unpaired spins. They are then converted to a stable EPR-active state when an electron is removed (i.e., a hole is trapped) during an illumination below 100 K with 633 nm laser light. The resulting EPR spectrum has g-matrix principal values of 2.0079, 2.0231, and 1.9717. There are resolved hyperfine interactions with two P neighbors and one Sn neighbor. The isotropic portions of these hyperfine matrices are 167 and 79 MHz for the two 31P neighbors and 8504 MHz for the one Sn neighbor (this latter value is the average for 117Sn and 119Sn). These V−Sn vacancies are shallow acceptors with the hole occupying a diffuse wave function that overlaps the neighboring Sn2+ ion and (P2S6)4− anionic unit. Using a general-order kinetics approach, an analysis of isothermal decay curves of the V−Sn EPR spectrum in the 107–115 K region gives an activation energy of 283 meV

    Sulfur Vacancies in Photorefractive Sn\u3csub\u3e2\u3c/sub\u3eP\u3csub\u3e2\u3c/sub\u3eS\u3csub\u3e6\u3c/sub\u3e Crystals

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    A photoinduced electron paramagnetic resonance (EPR) spectrum in single crystals of Sn2P2S6 (SPS) is assigned to an electron trapped at a sulfur vacancy. These vacancies are unintentionally present in undoped SPS crystals and are expected to play an important role in the photorefractive behavior of the material. Nonparamagnetic sulfur vacancies are formed during the initial growth of the crystal. Subsequent illumination below 100 K with 442 nm laser light easily converts these vacancies to EPR-active defects. The resulting S = 1/2 spectrum shows well-resolved and nearly isotropic hyperfine interactions with two P ions and two Sn ions. Partially resolved interactions with four additional neighboring Sn ions are also observed. Principal values of the g matrix are 1.9700, 1.8946, and 1.9006, with the corresponding principal axes along the a, b, and c directions in the crystal. The isotropic parts of the two primary 31P hyperfine interactions are 19.5 and 32.6 MHz and the isotropic parts of the two primary Sn hyperfine interactions are 860 and 1320 MHz (the latter values are each an average for 117Sn and 119Sn). These hyperfine results suggest that singly ionized sulfur vacancies have a diffuse wave function in SPS crystals, and thus are shallow donors. Before illumination, sulfur vacancies are in the doubly ionized charge state because of compensation by unidentified acceptors. They then trap an electron during illumination. The EPR spectrum from the sulfur vacancy is destroyed when a crystal is heated above 120 K in the dark and reappears when the crystal is illuminated again at low temperature
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