23,733 research outputs found

    Observation of a cascaded process in intracavity terahertz optical parametric oscillators based on lithium niobate

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    Cascaded difference frequency generation has been observed in intracavity optical parametric oscillators based on bulk lithium niobate and producing nanosecond pulses of terahertz radiation. Two idler waves are generated, namely: the primary idler wave associated with the parametric down conversion process itself; and a secondary idler wave, due to difference frequency generation. Experimental investigations of the frequency, temporal evolution, propagation direction, intensity, phase matching and oscillation threshold of the generated down-converted waves are reported. The overall generation efficiency for the terahertz radiation is enhanced, thereby overcoming the Manley-Rowe limit. Advantages of the present approach over schemes based on periodically poled lithium niobate are identified.Publisher PDFPeer reviewe

    Subnanosecond GPS-based clock synchronization and precision deep-space tracking

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    Interferometric spacecraft tracking is accomplished by the Deep Space Network (DSN) by comparing the arrival time of electromagnetic spacecraft signals at ground antennas separated by baselines on the order of 8000 km. Clock synchronization errors within and between DSN stations directly impact the attainable tracking accuracy, with a 0.3-nsec error in clock synchronization resulting in an 11-nrad angular position error. This level of synchronization is currently achieved by observing a quasar which is angularly close to the spacecraft just after the spacecraft observations. By determining the differential arrival times of the random quasar signal at the stations, clock offsets and propagation delays within the atmosphere and within the DSN stations are calibrated. Recent developments in time transfer techniques may allow medium accuracy (50-100 nrad) spacecraft tracking without near-simultaneous quasar-based calibrations. Solutions are presented for a worldwide network of Global Positioning System (GPS) receivers in which the formal errors for DSN clock offset parameters are less than 0.5 nsec. Comparisons of clock rate offsets derived from GPS measurements and from very long baseline interferometry (VLBI), as well as the examination of clock closure, suggest that these formal errors are a realistic measure of GPS-based clock offset precision and accuracy. Incorporating GPS-based clock synchronization measurements into a spacecraft differential ranging system would allow tracking without near-simultaneous quasar observations. The impact on individual spacecraft navigation-error sources due to elimination of quasar-based calibrations is presented. System implementation, including calibration of station electronic delays, is discussed

    Vacuum-UV negative photoion spectroscopy of CH3F, CH3Cl and CH3Br

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    Using tunable vacuum-UV radiation from a synchrotron, negative ions are detected by quadrupolar mass spectrometry following photoexcitation of three gaseous halogenated methanes CH3_3X (X = F,Cl,Br). The anions X^-, H^-, CX^-, CHX^- and CH2_2X^- are observed, and their ion yields recorded in the range 8-35 eV. The anions show a linear dependence of signal with pressure, showing that they arise from unimolecular ion-pair dissociation, generically described as AB + hvv \rightarrow A^- + B+^+ (+ neutrals). Absolute cross sections for ion-pair formation are obtained by calibrating the signal intensities with those of F^- from both SF6_6 and CF4_4. The cross sections for formation of X^- + CH3_3+^+ are much greater than for formation of CH2_2X^- + H+^+. In common with many quadrupoles, the spectra of mm/zz 1 (H^-) anions show contributions from all anions, and only for CH3_3Br is it possible to perform the necessary subtraction to obtain the true H^- spectrum. The anion cross sections are normalised to vacuum-UV absorption cross sections to obtain quantum yields for their production. The appearance energies of X^- and CH2_2X^- are used to calculate upper limits to 298 K bond dissociation energies for Do^o (H3_3C-X) and Do^o (XH2_2C-H) which are consistent with literature values. The spectra suggest that most of the anions are formed indirectly by crossing of Rydberg states of the parent molecule onto an ion-pair continuum. The one exception is the lowest-energy peak of F^- from CH3_3F at 13.4 eV, where its width and lack of structure suggest it may correspond to a direct ion-pair transition

    Vacuum-UV negative photoion spectroscopy of CF3Cl, CF3Br and CF3I

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    Using synchrotron radiation negative ions have been detected by mass spectrometry following vacuum-UV photoexcitation of trifluorochloromethane (CF3_3Cl), trifluorobromomethane (CF3_3Br) and trifluoroiodomethane (CF3_3I). The anions F^-, X^-, F2_2^-, FX^-, CF^-, CF2_2^- and CF3_3^- were observed from all three molecules, where X = Cl, Br or I, and their ion yields recorded in the range 8-35 eV. With the exception of Br^- and I^-, the anions observed show a linear dependence of signal with pressure, showing that they arise from unimolecular ion-pair dissociation. Dissociative electron attachment, following photoionization of CF3_3Br and CF3_3I as the source of low-energy electrons, is shown to dominate the observed Br^- and I^- signals, respectively. Cross sections for ion-pair formation are put on to an absolute scale by calibrating the signal strengths with those of F^- from both SF6_6 and CF4_4. These anion cross sections are normalized to vacuum-UV absorption cross sections, where available, and the resulting quantum yields are reported. Anion appearance energies are used to calculate upper limits to 298 K bond dissociation energies for D0D^0(CF3_3-X) which are consistent with literature values. We report new data for D0D^0(CF2_2I^--F) ≤ 2.7 ± 0.2 eV and ΔfH2980\Delta_fH^0_{298} (CF2_2I+^+) ≤ (598 ± 22) kJ mol1^{-1}. No ion-pair formation is observed below the ionization energy of the parent molecule for CF3_3Cl and CF3_3Br, and only weak signals (in both I^- and F^-) are detected for CF3_3I. These observations suggest neutral photodissociation is the dominant exit channel to Rydberg state photoexcitation at these lower energies

    Inverse opal ceria–zirconia: architectural engineering for heterogeneous catalysis

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    The application of inverse opal structured materials is extended to the ceria–zirconia (Ce_(0.5)Zr_(0.5)O_2) system and the significance of material architecture on heterogeneous catalysis, specifically, chemical oxidation, is examined

    Unmasking quality: exploring meanings of health by doing art

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    This paper arises from a presentation at the ‘Quality in Healthcare’ symposium at Cumberland Lodge, England, in 2013. MK, CR and SH conceived the paper and led the writing of the manuscript. JF, JL-D, AC, DE contributed substantially to the intellectual content of the paper through providing critical commentary and interpretation. All authors read and approved the final manuscript

    Human Factors Engineering at Marshall Space Flight Center

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    The mission of NASA Marshall Space Flight Center (MSFC) is to develop, implement, and maintain systems for space transportation and microgravity research. Factors impacting the MSFC position as a leader in advancing science and technology include: (1) heightened emphasis on safety; (2) increased interest in effective resource utilization; and (3) growing importance of employing systems and procedures that pragmatically support mission science. In light of these factors, MSFC is integrating human factors engineering (HFE) into the systems engineering process. This paper describes the HFE program, applications of HFE in MSFC projects, and the future of HFE at MSFC
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