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    Semiclassical theory of proton transport in ice
    (1967-04) Kim, Dong-Yun; Schmidt, V. Hugo
    A method is described for calculating proton or other ion mobility which is applicable if mobility is limited by lattice scattering rather than by barrier jumping. The Boltzmann transport equation is used, with the collision term calculated from the electrostatic interactions between the mobile ion and the vibrating lattice. In particular the proton mobility in ice is calculated. The lattice vibrations are approximated by a Debye spectrum for translational vibrations of water molecules, plus an Einstein spectrum for modes in which protons vibrate almost as independent particles. Scattering by phonons somewhat below the Debye cutoff frequency is of the greatest importance in determining the mobility, and the proton modes have negligible effect. The calculated mobility agrees reasonably well with the experimental value.
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    Simple coulometer for studying protonic conduction in crystals
    (1965-12) Schmidt, V. Hugo
    NOTES ON EXPERIMENTAL TECHNIQUE AND APPARATUS A simple glass coulometer with mercury electrodes was designed to measure the amount of gas evolved upon passing current through single crystals, to determine the extent to which electrical conduction in these crystals is due to protons or other gas-forming ions. It is useful if at least one coulomb can be passed through the crystal in a reasonable time interval. With single crystals of KH2PO4 and Li(N2H5)SO4 in this coulometer, the ratio of hydrogen evolution rate to crystal current indicates entirely protonic conduction.
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    Deuteron NMR Study of Lithium Hydrazinium Sulfate
    (1969-09) Howell, Francis L.; Schmidt, V. Hugo
    The magnetic resonance spectrum of the deuterons in single crystals of LiN2D5SO4 has been studied between 78 and 458°K. The electric quadrupole coupling constants, the asymmetry parameters, and the orientations of the electric field gradient (efg) tensors relative to the crystal axes were obtained at 78°K, 193°K, 25°C, 65°C, and 95°C. The orientations of the efg tensors are considered in relation to nearby atomic sites. At 78°K the spectrum contains distinct lines due to the five deuterons of the N2D5 + ion. Between 110 and 150°K the lines due to the three deuterons of the ND3 group broaden and merge to a single pair which is still visible at 185°C. A small change with temperature in the coupling constant associated with this pair of lines is discussed. The lines due to the two deuterons of the ND2 group broaden and merge to a single pair between 0 and 50°C. These line mergers result from hindered rotation of the ND2 and ND3 groups. Estimates of the activation energies for these motions are made. These changes in the spectrum are related to the results of earlier NMR studies and to previous electrical conductivity and dielectric constant measurements.
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    Ferroelectricity Experiment for Advanced Laboratory
    (American Institute of Physics, 1969-04) Schmidt, V. Hugo
    An experiment suitable for a junior or senior physics laboratory is described, in which the spontaneous polarization and coercive field for Rochelle salt are measured from the ferroelectric hysteresis loops, over the temperature range −18° to +24°C in which this crystal is ferroelectric. The suitability of triglycine sulfate for this experiment is discussed. The apparatus is also useful in demonstrating the relation of capacitance to electrode geometry, and in determining dielectric constants.
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    Observation of the 169Tm and 27Al NMR in Thulium Aluminum Garnet
    (American Institute of Physics, 1969-03) Jones, E. D.; Schmidt, V. Hugo
    The observations of the 169Tm and 27Al nuclear magnetic resonances(NMR) in a single crystal of cubic thuliumaluminumgarnet are reported. The 27Al MNR was studied between 1.5° and 300°K, while the 169Tm NMR was observed only for T<4°K. From a study of the angular dependences of the 169Tm NMR fields, the (ξ, η, ζ) components of the Tm3+ susceptibility tensor were found to be highly ansiotropic and in units of emu/gram‐atom, χ1=0.014, χ2=0.551, and χ3=0.03. The room temperature 27Al nuclear quadrupolar coupling constants e 2 qQ/h for the a and d sites were measured to be (0.892±0.005) and (6.155±0.005) MHz, respectively. The 27AlNMR frequency shifts for both sites were found to be angular and temperature dependent. A calculation for the observed angular dependences of the 27AlNMR frequency shifts in terms of dipolar fields is found to give reasonable agreement with experiment for the 1.5° and 300°K NMR data.
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    Dynamical Effects of Deuteron Intrabond Jumping in KD2PO4
    (American Physical Society, 1967-12) Schmidt, V. Hugo
    Deuteron jumps along hydrogen bonds in KD2PO4 associated with effective motion of Slater-Takagi DPO4 and D3PO4 groups are related to the deuteron magnetic-resonance spectrum and relaxation both above and below the ferroelectric transition temperature Tc, and to the dielectric relaxation and the domain-wall mobility. Below Tc the deuterons assume ordered bond positions, but occasionally jump to the opposite positions. The correlation time for the electric-field-gradient fluctuations seen by a deuteron undergoing such motion is found to be short above Tc and even shorter below Tc. The rms amplitude of the fluctuations drops rapidly below Tc. These results are used to explain the temperature dependence of the splitting and lack of line broadening in the deuteron spectrum below Tc, and the rapid decrease of the spin-lattice transition probabilities below Tc. Relaxation data above Tc, which yielded the energies and fractional populations of DPO4 and D3PO4 groups, are reanalyzed using the recently reported field-gradient tensors at the two bond positions. The dielectric relaxation is calculated, and good agreement with the high dielectric loss measured at microwave frequencies is found. The jump time for a DPO4 or D3PO4 group is found to be near hkT, implying little correlation between successive jumps, in contrast to KH2PO4. This jump time is used in a calculation of domain-wall mobility in KD2PO4.
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    Sensitive Low Level Transistorized NMR Spectrometer Employing Frequency Modulation
    (American Institute of Physics, 1966-08) Blankenburg, Fred; Knispel, Roy; Schmidt, V. Hugo
    A transistorized NMR spectrometer has been developed which affords sensitivity comparable to that of the best vacuum tube spectrometers. This spectrometer has operated with sample coil voltages below 10 mV peak‐to‐peak. Frequency modulation is used to facilitate modulation at frequencies high enough to minimize effects of transistor 1/fnoise.
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    Deuteron Intrabond Motion and Ferroelectricity in KD2PO4
    (American Physical Society, 1964-01) Silsbee, Henry; Uehling, Edwin A.; Schmidt, V. Hugo
    The Slater theory of the ferroelectric phase transition in KH2PO4 type crystals as modified by Takagi and extended by Senko is examined again in the light of recent measurements of parameters made on KD2PO4. Making full use of the measurements, and assigning an appropriate numerical value to one adjustable parameter which is not independently measured, the theory gives a nearly correct description of the shape of the spontaneous polarization curve. Also the value obtained for the Curie constant is probably satisfactory in view of limitations of the model and uncertainty of the high-temperature experimental data. The theory fails, however, in at least one important respect; the transition entropy is overestimated. This and other discrepancies are discussed briefly.
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    Electrical Conductivity of (NH4)2SO4 Single Crystals
    (American Institute of Physics, 1963-06) Schmidt, V. Hugo
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    Random Motion of Deuterons in KD2PO4
    (American Physical Society, 1969-04) Schmidt, V. Hugo; Uehling, Edwin A.
    Magnetic resonance studies of the deuteron in KD2PO4 have been conducted which show the existence of deuteron jumping between and within hydrogen bonds. The experimental results help to explain electrical conductivity and ferroelectric phenomena in crystals of this type. Pulse magnetic resonance experiments show that the lifetime TXY against deuteron jumping between X- and Y-oriented hydrogen bonds is 15 msec at 70°C with a jump activation energy of approximately 0.58 ev. The c-axis electrical conductivity of KD2PO4 is found to have the same activation energy, with a value of 1.16×10−10 (ohmcm)−1 at 25°C. The Δm=1(P1) and Δm=2(P2) deuteron spin-lattice relaxation transition probabilities due to X−Y jumps have been calculated from the known values of TXY and the electric field gradient tensors at X and Y deuteron sites. Their magnitudes and the dependences of these magnitudes on magnetic field, temperature, and orientation are in good agreement with experiment. Further measurements of P1 and P2 separately give a component of transition probability proportional to exp(0.078 ev/kT) and independent of magnetic field. The orientation dependences of P1 and P2 for this component indicate quadrupolar relaxation due to deuteron jumps along hydrogen bonds, with a jump time of order 10−11 sec at 215°K. The existence of intrabond jumps governed by an activation energy is shown to be consistent with the Slater theory of KH2PO4 as modified by Takagi.
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