Ultrasonic determination of electron-phonon scattering rates in copper

Electron-phonon scattering rates in ultrapure single crystals of copper have been determined from the temperature dependence of the magnetoacoustic oscillation amplitudes for various orbits on the Fermi surface using both longitudinal and transverse waves. The central belly orbit seattering rate is found to be (6.0±0.3)×10⁶ T ³ sec^?1. Additionally, a rate of (2.9±0.2)×10⁶ T ³ sec^?1 is found which is attributed to belly orbits displaced from the zone center by about 1.25/a ₀, wherea ₀ is the lattice constant. Geometric oscillations associated with the [111]—directed open orbit are observed at low fields forq‖ [113] and the rate for this orbit is found to be (4.8±0.3)×10⁶ T ³ sec^?1. Geometric oscillations for the dog's bone and neck orbits are observable but rates for these orbits are believed to be unreliable. Our measured rates are compared with those of other workers.     

Observation of muonic HF molecule formation with TF μ− SR

Negative muon polarization has been measured in pure gaseous Ne (24 atm) and in Ne+H₂ mixtures (24 atm Ne+1.8 atm H₂, 8 atm H₂ and 16 atm H₂). The experiment was performed at JINR (Dubna) on aSR-spectrometer [1] with 200 G transverse magnetic field at room temperature. In pure Ne no polarization was observed (a ₀=0.09±0.1%) while in Ne+H₂ mixtures clear precession signals were detected at the free-muon frequency with asymmetries a_1.8=0.33±0.13%,a ₈=0.33±0.14% anda ₁₆=0.59±0.09%. The fact that polarization appears in the muonic HF molecule shows that at the moment of the molecule formation (t10^–10 s) the muon is not completely depolarized. The estimate of the reaction constantk=(2.3±1.6)×10^–11cm³ s^–1 agrees with the experimental values obtained by other methods. The result achieved demonstrates that ^– SR-method can be applied for studying fast kinetics processes in the gas phase and in particular for measuring chemical reaction rates of halogen atoms and ions.     

Diffusion of selenium and tellurium in silicon

Diffusion of selenium and tellurium in silicon has been investigated in the temperature range 1000°C to 1310°C by sheet conductivity. For SiSeD ₀= 0.3±0.1 cm²/s andh=2.6±0.1 eV, and for SiTeD ₀=0.9±0.3 cm²/s and h=3.3±0.1eV have been obtained. The surface concentrations for both dopants were of the order of 5 × 10¹³ to 6×10¹⁶cm^–3. The Hall coefficient leads to an energy level of 300±15meV for selenium and 200±20meV for tellurium.     

Inclusive production of φ-mesons in neutron-proton interaction at 30–70 GeV/c

A signal of the-K⁺K^– decays has been observed in neutron-hydrogen interactions at energies of 30–70 GeV in an experiment using the BIS-2 spectrometer. The longitudinal momentum spectrum in the forward region,x _F<0·1 atp _T<1 GeV/c, can be well described by a power law dependence (1–x _F)^N withN=4·28±0·42. Thep _T ² -spectrum has been parametrized by the exp(–Bp _T ² ) law with the exponentB=(3·02±0·55) (GeV/c)^–2. The extrapolation of the measured cross section to the full kinematic region yields a value of (220±85) b in agreement with measurements from the proton beams.     

Nonlinear Optical Characteristics of BSO and BGO Photorefractive Crystals in Visible and Infrared Ranges

Nonlinear refraction, nonlinear absorption and optical limiting in photorefractive crystals Bi₁₂SiO₂₀(BSO) and Bi₁₂GeO₂₀(BGO) at the wavelengths of 1064 and 532 nm were investigated. It was shown that both BSO and BGO crystals possess by positive nonlinear refraction in two investigated spectral ranges (n ₂ ^BSO=(2.5 ± 0.5)× 10^–12 esu, n ₂ ^BGO=(6.3 ± 1.3)× 10^–12 esu at equals 1064 nm; n ₂ ^BSO=(4.4 plusmn; 0.9)× 10^–12 esu, n ₂ ^BGO=(7.4 ± 1.5)× 10^–12 esu at = 532 nm). The nonlinear absorption was due to three-photon absorption at the wavelength of 1064 nm ( ⁽³⁾ _BSO=(2.5 ± 0.8)× 10^–20cm³W^–2, ⁽³⁾ _BSO=(4.4 ± 1.3)× 10^–20cm³W^–2) and two-photon absorption at the wavelength of 532 nm ( ⁽²⁾ _BSO=(2 ± 0.4)× 10^–9cm W^–1, ⁽²⁾ _BGO=(3.7 ± 0.7)× 10^–9cm W^–1).     

The dependence of the neutron temperature on the geometric parameter for water and loose diphenyl

The dependence of the neutron temperatureT _n on the geometric parameterB ² was measured by the pulse method in water and loose diphenyl. The measurements were made on a moderator poisoned by cadmium sulphate, a substance whose absorption cross-section is non 1/v.The following results were obtained: For waterT _n [eV]=–(0·00391±0·00045)B ² [cm^–2]+(0·02537±0·00035) for loose diphenyl:T _n [eV]=–(0·01014±0·00152)B ² [cm^–2]+(0·02518±0·00054).We are indebted to J. Jirou and J. Jadavan for their assistance in the measurements, the accelerator operation and electronic apparatus maintenance.     

Influence of Vibrational Excitation of Triplet Molecules of Anthraquinone on the Photochemical Processes in Gas Mixtures with Amines

By the quenching of the delayed fluorescence (DF) of anthraquinone vapors by aliphatic amines (diethylamine, dibutylamine, cyclohexylamine) and pyridine the photoinduced processes proceeding with the participation of vibrationally excited triplet molecules of anthraquinone have been investigated. The DF quenchingrate constants K _q varying from 1·10⁶ sec^–1·torr^–1 in mixtures with diethylamine to 7·10³ sec^–1·torr^–1 in mixtures with pyridine have been estimated. A correlation between the values of K _q and the ionization potentials of foreign gases confirming the important role of interactions with charge transfer in the quenching of triplet molecules in the gas phase has been established. The influence of other relaxation processes on the DF quenching is considered. It is shown that the intermolecular vibrational relaxation in the T ₁ triplet state leading to the establishment of relaxation equilibrium at a vibrational temperature T _vib considerably increasing the medium temperature is the fastest process among the biomolecular processes (rate constants K _col ^V > 10⁶ sec^–1·torr^–1 > K _q). The values of T _vib and the vibrational energies E _vib of the triplet molecules after the energy exchange in the collisional complex have been estimated. It has been concluded that the photochemical reaction yield is determined by the intermolecular processes proceeding in the T ₁ state at a vibrational equilibrium characterized by high values of T _vib. The influence of E _vib of triplet molecules on the DF quenching rates at a photoinduced electron transfer is considered.     

Volume and grain boundary diffusion of implanted 113Sn in aluminium

Volume and grain boundary diffusion of ¹¹³Sn in aluminium was investigated with the radiotracer method. The implantation technique was used for tracer deposition to avoid problems of tracer hold-up caused by the oxide layer always present on aluminium. The diffusion penetration was chosen large enough to permit serial sectioning of samples with the aid of a microtome.The temperature dependence of the volume diffusivity was determined as D(T)=4.54×10^–5×exp[–(114.5±1.2)kJmol^–1/RT] m ² s ^–1. This confirms previous measurements from our group which already showed that Sn is the fastest foreign metal diffusor so far investigated in aluminium.Grain boundary diffusion of ¹¹³Sn in Al polycrystals was measured in the type-B kinetic regime. The grain boundary diffusion product P=sD _gb (s=segregation factor, =grain boundary width, D _gb=grain boundary diffusivity) was found to be strongly affected by the impurity content of aluminium. For Al polycrystals of 99.9992% nominal purity we obtained P _5N(T)=1.08×10^–8exp [–(96.9±7.5) kJ mol^–1/RT] m³ s^–1 and for less pure Al polycrystals of 99.99% nominal purity P _4N(T)=3.0×10^–10 exp [–(90.1±4.2) kJ mol^–1/RT] m³ s^–1 was determined. The grain boundary diffusion product in the purer material is more than one order of magnitude higher than in the less pure material. Very likely this is an effect of co-segregation of non-diffusant impurities into the grain boundaries.     

The temperatures of protons andπ − mesons in central nucleus-nucleus interactions at a momentum of 4.5 GeV/c per incident nucleon

An estimate of the temperature of protons and ^– mesons in central He–Li, He–C, C–C, C–Ne, C–Cu, C–Pb, O–Pb, Mg–Mg interactions is presented. The results indicate an increase of the proton temperature with increasing mass numbers of projectile and target nuclei (A _p ,A _T ) fromT _p =(118±3) MeV for He–Li toT _p =(141±2) MeV for C–Pb. The temperature of ^– mesons does not depend onA _P ,A _T andT 95 MeV. A satisfactory fit for ^– mesons in C–Cu, C–Pb, O–Pb, Mg–Mg collisions can be achieved by using a form involving two temperatures,T ₁ andT ₂. The relative yield of the high temperature component (T ₂) is 24% for C–Cu, C–Pb, and Mg–Mg interactions. The observed results forT _P in C–Ne, C–Cu and C–Pb collisions are consistent with the prediction of the thermodynamic hagedorn model.     

Experimental determination of the rates of the excited muonic hydrogen charge exchange on helium

The data of the experiment with the H₂+⁴He mixture are analyzed in order to estimate muon transfer rates from the excited states of p atoms to helium. Experimental data turned out to be insensible to the transfer rates from the metastable 2s state. The rates forn=3, 4, 5 were found to be: ⁽³⁾=(2±7)×10¹⁰ s^–1, ⁽⁴⁾=(16±13)×10¹¹ s^–1, ⁽⁵⁾=(75±60) ×10¹¹ s^–1, respectively.     

Decay of Hf172

The internal conversion spectrum of Hf¹⁷² was examined with an intermediate image magnetic spectrometer. The gamma-ray spectrum and gamma-gamma coincidence spectrum were studied by means of scintillation spectrometers. The half-life of the 65·9 keV excited level in Lu¹⁷² was found to beT _1/2 = (3·32±0·20) × 10^–7 sec. The proposed decay scheme is discussed.On the same apparatus the half-life of the 206·25 keV excited level in Re¹⁸⁷ was measured and the result isT _1/2 = (5·05±0·13) × 10^–7 sec.The authors wish to thank to Ing. Vobecký and Ing. Matalka for the separation of Hf and Z. Praáková for assistance in the numerical calculation.     

Absolute concentration measurements of C2 in a diamond CVD reactor by laser-induced fluorescence

By use of Laser-Induced Fluorescence (LIF) the absolute concentration of the C₂ radical in a microwave excited diamond chemical vapour deposition plasma has been measured for the first time. LIF spectra of thed ³ _g–a ³ _u (1,0) Swan band near 473 nm were recorded and synthesized theoretically allowing the plasma temperature of 2100 ± 200 K to be inferred. Quenching rates were determined from time-resolved measurements of the fluorescence decay. By calibrating the LIF detection system, using spontaneous Raman scattering in H₂ in the reactor vessel, the absolute concentration of C₂ was determined to be (7.5 ± 1.7) × 10¹⁰ cm^–3. Observations of the C₂ density under varying plasma conditions are reported.     

Structural phase transition and internal fields in rubidium thiocyanate probed through vibrational spectroscopy

A comprehensive vibrational study of Rubidium thiocyanate (RbNCS), in the 298–448°K range reveals that the orthorhombic to tetragonal transition atT _c440°K is of order-disorder type exhibiting purely second order characteristics. A consistent order-parameter exponent 0.45±0.04 has been obtained from both Raman and IR measurements. In the Raman spectra, the appearance of sidebands in both the C–N&C–S stretching modes and their temperature dependence indicate the existence and a gradual diminution of internal electric field asT approachesT _c. These results have been discussed in the context of an anharmonic oscillator model. An activation energy (U) for the reorientational motion of NCS^– ions,U0.29±0.02 eV, has been calculated from large changes in the bandwidth (_C-N) nearT _c.     

Ab Initio Study of the Phosphorescence of Nitrite Ions

In order to interpret the phosphorescence spectra of NaNO₂ and similar single crystals, we performed MCSCF geometry optimization in the ground singlet (X ¹ A ₁) and in the first excited triplet (a ³ B ₁) states of the NO ₂ ^- ion and MCSCF quadratic response (QR) calculation of the a ³ B ₁–X ¹ A ₁ transition probability at different bending angles and asymmetric stretch modes. The complete form of the spin–orbit coupling (SOC) operator is accounted for in the QR procedure. Dunning's correlation-consistent polarized valence double- (cc-pVDZ) and triple- (cc-pVTZ) basis sets are imployed. The electric-dipole transition moment from the T ^z spin sublevel (z is the C ₂ axis) oriented along the y direction (the other in-plane axis) is found to be 5 times higher than that from the T ^y sublevel in the ground-state geometry. This is in agreement with polarization measurements and with optical detection of ESR spectra. The T ^z–S ₀ transition moment decreases almost linearly with an increase in the ONO bond angle. The so-called non-Condon effects in the phosphorescence spectra of NaNO₂ crystals are explained on these backgrounds. The long progression of the bending vibrations (v ₂, a ₁) with an anomolous intensity distribution in the T ^z–S ₀ transition and additional involvement of the asymmetric stretch mode (v ₃, b ₂) in the T ^y–S ₀ transition are interpreted by force field and SOC calculations in the MCSCF-response technique. Configuration interaction (CI) calculations of the spin-allowed electric dipole transitions in NO ₂ ^- ions with effective one-electron SOC operator matrix element estimations were done for comparison with the results of the quadratic and linear response methods. Other T _n–S ₀ transitions are also studied. Finally, a short discussion of nonradiative processes is presented.     

Saturation of ionization edge absorption by donors in germanium

A study of saturation of the absorption and photoconductivity of Sb and P donors in Ge for radiation of 90 m wavelength, i.e., of energy very closely above their ionization edges is presented at T=9.3 K. Under these conditions negligible heating by the excess radiation energy is expected, which provides a convenient opportunity to study the kinetics of photoionization and recombination. From these measurements we have determined the donor capture cross section of electrons at 9.3 K to be _c=(1.2±0.7)×10^–12cm^–2, and the relaxation time from the 2s to the ground state as ₂₁=(5.8±1.0)×10^–10s. The saturation intensity of the absorption coefficient is around three orders of magnitude higher than the saturation intensity of the photoconductivity. We explain the nonlinear photoconductivity by the Debye-Conwell dependence of the mobility on the number of photoionized donors and compensating acceptors.     

Rate of abstraction of hydrogen atoms from ethane by muonium

Thermal reaction rates for the gas-phase reaction Mu+C₂H₆MuH+C₂H₅ have been measured bySR over the temperature range 510–730 K. The usual Arrhenius expression,k=Aexp(–E _a /RT), fits the data well, giving parametersA=1.0×10^–9 cm³ molecule^–1 s^–1 andE _a =15.35 kcal/mol. The activation energyE _a is 5.5 kcal/mol higher than for the H atom variant of this reaction, indicating a marked difference in reaction dynamics. Preliminary analysis indicates a still greater difference between Mu and H for the corresponding CH₄ reaction.     

Isomeric transitions between shape coexisting states in iodine isotopes withA=115, 119 and 121

Applying delayed- r.f. coincidences and generalized centroid-shift analysis, nanosecond isomers in some odd-A iodine isotopes are studied in-beam. The reactions¹⁰⁶Cd(¹²C,p2n) and^116,118Sn(⁶Li,3n) have been used. The following half-lives were determined:T _1/2(565 keV)=0.50±0.10 ns andT _1/2(837 keV) =0.90±0.20 ns in¹¹⁵I,T _1/2(687 keV)=5.50±0.50 ns andT _1/2(2418 keV)=4.0±0.50 ns in¹¹⁹I as well asT _1/2(812 keV)=0.35±0.20 ns andT _1/2(445 keV)<0.10 ns=">¹²¹I. A systematics of the absolute probabilities for the transitions deexciting theg _9/2 9/2⁺ and _11/2 11/2 ₁ ^– band heads in^115–125I is presented and discussed.Partly supported by the Bulgarian National Research Foundation under contracts PH14, and PH31 and Kernforschungszentrum Karlsruhe, Stabsabteilung Internationale Beziehungen     

Electrophysical properties of ionic alloys of GaAs obtained by implanting Zn+ (150 keV) with subsequent annealing at 500–1000°C

A study is made of the electrophysical properties (N_s, _eff) of ionic alloys of GaAs obtained by implanting 150-keV Zn ions at 20 and 300°C. The ion dose D=5·10¹³–10¹⁶ ions/cm²; the alloys were subsequently annealed for 10 min in an H₂ atmosphere with temperatures in the range 500–1000°C. The optimal parameters of the ionic alloys are obtained for T_i=300°C and T_a=700°C. Thermal acceptance of the GaAs under a SiO₂ film (d0.2–0.3 m) is observed for T_a>700°C. The limiting concentration of thermal acceptors N_s(TA)3·10¹³ cm^–2) for T=1000°C and t=10 min.Translated from Izvestiya Vysshikh Uchebnykh Zavedenii, Fizika, No. 3, pp. 22–26, March, 1979.     

The Pioneer Anomaly as Acceleration of the Clocks

This work proposes an explanation of the Pioneer anomaly, the unmodelled and as yet unexplained blueshift detected in the microwave signal of the Pioneer 10 and other spaceships by Anderson et al. in 1998. What they observed is similar to the effect that would have either (i) an anomalous acceleration a_P the ship towards the Sun, or (ii) an acceleration of the clocks a_t=a_P/c. The second alternative is investigated here, with a phenomenological model in which the anomaly is an effect of the background gravitational potential (t) that pervades all the universe and is increasing because of the expansion. It is shown that 2a_t=d /dt=d²_clocks/dt², evaluated at present time t₀, where t and _clocks are the coordinate time and the time measured by the atomic clocks, respectively. The result of a simple estimate gives the value a_t 1.8× 10^–18 s^–1, while Anderson et al. suggested a_t=(2.9±0.4) × 10^–18 s^–1 on the basis of their observations. The calculation are performed near the Newtonian limit but in the frame of general relativity.     

Search for superconducting effect on the decay of99m Tc

An experimental investigation of the influence of superconductivity on the decay rate of^99m Tc, _T, has been performed by means of a differential method. The^99m Tc samples containing⁹⁹Tc as a carrier were prepared by electrodeposition on a copper plated tungsten wire. For production of metallic technetium the samples were reduced in pure hydrogen gas at 800~1000°C. X-ray analysis of the samples showed they were surely metallic with anhcp structure. The lattice constants observed area=2.741 Å andc=4.398 Å. The transition temperature was found to be 7.5±0.2K. Comparison of two sources, normal (room temperature) and superconducting (4.2 K), did not show an appreciable effect of superconductivity on the decay rate of^99m Tc exceeding the limit of uncertainty of our experiment:/ _T=(1.1±2.7) × 10^–4.