Total and transport elastic cross-sections for excited muonic and pionic hydrogen atoms

The results of an experiment on muon catalyzed dd-fussion in HD gas are presented. The experiment was performed at the muon beam of PSI using a high-pressure ionization chamber filled with pure HD-gas of low D₂ concentration on the level 1%, at temperatures 50, 150 and 300 K. The non-resonant character of ddμ-molecule formation on HD molecules was confirmed by measuring the ratio of yields of the two ddμ-fusion channels, R=Y(³He,n)/Y(³H,p), which proved to be close to unity. The ddμ formation rate was found to vary from λ_ddμ-HD=0.05· 10⁶ s^-1 at T=50 K to λ_ddμ-HD=0.12· 10⁶ s^-1 at T=300 K, in agreement with the theoretical prediction. A prominent peak at t<60 ns was observed in the time spectrum of fusion neutrons indicating a resonant contribution of ddμ formation from epithermal dμ atoms. This revised version was published online in August 2006 with corrections to the Cover Date.     

Photoluminescence studies of Si nanocrystals

Summary We report room temperature time-resolved photoluminescence (PL) and temperature dependence of continuous wave (cw) PL studies of high fluence (from 3·10¹⁶ to 3·10¹⁷ cm⁻²) Si⁺-implanted thermal SiO₂ layers after annealing at high temperature (T=1000°C). Such measurements were related to TEM analysis of samples. Nancocrystals were observed at TEM only a samples implanted at higher fluence. In these samples a near infrared PL signal peaked at approximately 1.5 eV with decay time of about 100 μs is present. Besides, in all samples a light emission is present in the green region of the spectrum. The intensity of the emission shows large variations with ion fluence, and is characterized by 0.4, 2 and 7 ns decay times. Paper presented at the III INSEL (Incontro Nazionale sul Silicio Emettitore di Luce) Torino, 12–13 October 1995.     

In vivo NMR T2 relaxation of experimental brain tumors in the cat: A multiparameter tissue characterization

Experimental gliomas (F98) were inoculated in cat brain for the systematic study of their in vivo T₂ relaxation time behavior. With a CPMG multi-echo imaging sequence, a train of 16 echoes was evaluated to obtain the transverse relaxation time and the magnetization M(0) at time t = 0. The magnetization decay curves were analyzed for biexponentiality. All tissues showed monoexponential T₂, only that of the ventricular fluid and part of the vital tumor tissue were biexponential. Based on these NMR relaxation parameters the tissues were characterized, their correct assignment being assured by comparison with histological slices. T₂ of normal grey and white matter was 74 ± 6 and 72 ± 6 msec, respectively. These two tissue types were distinguished through M(0) which for white matter was only 0.88 of the intensity of grey matter in full agreement with water content, determined from tissue specimens. At the time of maximal tumor growth and edema spread a tissue differentiation was possible in NMR relaxation parameter images. Separation of the three tissue groups of normal tissue, tumor and edema was based on T₂ with T_2(normal) < T_2(tumor) < T_2(edema). Using M(0) as a second parameter the differentiation was supported, in particular between white matter and tumor or edema. Animals were studied at 1–4 wk after tumor implantation to study tumor development. The magnetization M(0) of both tumor and peritumoral edema went through a maximum between the second and third week of tumor growth. T₂ of edema was maximal at the same time with 133 ± 4 msec, while the relaxation time of tumor continued to increase during the whole growth period, reaching values of 114 ± 12 msec at the fourth week. Thus, a complete characterization of pathological tissues with NMR relaxometry must include a detailed study of the developmental changes of these tissues to assure correct experimental conditions for the goal of optimal contrast between normal and pathological regions in the NMR images.     

Temperature dependence of surface impedance of Tl2Ba2CaCu2O8−δ and YBa2Cu3O6.95 single crystals measured in the microwave band

The real part R _s and the imaginary part X _s of the surface impedance Z _s=R _s+ iX _s of Tl₂Ba₂CaCu₂O_8−δ and YBa₂Cu₃O_6.95 single crystals have been measured with high precision at frequency ω/2π=9.4 GHz in the temperature range 0<T<140 K. In the Tl₂Ba₂CaCu₂O_8−δ crystal a linear temperature dependence R _s(T) has been found for T⩽50 K, and the magnetic field penetration depth λ(4.2 K)=X _s(4.2 K)/ω μ ₀≈3760 Å has been measured. Along with well known features of the function Z _s(T) in high-quality YBa₂Cu₃O_6.95 single crystals, such as the linearity of λ(T) and R _s(T) for T<T _c/3 and a maximum of R _s(T) at T∼T _c/2, the linearity range of λ(T) extends to T≃50 K, and this curve has a plateau in the range 60<T<85 K. The curve of R _s(T) in both the superconducting and normal states of YBa₂Cu₃O_6.95 is well described by a two-fluid model with the electron-phonon mechanism of quasiparticle relaxation. A formula describing the curve of λ ²(0)/λ ²(T) throughout the studied temperature range is also given. Zh. éksp. Teor. Fiz. 112, 2210–2222 (December 1997)     

Muon/Muonium in an Isotopically Pure 13C Diamond

A preliminary study of the diamagnetic (μ_d) and the paramagnetic (Mu _T ) states in a synthetic ¹³C diamond has been performed using the Transverse Field Muon Spin Rotation method. This system could be used to verify the quantum diffusion behaviour observed before, however, with a more reliable extraction of the hopping rate. The results were obtained in an applied magnetic field of 7.5 mT and at sample temperatures of 10 K, 100 K and 200 K. The prompt fraction, f, of the μ_d state remains constant at 22(5)% in the range 10–200 K; that of the Mu _T state increases from 53(10)% at 10 K to 78(10)% at 200 K. The fractions of the two states add to 100% at 200 K, suggesting non-population of the bond-centred state, Mu_BC, which is often observed in other diamond samples. The μ_d state has a spin relaxation rate of 0.20(5) μs⁻¹, in contrast to the zero value obtained in type II diamond samples. This indicates appreciable interaction of the μ_d state with the ¹³C atoms. The Mu _T state has a large spin relaxation rate ranging from 3.0(5) μs⁻¹ at 10 K to 7.0(5) μs⁻¹ at 200 K, consistent with values obtained in diamond samples with defects. This work is part of ongoing studies of muon/muonium-defect interactions in diamonds. This revised version was published online in September 2006 with corrections to the Cover Date.     

Effects of time delay on the statistical fluctuations for a bistable system driven by cross-correlated noises

We study the effects of time delay on the normalized correlation function C(s) and the associated relaxation time T _c for a bistable system with correlations between multiplicative and additive white noises under the condition of small time delay. Using the projection operator method, the expressions of T _c and C(s) are obtained. Based on numerical computations, it is found that the delay time τ slows down the rate of fluctuation decay of dynamical variable for the presence of positive feedback intensity (∈ > 0), while speeds up the rate of fluctuation decay of dynamical variable for the presence of negative feedback intensity (∈ < 0). The effects of the delay time τ on the T _c and C(s) are entirely opposite for ∈ 〉 0 and ∈ < 0.      

Interaction of Muons with H2/H3-Centres in Diamond

We report on transverse field muon spin rotation measurements on a nitrogen-rich type Ia diamond, both before and after the conversion of some of the aggregated nitrogen centres to nitrogen-vacancy complexes known as H2/H3-centres. The prompt fractions f and the spin relaxation rates λ were determined for the diamagnetic (μ_d) and the paramagnetic (Mu_T) states in the temperature range 10–300 K. The production of the nitrogen-vacancy complexes had little effect on the parameters of the Mu_T state for which f and λ remained unchanged at approximately 30% and 4 μs⁻¹, respectively. For the μ_d state, on the other hand, the formation of the H2/H3-centres resulted in an increase of the prompt fraction from 10(2)% to 20(3)%, and (for the first time) the spin relaxation rate showed a non-zero value of 0.020(3) μs⁻¹. These results show evidence of strong μ_d interactions with the nitrogen-vacancy complexes in diamond, and suggest a more complex structure for this state than a bare μ⁺. This revised version was published online in September 2006 with corrections to the Cover Date.     

Lifetime measurements of Rydberg states in the 6snd 1 D 2-series of BaI

We have measured the lifetimes of 10 Rydberg states from 6s8d ¹ D ₂ to 6s 17d ¹D₂ in the Ba I spectrum by time-resolved recording of the exponential decay of the resonance fluorescence in an atomic beam. The excitation was performed by use of two pulsed dye lasers simultaneously pumped by one nitrogen laser. The lifetime results differ strongly from Coulomb approximation calculations and show deviations from a(n ^*)³-dependence.     

BCS-BEC crossover and quantum hydrodynamics in <Emphasis Type="Italic">p</Emphasis>-wave superfluids with a symmetry of the <Emphasis Type="Italic">A</Emphasis>1 phase

We solve the Leggett equations for the BCS-BEC crossover in a three dimensional resonance p-wave superfluid with the symmetry of the A1 phase. We calculate the sound velocity, the normal density, and the specific heat for the BCS domain (μ > 0), for the BEC domain (μ < 0), and close to the important point μ = 0 in the 100% polarized case. We find the indications of a quantum phase transition close to the point μ(T = 0) = 0. Deep in the BCS and BEC domains, the crossover ideas of Leggett, Nozieres, and Schmitt-Rink work quite well. We discuss the spectrum of orbital waves, the paradox of intrinsic angular momentum and the complicated problem of chiral anomaly in the BCS A1 phase at T = 0. We present two different approaches to the chiral anomaly, based on supersymmetric hydrodynamics and on the formal analogy with the Dirac equation in quantum electrodynamics. We evaluate the damping of nodal fermions due to different decay processes in the superclean case at T = 0 and find that a ballistic regime ωτ ≫ 1 occurs. We propose to use aerogel or nonmagnetic impurities to reach the hydrodynamic regime ωτ ≪ 1 at T = 0. We discuss the concept of the spectral flow and exact cancelations between time derivatives of anomalous and quasiparticle currents in the equation for the total linear momentum conservation. We propose to derive and solve the kinetic equation for the nodal quasiparticles in both the hydrodynamic and ballistic regimes to demonstrate this cancelation explicitly. We briefly discuss the role of the other residual interactions different from damping and invite experimentalists to measure the spectrum and damping of orbital waves in the A phase of ³He at low temperatures.     

Reductive Fluorescence Quenching of the Photoexcited Free Base <Emphasis Type="Italic">meso</Emphasis>-Tetrakis (Pentafluorophenyl) Porphyrin by Amines

Steady state and time resolved fluorescence quenching behaviors of meso-Tetrakis (pentafluorophenyl) porphyrin (H₂F₂₀TPP) in presence of different aliphatic and aromatic amines have been executed in homogeneous dichloromethane (DCM) solution. At room temperature in DCM, free base (H₂F₂₀TPP) shows fluorescence with two distinct peaks at 640 and 711 nm and natural lifetime τ _f = 9.8 ns which are very similar to that of meso-tetraphenyl porphyrin (TPP). Unlike TPP, addition of both aliphatic and aromatic amines to a solution containing H₂F₂₀TPP results in an efficient decrease in fluorescence intensity without altering the shape and peak position of fluorescence emission. Upon addition of amines there was no change in optical absorption spectra of H₂F₂₀TPP. The fluorescence quenching rate constants ranged from 1 × 10⁹ to 4 × 10⁹ s⁻¹, which are one order below to the diffusion control limit, and temperature dependent quenching rate constants yield the activation energies which are found to be order of 0.1 eV. Femto second transient absorption studies reveal the existence of amine cation radical and porphyrin anion radicals with very short decay time (15 ps). The fluorescence quenching reaction follows Stern–Volmer kinetics. Steady state and time-resolved data are interpreted within general kinetic scheme of Marcus semi-classical model which attributes bimolecular electron transfer process between amines and the lowest excited singlet state of H₂F₂₀TPP. Calculated internal reorganization energies are found to be in between 0.04 and 0.22 ev. Variation of electron transfer rate as function of free energy change (∆G⁰) points the ET reactions in the present systems are in Marcus normal region. This is the first example of reductive fluorescence quenching of free base neutral porphyrins in homogeneous organic solvent ever known.     

Muon catalyzed fusion and muon to 3He transfer in solid T2 studied by X-ray and neutron detection

X-ray and neutron measurements were carried out for muon catalyzed fusion and related phenomena in solid T₂. The X-ray originated from the μ^- to α sticking in muon catalyzed fusion; t + t + μ ^- → (μ ^- α) + 2n was measured for the first time, yielding K _α X-ray intensity of (μα) atom and the intensity ratio of K _β to K _α . Utilizing the phenomena of ³He accumulation in solid T₂, the X-ray in the μ^- transfer process from (tμ) to ³He was detected, providing a formation rate and radiative decay branching-ratio of (t ³Heμ) molecule. From fusion neutron measurements, estimated values were obtained for (ttμ) molecular formation rate as well as sticking probability ω_t in ttμ fusion. A possible new insight in t + t fusion reaction process at a low energy limit is also obtained. This revised version was published online in August 2006 with corrections to the Cover Date.     

Spontaneous-emission spectrum in a cavity: Doublet or triplet?

Summary The Green’s functions formalism together with the new algorithm in operating with ζ-functions has been used to obtain the three-peaked spectrum of spontaneous emission of an atom in a weakly damped cavity. The single-peaked spectrum and exponential decay law with the short (τ_s ~ 1/Γ _c) and long (τ₁ ~Γ _c/g ²) decay times have been shown to exist in the strongly damped cavity with its passive linewidthΓ _c.     

First measurement of the ϱ spectral function in nuclear collisions

The NA60 experiment at the CERN SPS has studied low-mass muon pairs in 158 A GeV In–In collisions. A strong excess of pairs is observed above the yield expected from neutral meson decays. The unprecedented sample size close to 400000 events and the good mass resolution of about 2% made it possible to isolate the excess by subtraction of the decay sources. The shape of the resulting mass spectrum shows some non-trivial centrality dependence, but is largely consistent with a dominant contribution from π⁺π^-→ϱ→μ⁺μ^- annihilation. The associated ϱ spectral function exhibits considerable broadening, but essentially no shift in mass. The p_T-differential mass spectra show the excess to be much stronger at low p_T than at high p_T. The results are compared to theoretical model predictions; they tend to rule out models linking hadron masses directly to the chiral condensate. PACS 25.75.-q; 12.38.Mh; 13.85.Qk     

Stress-Induced Alteration of Chlorophyll Fluorescence Polarization and Spectrum in Leaves of <Emphasis Type="Italic">Alocasia macrorrhiza</Emphasis> L. Schott

The value of intrinsic chlorophyll fluorescence polarization, and the intensity in emission spectrum were investigated in leaf segments of Alocasia macrorrhiza under several stress conditions including different temperatures (25–50°C), various concentrations of NaCl (0–250 mM), methyl viologen (MV, 0–25 μM), SDS (0–1.0%) and NaHSO₃ (0–80 μM). Fluorescence emission spectrum of leaves at wavelength regions of 500–800 nm was monitored by excitation at 436 nm. The value of fluorescence polarization (P value), as result of energy transfer and mutual orientation between chlorophyll molecules, was determined by excitation at 436 nm and emission at 685 nm. The results showed that elevated temperature and concentrations of salt (NaCl), photooxidant (MV), surfactant (SDS) and simulated SO₂ (NaHSO₃) treatments all induced a reduction of fluorescence polarization to various degrees. However, alteration of the fluorescence spectrum and emission intensity of F₆₈₅ and F₇₃₁ depended on the individual treatment. Increase in temperature and concentration of NaHSO₃ enhanced fluorescence intensity mainly at F₆₈₅, while an increase in MV concentration led to a decrease at both F₆₈₅ and F₇₃₁. On the contrary, NaCl and SDS did not cause remarkable change in fluorescence spectrum. Among different treatments, the negative correlation between polarization and fluorescence intensity was found with NaHSO₃ treatments only. We concluded that P value being measured with intrinsic chlorophyll fluorescence as probe in leaves is a susceptible indicator responding to changes in environmental conditions. The alteration of P value and fluorescence intensity might not always be shown a functional relation pattern. The possible reasons of differed response to various treatments were discussed.     

Color and luminescence centers in LiF(U) crystals irradiated by pulsed electron beams

Characteristics of color and luminescent centers produced in LiF:U⁶⁺ (0.01M%) crystals by pulses of accelerated electrons (0.25 MeV, 15 ns, 8–200 mJ/cm²) at 77–350 K are studied using time-resolved optical spectroscopy. It is found that the time constant of the exponential rise of the cathodoluminescence intensity in the visual spectral range after completion of the irradiation pulse coincides with the decay time of a group of lines in the UV region at T = 77–280 K and with the decay time of the number of V _k -centers induced by the pulse of irradiation at T > 280 K. The mechanisms of population of the ground radiative level of the emission center and the structure of its electronic and nuclear subsystems are discussed.     

Lifetime of metastable fluorine atoms

For laser collimation of neutral F atoms, a resonance transition cycle between the metastable and the upper excited states (3s⁴ P _5/2?3p⁴ D ⁰ _7/2) can be used as a two-level closed system. We have determined the lifetime of the metastable state (3s⁴ P _5/2) in F atoms by measuring the decay curve of the fluorescence intensity as a function of distance from the plasma source. Combining the measured velocity of F radicals from the Doppler shift of the fluorescence peak, we have obtained the lifetime of the F metastable state as 3.7±0.5 μs. With this short metastable lifetime of F radicals, the simple Doppler cooling method using spontaneous light force is not practical for laser collimation of F radicals. Use of stimulated light force may be necessary to collimate F radical beams in a short distance. Received: 4 July 2000 / Published online: 13 September 2000     

μ + SR studies of antiferromagnetic chromiumSR studies of antiferromagnetic chromium

μ ⁺ SR measurements have been performed on Cr single crystals at temperatures 60 mK≤T≤295 K in applied magnetic fields 0≤B _appl≤1.5 T. The temperature dependence of the observed precession frequencies and transverse relaxation rates can be explained by the assumption that theμ ⁺ are hopping between adjacent tetrahedral interstices. At temperaturesT≤11 K evidence for an interaction between theμ ⁺ and the spin-density waves in Cr has been found. The directions and magnitudes of the lattice magnetic moments are unaffected by the applied magnetic fields.     

Optical and spectroscopic characterization of Nd-doped aluminosilicate fiber preforms made by the MCVD method using chelate delivery

4 F_3/2 level of Nd³⁺ in aluminosilicate optical fiber preforms after 807-nm excitation are reported in the temperature range from 15 °C to 500 °C for Nd₂O₃ concentrations in the range from 0.2 to [%wt]0.9 and Al₂O₃ concentrations of between [%wt]3.8 and [%wt]8. At room temperature it is observed that for concentrations of less than [%wt]0.6 Nd₂O₃ the fluorescence decay is approximately exponential; for the higher Nd₂O₃ concentrations the decay is increasingly bi-exponential. We have identified a “slow” (≈500 μs) and a “fast” (≈100 μs) decay time; the slow decay is attributed to isolated ions and the faster decay to energy transfer between homogeneously dispersed ions. The measured 1/e folding fluorescence decay time τ decreases slowly at a constant rate of -0.08±0.007 μs/K for [%wt]0.9 Nd₂O₃. It is shown that increasing the Al₂O₃ concentration tends to suppress this temperature quenching effect. A radiative decay time of 640 μs is obtained by Judd–Ofelt analysis. Received: 24 October 1997/Revised version: 2 February 1998     

The Influence of Human Serum Albumin on The Photogeneration of Singlet Oxygen by meso-Tetra(4-Sulfonatophenyl)Porphyrin. An Infrared Phosphorescence Study

meso-Tetra(4-sulfonatophenyl)porphyrin (TPPS₄) is a water soluble photosensitizer, which is currently clinically tested as a PDT drug. In our contribution, we present IR spectral- and time-resolved phosphorescence data reflecting the influence of human serum albumin (HSA) on singlet oxygen photogeneration by TPPS₄. IR emission of TPPS₄ was studied in samples containing various concentrations of HSA in phosphate buffer. The observed changes in spectral and temporal behaviour of TPPS₄ and singlet oxygen phosphorescence caused by the addition of HSA are equivalent to the effect of nitrogen purging of HSA-free solutions of TPPS₄. The main feature induced by addition of HSA appears to be the occurrence of a long-lived (tens of microseconds) photosensitizer phosphorescence at 900 nm besides ordinary short-lived (≈2 μs) one at 820 nm. It is accompanied by presence of a long-lived component of singlet oxygen emission with lifetime roughly corresponding to that of the long photosensitizer phosphorescence component. Moreover, the quantum yield of singlet oxygen phosphorescence decreases with increasing HSA concentration, while total quantum yield of TPPS₄ phosphorescence rises. These facts are explained by a shielding effect of HSA on bound molecules of TPPS₄ against quenching by oxygen which is analogous to oxygen removal by nitrogen purging.     

Characteristic features of the temperature dependence of the surface impedance of YBa2Cu3O6.95 single crystals

The real and imaginary parts of the surface impedance Z _s =R _s +iX _s of YBa₂Cu₃O_6.95 single crystals are measured at a frequency ω/π=9.4 GHz. The quantities R _s (T) and X _s (T) are linear functions of temperature for T<0.3T _c (T _c =93.5 K). A maximum of R _s (T) and a plateau of X _s (T) are observed in the interval 35<T<65 K. Our experimental data, just as all recent measurements of R _s (T) in YBa₂Cu₃O_6.95 single crystals in the temperature range 0<T<1.3T _c , are described well in a two-fluid model which assumes electron-phonon scattering of quasiparticles. Pis’ma Zh. éksp. Teor. Fiz. 65, No. 12, 893–898 (25 June 1997)