Double-beta decay of <Superscript>150</Superscript>Nd to the first 0<Superscript>+</Superscript> excited state of <Superscript>150</Superscript>Sm

Two-neutrino-double-beta decay of ¹⁵⁰Nd to the first 0⁺ excited state in ¹⁵⁰Sm is investigated with a 400-cm³ low-background HPGe detector. Data analysis for 11320.5 h shows an excess of events at 333.9 and 406.5 keV. This allows us to estimate the half-life of the investigated process as [1.4 _?0.2 ^+0.4 ±0.3(syst.)]×10²⁰ yr.     

Double-beta decay of <Superscript>150</Superscript>Nd to the first 0<Superscript>+</Superscript> excited state of <Superscript>150</Superscript> Sm: Current state

Two-neutrino double-beta decay of ¹⁵⁰Nd to the first 0⁺ excited state in ¹⁵⁰Sm is investigated with the 400-cm³ low-background HPGe detector. Preliminary data analysis for 6843 h shows an excess of events at 333.9 and 406.5 keV. If this excess is assigned to the investigated transition, then its half-life can be estimated at [1.2 _?0.3 ^+0.5 ±0.4(syst.)]×10²⁰ yr.     

Negative-muon capture in <Superscript>150</Superscript>Sm

The energy and time spectra of γ rays emitted during negative-muon capture in ¹⁵⁰Sm were studied. The total muon lifetime in ¹⁵⁰Sm was measured. The yields of several radioactive isotopes in this reaction were determined. The partial γ-ray yield upon muon capture by a ¹⁵⁰Sm nucleus were measured.     

Effect of high doses of N<Superscript>+</Superscript>, N<Superscript>+</Superscript> + Ni<Superscript>+</Superscript>, and Mo<Superscript>+</Superscript> + W<Superscript>+</Superscript> ions on the physicomechanical properties of TiNi

The surface layer of an equiatomic TiNi alloy, which exhibits the shape memory effect in the martensitic state, is modified with high-dose implantation of 65-keV N⁺ ions (the implantation dose is varied from 10¹⁷ to 10¹⁸ ions/cm²). TiNi samples are implanted by N⁺, Ni⁺-N⁺, and Mo⁺-W⁺ ions at a dose of 10¹⁷–10¹⁸ cm⁻² and studied by Rutherford backscattering, scanning electron microscopy, energy dispersive spectroscopy, X-ray diffraction (glancing geometry), and by measuring the nanohardness and the elastic modulus. A Ni⁺ concentration peak is detected between two maxima in the depth profile of the N⁺ ion concentration. X-ray diffraction (glancing geometry) of TiNi samples implanted by Ni⁺ and N⁺ ions shows the formation of the TiNi (B2), TiN, and Ni₃N phases. In the initial state, the elastic modulus of the samples is E = 56 GPa at a hardness of H = 2.13 ± 0.30 GPa (at a depth of 150 nm). After double implantation by Ni⁺-N⁺ and W⁺-Mo⁺ ions, the hardness of the TiNi samples is ∼2.78 ± 0.95 GPa at a depth of 150 nm and 4.95 ± 2.25 GPa at a depth of 50 nm; the elastic modulus is 59 GPa. Annealing of the samples at 550°C leads to an increase in the hardness to 4.44 ± 1.45 GPa and a sharp increase in the elastic modulus to 236 ± 39 GPa. A correlation between the elemental composition, microstructure, shape memory effect, and mechanical properties of the near-surface layer in TiNi is found.     

Nuclear deformation and the two-neutrino double- β decay in <Superscript>124, 126</Superscript>Xe , <Superscript>128, 130</Superscript>Te , <Superscript>130, 132</Superscript>Ba and <Superscript>150</Superscript>Nd isotopes

The two-neutrino double-beta decay of ^{124, 126}Xe , ^{128, 130}Te , ^{130, 132}Ba and ¹⁵⁰Nd isotopes is studied in the Projected Hartree-Fock-Bogoliubov (PHFB) model. Theoretical 2ν β^-β^- half-lives of ^{128, 130}Te , and ¹⁵⁰Nd isotopes, and 2ν β⁺β⁺ , 2ν β⁺ EC and 2ν ECEC for ^{124, 126}Xe and ^{130, 132}Ba nuclei are presented. Calculated quadrupolar transition probabilities B(E2 : 0⁺ → 2⁺) , static quadrupole moments and g -factors in the parent and daughter nuclei reproduce the experimental information, validating the reliability of the model wave functions. The anticorrelation between nuclear deformation and the nuclear transition matrix element M _2ν is confirmed.     

Enhanced Up-Conversion Emission in Al<Superscript>3+</Superscript> Co-Doped ZnGa<Subscript>2</Subscript>O<Subscript>4</Subscript>:Yb<Superscript>3+</Superscript>,Tm<Superscript>3+</Superscript> Powder Phosphors

Yb³⁺-Tm³⁺ co-doped up-conversion powder phosphors using Zn(Al_xGa_1-x)₂O₄ (ZAGO) as the host materials were synthesized via solid-state reaction successfully. In addition, the morphology, structural characterization and up-conversion luminescent properties were all investigated by scanning electron microscope (SEM), x-ray diffraction (XRD) and fluorescence spectrophotometer (F-7000), respectively. Under the excitation of a 980 nm laser, all as-prepared powders can carry out blue emission at about 477 nm (corresponding to ¹G₄ → ³H₆ transition of Tm³⁺ ions), and red emission at about 691 nm (attributed to ³F₃ → ³H₆ transition of Tm³⁺ ions). Also, the influence of doping Al³⁺ ions were investigated. In brief, the doping of Al³⁺ ions has no effect on the position of emission peak. Howbeit the up-conversion efficiency and intensity of ZAGO:Yb,Tm phosphors are stronger than ZGO:Yb,Tm and ZAO:Yb,Tm phosphors, while the crystallinity is the opposite. More particularly, all as-prepared powder phosphors emit strong luminescence, which is observable by the naked eye, demonstrating the potential applications in luminous paint, luminescent dye, etc.     

Description of elastic scattering in the <Superscript>16</Superscript>O + <Superscript>16</Superscript>O and <Superscript>16</Superscript>O + <Superscript>12</Superscript>C systems

The objective of the present study was to describe more precisely experimental data on elastic scattering in the ¹⁶O + ¹⁶O system at E _lab = 124, 145, 250, 350, and 480 MeV and in the ¹⁶O + ¹²C system at E _lab = 132, 170, 181, 200, 230, 260, and 281 MeV. The role of exchange interaction in the region of backward angles is investigated. The coefficient of incompressibility of nuclear matter is estimated at K = 205 MeV ± 15%.     

Near infrared lights emission of <Superscript>40</Superscript>Ar<Superscript>16+</Superscript> impacting on metal surfaces

The highly charged ion ⁴⁰Ar¹⁶⁺ with the velocity (kinetic energy E _K=150 keV, velocity V=8.5×10⁵ m/s) smaller than Bohr velocity (V _Bohr=2.9×10⁶ m/s) was found to hove impacts on the surfaces of metals Ni, Mo, Au and Al, and the Ar atomic infrared light lines and X-rays spectra were simultaneously measured. The experimental results show that the highly charged ion that captures electrons is neutralized, and the multiply-excited hollow atom forms. The hollow atom cascade decay radiates lights from infrared to X-ray spectrum. The intensity of infrared lights shows that the metallic work functions play an important role in the neutralization process of highly charged ions during their interaction with metallic surfaces, which verifies the classical over-the-barrier model. Supported by the National Natural Science Foundation of China (Grant No. 10574132), the Natural Science Foundation of Shaanxi Province (Grant No. 2007A05) and the Talents Introduction Project of Xianyang Normal University (Grant No. 05XSYK103)     

Double-beta decay of <Superscript>100</Superscript>Mo to 0<Superscript>+</Superscript> excited states in <Superscript>100</Superscript>Ru

A brief review on the 2νββ decay of ¹⁰⁰Mo to the 0⁺ excited state in ¹⁰⁰Ru is performed. A weighted-average half-life value for the decay has been obtained, T_1/2 = (6.8 ± 1.2) × 10²⁰ yr. The corresponding average value for the nuclear matrix element was extracted, 0.095 ± 0.009.     

Aspects of radiative K<Superscript>+</Superscript><Subscript>e3</Subscript> decays

We re-investigate the radiative charged kaon decay K^±→π⁰e^±ν_eγ [K_e3γ ^±] in chiral perturbation theory, merging the chiral expansion with Low’s theorem. We thoroughly analyze the precision of the predicted branching ratio relative to the non-radiative decay channel. Structure dependent terms and their impact on differential decay distributions are investigated in detail, and the possibility to see effects of the chiral anomaly in this decay channel is emphasized. PACS 13.20.Eb; 11.30.Rd; 12.39.Fe     

A miniature tunable TEA CO<Subscript>2</Subscript> laser using isotope <Superscript>13</Superscript>C<Superscript>16</Superscript>O<Subscript>2</Subscript> and <Superscript>12</Superscript>C<Superscript>16</Superscript>O<Subscript>2</Subscript>

A miniature tunable TEA CO₂ laser using isotope ¹³C¹⁶O₂ as the active medium is developed to extend the spectral range of CO₂ lasers for further application. The optimization of the energy parameters of the tunable TEA ¹³C¹⁶O₂ laser and the same laser using ¹²C¹⁶O₂ are studied. When a gas mixture (¹³C¹⁶O₂: N₂: He = 1: 1: 3) at a total pressure of 6.4 × 10⁴ Pa is used, the TEA ¹³C¹⁶O₂ laser of a 45-cm³ active volume obtains 51 emission lines in the [00⁰1–10⁰0] and [00⁰1–02⁰0] bands. The maximum pulse energy of the TEA ¹³C¹⁶O₂ laser is about 357 mJ. The same laser using the conventional gas mixture (¹²C¹⁶O₂: N₂: He = 1: 1: 3) at a pressure of 6.66 × 10⁴ Pa is measured to obtain 69 laser emission lines and the maximum pulse energy of laser radiation is about 409 mJ.     

II. Electron-impact dissociative excitation of C<Subscript>2</Subscript>H<Stack><Subscript>2</Subscript><Superscript>+</Superscript></Stack> and C<Subscript>2</Subscript>D<Stack><Subscript>2</Subscript><Superscript>+</Superscript></Stack>

Absolute cross-sections for electron-impact dissociative ionization of C₂ H₂⁺ and C₂ D₂⁺ to CH⁺, C⁺, C₂⁺ , H⁺, CH₂⁺ and C₂D⁺ fragments are determined for electron energies ranging from the corresponding threshold to 2.5 keV. Results obtained in a crossed beams experiment are analyzed to estimate the contribution of dissociative ionization to each fragment formation. The dissociative ionization cross sections are seen to decrease for more than an order of magnitude, from CH⁺ (5.37±0.10) × 10^-17 cm² over C⁺ (4.19± 0.16) × 10^-17 cm², C₂D⁺ (3.94±0.38) × 10^-17 cm², C₂⁺ (3.82±0.15) × 10^-17 cm² and H⁺ (3.37±0.21) × 10^-17 cm² to CH₂⁺ (2.66±0.14) × 10^-18 cm². Kinetic energy release distributions of fragment ions are also determined from the analysis of the product velocity distribution. Cross section values, threshold energies and kinetic energies are compared with the data available from the literature. Conforming to the scheme used in the study of the dissociative excitation of C₂H₂⁺ ( C₂ D₂⁺ )\left( {\rm C}_2 {\rm D}_2^+ \right), the cross-sections are presented in a format suitable for their implementation in plasma simulation codes.     

Improvement of thermal and spectroscopic behavior of Er<Superscript>3+</Superscript>/Ce<Superscript>3+</Superscript> co-doped tellurite glass for lasing materials

Tellurite glasses (TeO₂–ZnO–Nb₂O₅) mono-doped Er³⁺ and co-doped Er³⁺/Ce³⁺ have been prepared using the melt-quenching technique. To evaluate the effect of Ce³⁺ on the structural, thermal stability of glass hosts and fluorescence properties of Er³⁺, X-ray diffraction patterns, Ftir spectra, differential scanning calorimeter curves, absorption spectra, fluorescence emission spectra, fluorescence lifetimes, up-conversion emission spectra of glass samples were measured and investigated. Using Judd–Ofelt theory, we calculated intensity parameters (Ω₂, Ω₄ and Ω₆), spontaneous emission probabilities, the radiative lifetime, luminescence branching factors and the quantum yield of luminescence for ⁴I_13/2 → ⁴I_15/2 transition. The co-doping with Ce³⁺ was effective on the suppression of up-conversion emission of Er³⁺ owing to the phonon-assisted energy transfer: Er³⁺:⁴I_11/2 + Ce³⁺:²F_5/2 → Er³⁺:⁴I_13/2 + Ce³⁺:²F_7/2 which contributed the effective enhancement of 1.53 µm fluorescence emission. The change in optical properties with the addition of Ce³⁺ ions have been discussed and compared with other glasses. Using the Mc Cumber method for the ⁴I_13/2 → ⁴I_15/2 transition, absorption cross-section, calculated emission cross-section, and gain cross-section values support that TZNEr1Ce1 glass is a potential material for developing broad-band and high-gain erbium-doped fiber amplifiers applied for 1.53 µm.     

I. Electron-impact ionization and dissociation of C<Subscript>2</Subscript>H<Stack><Subscript>2</Subscript><Superscript>+</Superscript></Stack> and C<Subscript>2</Subscript>D<Stack><Subscript>2</Subscript><Superscript>+</Superscript></Stack>

Absolute cross-sections for electron-impact ionization and dissociation of C₂H₂⁺ and C₂D₂⁺ have been measured for electron energies ranging from the corresponding thresholds up to 2.5 keV. The animated crossed beams experiment has been used. Light as well as heavy fragment ions that are produced from the ionization and the dissociation of the target have been detected for the first time. The maximum of the cross-section for single ionization is found to be (5.56 ± 0.03)× 10^-17 cm² around 140 eV. Cross-sections for dissociation of C₂ H₂⁺ (C₂D₂⁺) to ionic products are seen to decrease for two orders of magnitude, from C₂D⁺ (12.6 ± 0.3) × 10^-17 cm² over CH⁺(9.55 ± 0.06) × 10^-17 cm², C⁺ (6.66 ± 0.05) × 10^-17 cm², C₂⁺ (5.36 ± 0.27) × 10^-17 cm², H⁺ (4.73 ± 0.29) × 10^-17 cm² and CH₂⁺ (4.56 ± 0.27) × 10^-18 cm² to H₂⁺ (5.68 ± 0.49) × 10^-19 cm². Absolute cross-sections and threshold energies have been compared with the scarce data available in the literature.     

Super-allowed α decay above doubly-magic <Superscript>100</Superscript>Sn and properties of <Superscript>104</Superscript>Te = <Superscript>100</Superscript>Sn ⊗ α

α-decay half-lives for ^{104, 105, 106}Te and ^{108, 109, 110}Xe close above the doubly-magic ¹⁰⁰Sn are calculated from systematic double-folding potentials. The derived α preformation factors are compared to results for ^{212, 213, 214}Po and ^{216, 217, 218}Rn above the doubly-magic ²⁰⁸Pb. α-decay energies of Q _α = 5.42±0.07MeV and 4.65±0.15MeV are predicted for ¹⁰⁴Te and ¹⁰⁸Xe; the corresponding half-lives are T _1/2 ≈ 5ns for ¹⁰⁴Te and of the order of 60μs for ¹⁰⁸Xe. Additionally, the properties of rotational bands in ¹⁰⁴Te are analyzed, and the first excited 2⁺ state in ¹⁰⁴Te is predicted at E _x = 650±40keV; it decays preferentially by γ emission with a reduced transition strength of 10 Weisskopf units to the ground state of ¹⁰⁴Te and with a minor branch by α emission to the ground state of ¹⁰⁰Sn.     

Nanoparticles size effects in thermoluminescence of oxyfluoride glass-ceramics containing Sm<Superscript>3+</Superscript>-doped CaF<Subscript>2</Subscript> nanocrystals

Oxyfluoride glass-ceramic in the system SiO₂–Al₂O₃–CaF₂–SmF₃ containing Sm³⁺-doped CaF₂ nanocrystals in the range from 15 to 150 nm size were produced by using the controlled ceramization of the precursor glass. The incorporation of the Sm³⁺-dopant ion in the glass ceramic creates new electron-trapping centers and thermoluminescence (TL) method has been used in order to trace their evolution during glass ceramization. The 370 °C TL peak observed in precursor glass has been assigned to the recombination of the electrons released from the Sm²⁺-traps in the amorphous glass network. In the glass-ceramic sample containing nanocrystals with about 15 nm size the new weak TL peaks at 270, 290, and 310 °C were attributed to the recombination of the electrons released from the Sm²⁺-traps located mainly at the surface of the CaF₂ nanocrystals. In the glass-ceramic sample containing nanocrystals with about 150 nm size, the new TL peaks at 232, 270, and 302 °C size have been assigned to the recombination of the electrons released from the Sm²⁺-traps located inside the CaF₂ nanocrystals.     

Green,blue, red,near-infrared up-conversion luminescence of Yb<Superscript>3+</Superscript>/Er<Superscript>3+</Superscript>/Tm<Superscript>3+</Superscript> co-doped YVO<Subscript>4</Subscript> nanoparticles

YVO₄:Yb³⁺,Er³⁺; YVO₄:Yb³⁺,Tm³⁺; and YVO₄:Yb³⁺,Er³⁺,Tm³⁺ were all synthesized via sol-gel method with a subsequent thermal treatment. Specifically, YVO₄:Yb³⁺,Er³⁺,Tm³⁺ phosphors were prepared with different annealing temperatures to study the influence of temperature. The transmission electron microscope (TEM), scanning electron microscope (SEM), X-ray diffractometer (XRD), and photoluminescent (PL) spectrofluorometer were used to investigate the morphology, crystal structure, and up-conversion luminescent properties of all samples. In summary, all samples were granular-like nanoparticles and well crystallized with the same tetragonal phase as YVO₄. Under the irradiation at 980 nm, YVO₄:Yb³⁺,Er³⁺ phosphors can generate green emission at 525 and 553 nm and red emission at 657 nm, while YVO₄:Yb³⁺,Tm³⁺ phosphors can generate blue emission at 476 nm, red emission at 648 nm, and near-infrared emission at 800 nm. Notably, YVO₄:Yb³⁺,Er³⁺,Tm³⁺ samples can exhibit green emission, blue emission, red emission, and near-infrared emission at the same time, which might endow the as-prepared samples with potential applications in many fields, such as luminous paint, infrared detection, and biological label.     

Neutron single-particle structure of <Superscript>48</Superscript>Ca, <Superscript>50</Superscript>Ti, <Superscript>52</Superscript>Cr, <Superscript>54</Superscript>Fe,and <Superscript>56</Superscript>Ni nuclei

The change in the neutron single-particle structure of (1f?2p)-shell magic nuclei near the Fermi energy with an increase in the number of protons in the 1f _7/2 subshell from 0 for ⁴⁸Ca to 8 for ⁵⁶Ni has been investigated. Good agreement of the experimental and estimated values of the single-particle energies E _nlj of the bound states of neutrons in these nuclei with the results of calculations within the dispersive optical model is obtained.     

Search for the double-beta decay of <Superscript>130</Superscript>Te to excited states in <Superscript>130</Superscript>Xe

Experimental limits on the half-lives with respect to the (0ν+2ν) double-beta decay of ¹³⁰Te to excited states in ¹³⁰Xe are obtained by using low-background HPGe detectors. At a 90% C.L., they are 1.6×10²¹, 2.7×10²¹, and 2.3×10²¹ yr for transitions to the 2 ₁ ⁺ , 2 ₂ ⁺ , and 0 ₁ ⁺ levels, respectively.     

Investigation of the Mn-doped compound CuGaTe<Subscript>2</Subscript> by <Superscript>63</Superscript>Cu AND <Superscript>69</Superscript>Ga nuclear magnetic resonance techniques

The synthesized base compound CuGaTe₂ and the Mn-doped compounds Cu_0.97Ga_0.97Mn_0.06Te₂ and Cu_0.93Ga_0.93Mn_0.14Te₂ have been investigated by using ⁶³Cu and ⁶⁹Ga NMR spectroscopy. The NMR spectra obtained testify to substantial structural distortions near the cationic positions in the crystal lattice of Mndoped samples. The constants of quadrupole coupling between ⁶³Cu and ⁶⁹Ga nuclei in the compounds investigated have been estimated.