Fast polarimetry system for the application to spin quantum non-demolition measurement

We report the development of a fast pulse polarimeter for the application to quantum non-demolition measurement of atomic spin (spin QND). The developed system was tunable to the atomic resonance of a ytterbium atom and has narrow laser line width suitable for spin QND. Using the developed polarimeter, we successfully demonstrated the measurement of the vacuum noise, with 10⁶ to 10⁷ photon number per pulse. PACS 42.25.Ja; 42.50.Lc; 42.55.Px     

Positron annihilation in synthetic zeolites

Both lifetime and angular correlation of positron annihilation have been measured for a series of synthetic zeolites for which the void structures are known fairly well. All of the zeolites had long lifetime components and a narrow momentum component which are ascribable to o-Ps and p-Ps annihilations in the voids, respectively. The correlation between the width of the p-Ps narrow component and the size of the largest voids showed a remarkable agreement with a theoretical estimate based on the spherical potential well model. The measurement of p-Ps momentum thus appears to be prospective as a tool to determine the size of voids of materials. The lifetime of the long lifetime component, on the other hand, showed a poor correlation with the void size even from a qualitative viewpoint, suggesting that factors other than the simple void size effect are dominant in determining the o-Ps lifetimes. Discussion is made on the cause of the different dependences of o-Ps and p-Ps annihilation parameters on the void size. It has also been found that p-Ps fraction is always larger than one third of the o-Ps fraction in all the zeolites studied. A discussion is presented on this point, too.Formerly, RIISOM     

Magnetic properties and domain structures of FeSiB thin films

Smooth Fe₇₈Si₁₀B₁₂ thin films were prepared by r.f. sputtering with the very slow deposition rate of 0.59 nm/min. The as-deposited films were not fully amorphous, instead α-Fe(Si) nanocrystallites were found to be embedded in the amorphous matrix. The saturation magnetostriction λ_s of the as-deposited film is about 6.5 × 10⁻⁶. After annealing at 540 °C for 1 h in an ultrahigh vacuum (4.5 × 10⁻⁵ Pa), the fraction of α-Fe(Si) crystalline phase largely increased, and correspondingly the λ_s decreased to 4.5 × 10⁻⁷. Ripple domain structures were observed in the as-deposited film, while dense stripe domains were observed in the annealed sample, characterized by a very narrow domain width of 80 nm. (1 1 0) texture and island-like configuration of α-Fe(Si) nanocrystallites formed by the annealing treatment are responsible for the perpendicular anisotropy. For the as-deposited film, the magnetization curves increased linearly with the increase of the magnetic field, and showed the very small hysteresis. On the other hand, the annealed sample clearly showed a very steep jump near the origin, which is due to the switch process of the dense stripe domain.     

Appearance of magnetic long range order in the spin ladder compound LaCuO2.5

We report here the two current topics in the ladder compounds. 1. The new ladder compound LaCuO_2.5 recently discovered by Hiroi and Takano shows a clear sign of magnetic long range order at around 125 K observed by μ⁺SR technique. This result demonstrates that the ground state of LaCuO_2.5 is not a spin liquid state, but a magnetically ordered state. 2. Superconductivity has been found in the ladder material (Sr,Ca)₁₄Cu₂₄O₄₁ under high pressure between 3 GPa and 4.5 GPa. The superconducting transition temperatures T_c (onset) are 12 K and 9 K at 3 GPa and 4.5 GPa, respectively. This revised version was published online in July 2006 with corrections to the Cover Date.     

Synthesis of diblock copolymers with cellulose derivatives. 3. Cellulose derivatives carrying a single pyrene group at the reducing-end and fluorescent studies of their self-assembly systems in aqueous NaOH solutions

Novel cellobiose and cellulose (DP _n =ca. 30) derivatives, N-(1-pyrenebutyloyl)-4-O-(β-d-glucopyranosyl)-β-d-glucopyranosylamine (6), N-(15-(1-pyrenebutyloylamino)-pentadecanoyl)-4-O-(β-d-glucopyranosyl)-β-d-glucopyranosylamine (7), N-(1-pyrenebutyloyl)-β-cellulosylamine (13), N-(15-(1-pyrenebutyloylamino)-pentadecanoyl)-β-cellulosylamine (14) carrying a pyrene group as a single fluorescent probe at the reducing end, were prepared in order to investigate their self-assembly systems in solutions. The relative intensity of the excimer emission at ca. 480 nm due to dimerized pyrenes (intensity I _E) to the monomer emission at ca. 380 nm due to isolated pyrene (intensity I _M), i.e., I _E/I _M, was monitored in various solutions. In water/dimethyl sulfoxide (DMSO) mixed solvent (0–98%, v/v), the ratio I _E/I _M remained low (0.04) for compound 6 over the range of water concentrations, indicating that pyrenes at C-1 position of compound 6 were diffused. On the other hand, the ratio I _E/I _M increased (0.04–4.96) for compound 7 with the increase in water concentration, indicating that pyrenes at C-1 position were associated. In aqueous NaOH solutions (4.4–17.5%, w/w), compound 14 showed a large increase in the ratio I _E/I _M (0.84–8.14) with the increase in NaOH concentration, compared to compound 13 (0.06–0.41). It was found that the association of hydrophobic groups at the reducing-end of cellulose could be controlled by the hydrophilic–hydrophobic balance of compounds and the solvent polarity.