Index-of-refraction sensors: virtually unlimited sensing power at the critical angle

In an effort to improve and simplify refractive index sensors, we identified a basic operation mode at the critical angle. Sensitivity to the refractive index is higher than in standard surface plasmon resonance sensors, and we have been able to demonstrate analytically that it is virtually an unbounded value. We describe this approach and submit a complete analytical study demonstrating its unlimited sensing power. To test the approach, we constructed an economical and basic sensor. Despite its simplicity, we demonstrated the discrimination capability to be of the order of 10(-6), as far as we know close to the best sensitivity ever recorded. This detection method is generally applicable to any optical system and may pave the way for the next generation of optical sensing devices.     

Effect of charge transfer state on the exchange interaction of radical-triplet encounter pairs

Chemically induced dynamic electron polarization (CIDEP) of galvinoxyl was measured in various excited molecule-galvinoxyl systems prepared by laser photolysis. Most of the systems examined showed net emission CIDEP, which is well explained by the quartet precursor radical-triplet pair mechanism with exchange interaction,J, of negative sign (quartet is higher than doublet). Several systems with molecules such as naphthalene, quinoxaline, biphenyl and triphenylene, however, showed net absorption CIDEP. Time profiles of CIDEP and kinetic analysis of quenching suggest that net absorption CIDEP is generated during the triplet quenching process by the galvinoxyl radical. We conclude that the net absorption CIDEP is produced during the triplet quenching if theJ value of radical-triplet encounter pair is positive. This is the first report of the radical-triplet encounter pairs with positiveJ value. The mechanism for this unusual positive sign ofJ value is discussed on the basis of the spin-selective configuration interaction between the doublet spin correlated states of radical-triplet and charge transfer encounter pairs.     

Single-molecule reaction and characterization by vibrational excitation

Controlled chemical reaction of single trans-2-butene molecules on the Pd(110) surface was realized by dosing tunneling electrons from the tip of a scanning tunneling microscope at 4.7 K. The reaction product was identified as a 1,3-butadiene molecule by inelastic electron tunneling spectroscopy. Threshold voltage for the reaction is approximately 365 mV, which coincides with the vibrational excitation of the C-H stretching mode. The reaction was ascertained to be caused by C-H bond dissociation by multiple vibrational excitations of the C-H stretching mode via inelastic electron tunneling process.     

A new dual-type DMA for measuring nanoparticles emitted from combustion engines

A new dual-type differential mobility analyzer (dual-type DMA) was developed in order to detect transient number concentrations of airborne nanoparticles with diameters centralized at around 10 nm (for nuclei mode particles) and 100 nm (for accumulation mode particles) in automobile exhaust gas. The apparatus divides the gas sample into two parts, and each part is sent through one of two coaxially nested sections for analysis. For the scanning mode measurement, the nanoparticles are charged by ²⁴¹Am and their size distributions are determined by varying the applied voltage over 2 min. The transient mode measurement, on the other hand, fixes the voltages for the two sections at peaks near 10 and 100 nm in order to monitor the transient behavior of the exhaust nanoparticles. The measurement principles and design of the dual-type DMA are detailed and the results for time response experiments are presented using model nanoparticles charged by a corona charger. The transient concentrations of the nuclei mode and the accumulation mode particles from a diesel engine were shown to be detected by this method, when ²⁴¹Am was used for charging the particles.     

Observation of the D1(2420)-->Dpi + pi- decays

We report on the first observation of D0/1(2420)-->D0pi- pi+ and D+/1(2420-->D+ pi- pi+ decays (where the contribution from the dominant known D1-->D*pi decay mode is excluded) in the B- -->D0/1pi-) and (-)B0-->D+/1pi- decays, respectively. The observation is based on 15.2 x 10(7) B(-)B events collected with the Belle detector at the KEKB collider. We also set 90% confidence level upper limits for the branching fractions of the four following decays: B- -->D0/1pi-, D01-->D(*0)pi- pi+, (-)B0-->D+/1pi-, D+/1-->D(*+) pi- pi+, B- -->D(*0)2(2460)pi-, D(*0)2 -->D(*0) pi- pi+, (-)B0-->D(*+)2(2460)pi-, D(*+)2-->D(*+)pi- pi+.     

Observation of a near-threshold omegaJ/psi mass enhancement in exclusive B-->KomegaJ/psi decays

We report the observation of a near-threshold enhancement in the omegaJ/psi invariant mass distribution for exclusive B-->KomegaJ/psi decays. The results are obtained from a 253 fb(-1) data sample that contains 275 x 10(6) BB pairs that were collected near the Upsilon(4S) resonance with the Belle detector at the KEKB asymmetric energy e(+)e(-) collider. The statistical significance of the omegaJ/psi mass enhancement is estimated to be greater than 8sigma.     

Search for D0-D0 mixing in D0 --> K+ pi(-) decays and measurement of the doubly-Cabibbo-suppressed decay rate

We have searched for mixing in the D(0)-D (0) system by measuring the decay-time distribution of D(0) --> K(+) pi(-) decays. The analysis uses 90 fb(-1) of data collected by the Belle detector at the KEKB e(+) e(-) collider. We fit the decay-time distribution for the mixing parameters x' and y' and also for the parameter R(D), which is the ratio of the rate for the doubly-Cabibbo-suppressed decay D(0)--> K+ pi(-) to that for the Cabibbo-favored decay D(0)--> K-pi(+). We do these fits both assuming CP conservation and allowing for CP violation. We use a frequentist method to obtain a 95% C.L. region in the x'(2) - y' plane. Assuming no mixing, we measure R(D) = (0.381 +/- 0.017(+0.008)(-0.016))%.