Molecular orbital study of co chemisorption and oxidation on a Pt(111) surface

A molecular orbital study was made, using an atom superposition and electron delocalization (ASED) technique, of the structures and energy levels of CO on Pt(111) surface. CO is predicted to be preferentially adsorbed at a height of 2.05 Å from the surface at a 1-fold position with the carbon end down. The calculated binding energy (1.7 eV) is in good agreement with the recent experimental result (1.5 eV) of Campbell et al. Calculated binding energies for bridging (1.3 eV) and high coordinate (1.1 eV) sites are predicted to be smaller in magnitude. Calculated results are used to discuss the ordering of energy levels of adsorbed CO. The interaction between CO (adsorbed) and O (adsorbed) has been studied to estimate the energy of activation for the oxidation of CO on Pt(111) surface. The calculated activation energy (1.6 eV) is in reasonable agreement with the recent experimental result (1 eV) of Campbell et al. The Langmuir-Hinshelwood mechanism is found to be favored. We predict CO₂ bonds vertically.     

Nonequilibrium dynamics of a diffusion-limited reaction driven by a cluster-memory mechanism

The diffusion-limited reaction A+AA+B is studied in general dimension. The asymptotic decay of the system is found to depend nontrivially upon the initial concentration of A particles for certain ranges of the diffusion constant, backward reaction rate, and total concentration of particles. This nonequilibrium behavior is due to the formation of clusters centered about the initial A particles. A perturbative analysis ind=1 shows that the transition to the nonequilibrium dynamics is sharp and is quite similar to another previously studied reaction A+AA. Ford>1, a scaling argument is presented which describes the dependence of the asymptotic decay on the initial concentration of A particles and the equilibrium concentration for large backward reaction rates. Monte Carlo data are shown which confirm the analytic work ind=1, 2, and 3.     

Four-channel coarse WDM for inter- and intra-satellite optical communications

A polymer volume grating-based four-channel coarse wavelength division multiplexer (WDM) for inter- and intra-satellite optical communication application is reported for the first time. This compact four-channel WDM device working at 0.83, 1.06, 1.34 and 1.55 μm is designed to build a complete optical link between two satellites, where wavelengths of 0.83 and 1.55 μm are used for data stream channels, 1.06 and 1.34 μm are used for inter- and intra-satellite connection. It is for the first time reported that a WDM device can cover such a large wavelength range in a single substrate. For transverse electric (TE) wave, the channel efficiencies at 0.83, 1.06, 1.34 and 1.55 μm are 55%, 40%, 35% and 45%, respectively. Channel efficiencies for transverse magnetic (TM) waves are 20% lower than those of TE waves on average. Wavelength shifts due to Doppler effect, temperature variations and radiation effects in space can be adequately accommodated.     

Natural halotrichites—an EDX and Raman spectroscopic study

Raman spectroscopy has been used to characterise four natural halotrichites: halotrichite FeSO₄.Al₂(SO₄)₃. 22H₂O, apjohnite MnSO₄.Al₂(SO₄)₃.22H₂O, pickingerite MgSO₄.Al₂(SO₄)₃.22H₂O and wupatkiite CoSO₄.Al₂(SO₄)₃.22H₂O. A comparison of the Raman spectra is made with the spectra of the equivalent synthetic pseudo‐alums. Energy dispersive X‐ray analysis (EDX) was used to determine the exact composition of the minerals. The Raman spectrum of apjohnite and halotrichite display intense symmetric bands at ∼985 cm⁻¹ assigned to the ν₁(SO₄)²⁻ symmetric stretching mode. For pickingerite and wupatkiite, an intense band at ∼995 cm⁻¹ is observed. A second band is observed for these minerals at 976 cm⁻¹ attributed to a water librational mode The series of bands for apjohnite at 1104, 1078 and 1054 cm⁻¹, for halotrichite at 1106, 1072 and 1049 cm⁻¹, for pickingerite at 1106, 1070 and 1049 cm⁻¹ and for wupatkiite at 1106, 1075 and 1049 cm⁻¹ are attributed to the ν₃(SO₄)²⁻ antisymmetric stretching modes of ν₃(B_g) SO₄. Raman bands at around 474, 460 and 423 cm⁻¹ are attributed to the ν₂(A_g) SO₄ mode. The band at 618 cm⁻¹ is assigned to the ν₄(B_g) SO₄ mode. The splitting of the ν₂, ν₃ and ν₄ modes is attributed to the reduction of symmetry of the SO₄ and it is proposed that the sulphate coordinates to water in the hydrated aluminium in bidentate chelation. Copyright © 2007 John Wiley & Sons, Ltd.     

Solutions of Yang's EuclideanR-gauge equations and self-duality

Under some assumptions and transformations of variables, Yang's equations forR-gauge fields on Euclidean space lead to conformally invariant equations permitting one to obtain infinitely many other solutions from any solution of these conformally invariant equations. These conformally invariant equations closely resemble the mathematically interesting generalized Lund-Regge equations. Some exact solutions of these conformally in variant equations are obtained. Except for some singular situations, these solutions are self-dual.     

Incompressibility of strange matter

Strange stars (ReSS) calculated from a realistic equation of state (EOS), that incorporate chiral symmetry restoration as well as deconfinement at high density [Phys. Lett. B 438 (1998) 123; Phys. Lett. B 447 (1999) 352, Addendum; Phys. Lett. B 467 (1999) 303, Erratum; Indian J. Phys. B 73 (1999) 377] show compact objects in the mass radius curve. We compare our calculations of incompressibility for this EOS with that of nuclear matter. One of the nuclear matter EOS has a continuous transition to ud-matter at about five times normal density. Another nuclear matter EOS incorporates density dependent coupling constants. From a look at the consequent velocity of sound, it is found that the transition to ud-matter seems necessary.