Untersuchung der Milch

Ohne Zusammenfassung     

In situ femtosecond spectroelectrochemistry of Au(1 1 1) in an aqueous chloride solution

In this paper we report the first in situ femtosecond spectroelectrochemistry experiment employing a broadband probe, allowing the measurement of ultrafast transient visible spectra with a fixed pump wavelength. We investigated in situ femtosecond transient reflectivity of a Au(1 1 1) electrode in contact with an aqueous KCl solution. The pump wavelength was set at 780 nm and a supercontinuum probe was employed, yielding ultrafast spectral information on the electron thermalisation dynamics in the range 450–650 nm. Electrochemical control allowed to investigate the dynamic response to different Cl^? adsorption conditions.     

A radiation condition for uniqueness in a wave propagation problem for 2‐D open waveguides

We study the uniqueness of solutions of Helmholtz equation for a problem that concerns wave propagation in waveguides. The classical radiation condition does not apply to our problem because the inhomogeneity of the index of refraction extends to infinity in one direction. Also, because of the presence of a waveguide, some waves propagate in one direction with different propagation constants and without decaying in amplitude. We provide an explicit condition for uniqueness for rectilinear waveguides, which takes into account the physically significant components, corresponding to guided and non‐guided waves; this condition reduces to the classical Sommerfeld–Rellich condition in the relevant cases. By a careful asymptotic analysis we prove that the solution derived by Magnanini and Santosa (SIAM J. Appl. Math. 2001; 61 :1237–1252) for stratified media satisfies our radiation condition. Copyright © 2008 John Wiley & Sons, Ltd.     

Solvent-dependent activation of intermediate excited states in the energy relaxation pathways of spheroidene

In carotenoids internal conversion between the allowed (S(2)) and forbidden (S(1)) excited states occurs on a sub-picosecond timescale; the involvement of an intermediate excited state(s) (S(x)) mediating the process is controversial. Here we use high time resolution (sub-20 fs) broadband (1.2-2.5 eV) pump-probe spectroscopy to study the solvent dependence of excited state dynamics of spheroidene, a naturally-occurring carotenoid with ten conjugated double bonds. In the high polarizability solvent, CS(2), we find no evidence of an intermediate state, and the traditional three-level (S(0), S(1), S(2)) model fully accounts for the S(2)→ S(1) process. On the other hand, in the low polarizability solvent, cyclohexane, we find that rapid (~30 fs) relaxation to an intermediate state, S(x), lying between S(1) and S(2) is required to account for the data. We interpret these results as due to a shift of the S(2) energy, which positions the state above or below the energy of S(x) in response to changes in solvent polarizability.