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We investigate femtosecond-laser induced desorption [desorption induced by multiple electronic transitions (DIMET)] of NO molecules from thin Pt(111) films. On the basis of a two-state, open-system density matrix treatment in combination with a two-temperature model, we argue that decreasing the film thickness enhances desorption cross sections by orders of magnitude in comparison to bulk materials. Both the spatial confinement and the laser fluence appear therefore as efficient, nonlinear enhancement factors for nonadiabatic photoreactions of metal surfaces and, possibly, of nanostructered materials in general
We propose an optical ring interferometer to observe environment-induced spatial decoherence of massive objects. The object is held in a harmonic trap and scatters light between degenerate modes of a ring cavity. The output signal of the interferometer permits to monitor the spatial width of the object's wave function. It shows oscillations that arise from coherences between energy eigenstates and that reveal the difference between pure spatial decoherence and that coinciding with energy transfer and heating. Our method is designed to work with a wide variety of masses, ranging from the atomic scale to nanofabricated structures. We give a thorough discussion of its experimental feasibility