Self-Limited Growth of a Thin Oxide Layer on Rh(111)Gustafson, J; Mikkelsen, A; Borg, M; Lundgren, E; Köhler, L; Kresse, G; Schmid, M; Varga, P; Yuhara, J; Torrelles, X; Quirós, C; Andersen, J. N
doi: 10.1103/PhysRevLett.92.126102pmid: 15089690
The oxidation of the Rh(111) surface at oxygen pressures from 10 - 10 mbar to 0.5 bar and temperatures between 300 and 900 K has been studied on the atomic scale using a multimethod approach of experimental and theoretical techniques. Oxidation starts at the steps, resulting in a trilayer O-Rh-O surface oxide which, although not thermodynamically stable, prevents further oxidation at intermediate pressures. A thick corundum like Rh 2 O 3 bulk oxide is formed only at significantly higher pressures and temperatures.
Nanoscale Phase Coexistence and Percolative Quantum TransportKumar, Sanjeev ; Majumdar, Pinaki
doi: 10.1103/PhysRevLett.92.126602pmid: 15089694
We study the nanoscale phase coexistence of ferromagnetic metallic and antiferromagnetic insulating (AFI) regions by including the effect of AF superexchange and weak disorder in the double exchange model. We use a new Monte Carlo technique, mapping on the disordered spin-fermion problem to an ef<?format ?>fective short range spin model, with self-consistently computed exchange constants. We recover “clus<?format ?>ter coexistence” as seen earlier in exact simulation of small systems. The much larger sizes, ∼ 32 × 32 , accessible with our technique, allow us to study the cluster pattern for varying electron density, disorder, and temperature. We track the magnetic structure, obtain the density of states, with its “pseudogap” features, and, for the first time, provide a fully microscopic estimate of the resistivity in a phase coexistence regime, comparing it with the “percolation” scenario.
Femtosecond Coincidence Imaging of Multichannel Multiphoton DynamicsRijs, Anouk M; Janssen, Maurice H
doi: 10.1103/PhysRevLett.92.123002pmid: 15089669
The novel technique of femtosecond time-resolved photoelectron-photoion coincidence imaging is applied to unravel dissociative ionization processes in a polyatomic molecule. Femtosecond coincidence imaging of CF 3 I photodynamics illustrates how competing multiphoton dissociation pathways can be distinguished, which would be impossible using photoelectron or ion imaging alone. Ion-electron energy correlations and photoelectron angular distributions reveal competing processes for the channel producing ( e - + CF 3 + + I ). The molecular-frame photoelectron angular distributions of the two major pathways are strikingly different.