This paper reviews aspects of nonlinear optical spectroscopy of interfaces. The emphasis is put on second-order nonlinear optical techniques, such as sum-frequency generation (SFG), which possess intrinsic surface or interface selectivity and can therefore be used to probe buried interfaces accessible by light. The basic concepts of the second-order nonlinear response of surfaces and interfaces are given. While SFG in the ultraviolet-visible range allows one to achieve surface-specific electronic spectroscopy, infrared-visible SFG spectroscopy allows one to have access to absolute vibrational spectra of adsorbates at an interface. The main experimental schemes commonly employed are described. Selected experimental examples are given for studies of liquid surfaces and interfaces, polymer surfaces and interfaces, solid surfaces under ultra-high vacuum conditions or in inert atmospheres, solid-gas interfaces, solid-liquid interfaces and solid-solid interfaces. Both frequency-resolved studies and time-domain measurements are addressed.

The self-assembly of the rodlike two-dimensional chiral molecule 4-[trans-2-(pyrid-4-yl-vinyl)] benzoic acid on the Cu(100) surface has been investigated by scanning tunneling microscopy. Upon adsorption at T>or=300 K, the molecules are deprotonated and assemble in parquet patterns when the coverage remains below a critical value. Corresponding high-resolution data reveal that the ordering implies mesoscopic chiral resolution as a result of chiroselective interactions (i.e., two domains comprise exclusively one enantiomer). When the critical coverage is exceeded, an abrupt transition to a single racemic phase is observed with a different lateral molecular coupling scheme. The shifting of the subtle balance between the weak lateral coupling, substrate bonding, and the packing requirements encountered with the increased molecular coverage is suggested to be the driving force for this homochiral-to-heterochiral phase transition.

We report a comparative study on the 2D self-assembly of two related ditopic benzoic acid species, which have similar shape and endgroups but different backbone symmetry. High-resolution scanning tunneling microscopy data reveal how the symmetry information of molecular building blocks is readily expressed in the resulting chiral or nonchiral supramolecular networks. The underlying square Cu(100) surface steers network orientation and accounts for carboxylate formation, resulting in an unusual intermolecular hydrogen bond motif. Our results demonstrate that symmetry and chiral resolution in 2D supramolecular assembly can be controlled via the design of functional molecules and choice of substrate.

The authors report ferromagnetism at room temperature in Co doped CeO2−δ thin films grown by pulsed laser deposition on SrTiO3 and Si substrates. On SrTiO3 ceria is epitaxied and displays a high crystalline quality. On Si the films are textured with a dominant orientation. While the ferromagnetism is little affected by the amounts of structural defects, it depends sensitively on the oxygen pressure during growth and annealing. This indicates that oxygen vacancies could be involved in the magnetic coupling between Co ions. Furthermore, the epilayers grown on SrTiO3 display a large magnetic anisotropy with an out of plane easy axis.

The advent of free-electron laser (FEL) sources delivering two synchronized pulses of different wavelengths (or colours) has made available a whole range of novel pump–probe experiments. This communication describes a major step forward using a new configuration of the FERMI FEL-seeded source to deliver two pulses with different wavelengths, each tunable independently over a broad spectral range with adjustable time delay. The FEL scheme makes use of two seed laser beams of different wavelengths and of a split radiator section to generate two extreme ultraviolet pulses from distinct portions of the same electron bunch. The tunability range of this new two-colour source meets the requirements of double-resonant FEL pump/FEL probe time-resolved studies. We demonstrate its performance in a proof-of-principle magnetic scattering experiment in Fe–Ni compounds, by tuning the FEL wavelengths to the Fe and Ni 3p resonances.

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By using heteroepitaxy on two different GaAs templates, we have investigated the impact of anisotropic strain on the magnetocaloric effect (MCE) of MnAs. The temperature range, spread around room temperature, and the maximal MCE position are markedly different in the two epitaxial systems. Simulated MCE curves, obtained from a model based on the mean-field approximation, are in good agreement with the experimental data, indicating that the entropy variation is magnetic in origin. These results illustrate how strain can be used to tune the MCE in materials with coupled structural and magnetic phase transition and suggest that the MCE of MnAs may find applications in microelectronic circuitry.

This article discusses different approaches to build up supramolecular nanoarchitectures on surfaces, which were simultaneously investigated by scanning tunneling microscopy (STM) on the single-molecule level. Following this general road map, first, the hydrogen-bonding guided self-assembly of two different, structural-equivalent molecular building blocks, azobenzene dicarboxylic acid and stilbene dicarboxylic acid, was studied. Secondly, the coordination chemistry of the same building blocks, now acting as ligands in metal coordination reactions, towards co-sublimed Fe atoms was studied under near surface-conditions. Extended two-dimensional tetragonal network formation with unusual Fe2L(4/2)-dimers at the crossing points was observed on copper surfaces. Complementary to the first two experiments, a two-step approach based on the solution-based self-assembly of square-like tetranuclear complexes of the M4L4-type with subsequent deposition on graphite surfaces was investigated. One- and two-dimensional arrangements as well as single molecules of the M4L4-complexes could be observed. Moreover, the local electronic properties of a single M4L4-complexes could be probed with submolecular resolution by means of scanning tunnelling spectroscopy (STS).