Optical pseudomotors for soft x-ray beamlines.

Optical elements of soft x-ray beamlines usually have motorized translations and rotations that allow for the fine alignment of the beamline. This is to steer the photon beam at some positions and to correct the focus on slits or on sample. Generally, each degree of freedom of a mirror induces a change of several parameters of the beam. Inversely, several motions are required to actuate on a single optical parameter, keeping the others unchanged. We define optical pseudomotors as combinations of physical motions of the optical elements of a beamline, which allow modifying one optical parameter without affecting the others. We describe a method to obtain analytic relationships between physical motions of mirrors and the corresponding variations of the beam parameters. This method has been implemented and tested at two beamlines at ALBA, where it is used to control the focus of the photon beam and its position independently.

Electronic structure of C60 on Au(887).

We present an analysis of the electronic structure of C60 adsorbed on a vicinal Au(111) surface at different fullerene coverages using photoemission, x-ray absorption, and scanning tunneling microscopy/spectroscopy (STS). STS provides a straightforward determination of the highest occupied molecular orbital (HOMO) and the lowest unoccupied molecular orbital (LUMO) levels with respect to the Fermi energy. At C60 coverages of 0.5 and 1 ML a 2.7 eV wide HOMO-LUMO gap is found. The near-edge x-ray absorption fine structure (NEXAFS) spectrum for the 0.5 ML C60 nanomesh structure displays a significant intensity at the low energy side of the LUMO exciton peak, which is explained as due to absorption into HOMO-LUMO gap states localized at individual C60 cluster edges. From 0.5 to 1 ML we observe a rigid shift of the HOMO-LUMO peaks in the STS spectra and an almost complete quenching of the gap states feature in NEXAFS.

Nucleobase orientation and ordering in films of single-stranded DNA on gold.

We demonstrate how the orientation and ordering of DNA bases in ultrahigh vacuum (UHV) and ambient environments can be determined using complementary spectroscopic methods. Near-edge X-ray absorption fine structure (NEXAFS) with fluorescence detection, X-ray photoelectron (XPS), and Fourier transform infrared (FTIR) spectroscopies are used to quantify the coverage, chemical composition, orientation, and ordering of thymine bases in model self-assembled monolayers of thymine homo-oligonucleotides [oligo(dT)] on gold. We find that, in monolayers of thiol-modified oligo(dT), thymine bases tend to orient parallel to the Au substrate, and this preferential orientation is significantly more pronounced in monolayers of thiolated 5-mers compared to 25-mers. We interpret this preferential orientation as a signature of significant correlations (local ordering) between individual nuleobases, which offers a way to quantify and compare nucleobase interactions in films under both ambient and UHV conditions.

Electron confinement in surface states on a stepped gold surface revealed by angle-resolved photoemission.

STM images show that vicinal Au(788) surfaces are made up of a uniform array of (111)-oriented terraces of similar width ( approximately 3.8 nm). This uniformity makes it possible to study the electronic structure of the resulting step superlattice by angle-resolved photoemission. We show that for this terrace array the surface state appears to be broken up into one-dimensional quantum-well levels, indicating total electron confinement within the terraces. The angular resolution allows the probability density of the terrace quantum well state to be mapped in reciprocal space, complementing nicely the wave function measured in real space by STM.

A study of the response of Y3Al5O12:Ce phosphor powder screens in the vacuum ultraviolet and soft X-ray regions using synchrotron radiation.

Phosphor screens find application in many fields because of their ability to convert incident radiation to wavelengths that are readily measured by modern detectors. While the response of such screens in the X-ray region has been widely studied, much work still remains to be done regarding their response in the vacuum ultraviolet and soft X-ray regions, where the response is predicted to be non-linear owing to the presence of elemental absorption edges. Here, an experiment using synchrotron radiation to determine the response of thin Y(3)Al(5)O(12):Ce (1-21 mg cm(-2)) and Y(2)O(3):Eu (2.64 mg cm(-2)) powder phosphor screens in the spectral range 20-900 A (13.8-620 eV) is reported. Also, a custom-built camera is described which permits simultaneous collection of the forward- and backward-emitted light and that enables measurements to be made at various positions across the screens and at several screen/incident beam angles. Finally, features in the response spectra are identified, and efficiencies across the spectral range indicated for different screen thicknesses and operating modes are plotted, before a curve of the intrinsic radiant efficiency of Y(3)Al(5)O(12):Ce is produced. The results are discussed in the context of other measurements.