| 1. |
- Pärna, R., et al.
(författare)
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FinEstBeaMS – A wide-range Finnish-Estonian Beamline for Materials Science at the 1.5 GeV storage ring at the MAX IV Laboratory
- 2017
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Ingår i: Nuclear Instruments and Methods in Physics Research, Section A: Accelerators, Spectrometers, Detectors and Associated Equipment. - : Elsevier BV. - 0168-9002. ; 859, s. 83-89
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Tidskriftsartikel (refereegranskat)abstract
- The FinEstBeaMS beamline is under construction at the 1.5 GeV storage ring of the MAX IV Laboratory at Lund, Sweden. It has been designed to cover an unusually wide energy range from ultraviolet (4.3 eV) to soft X-rays (1000 eV) but experiments will also be possible at the Mg and Al Kα energies. Instead of having two different insertion devices and optical schemes for low and high photon energy regions, we have based our design on a single long-period, elliptically polarizing undulator and a plane grating monochromator. This solution will provide very good conditions for planned experiments in the whole photon energy region. The beamline will have two branches: one will mainly be used to investigate free atoms, molecules and clusters with photoelectron/photoion coincidence spectroscopy as well as solids with photoluminescence spectroscopy whereas the other one will be dedicated to ultra-high vacuum studies of surfaces and interfaces, utilizing X-ray photoelectron spectroscopy and X-ray absorption spectroscopy. This paper focuses on the optical design of the beamline and general design concepts of the gas phase and solid state end stations.
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| 2. |
- Andersson, T., et al.
(författare)
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Electronic structure transformation in small bare Au clusters as seen by x-ray photoelectron spectroscopy
- 2017
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Ingår i: Journal of Physics B. - : IOP Publishing. - 0953-4075 .- 1361-6455. ; 50:1
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Tidskriftsartikel (refereegranskat)abstract
- Free bare gold clusters in the size range from few tens to few hundred atoms (<= 1 nm dimensions) have been produced in a beam, and the size-dependent development of their full valence band including the 5d and 6s parts has been mapped 'on the fly' by synchrotron-based photoelectron spectroscopy. The Au 4f core level has been also probed, and the cluster-specific Au 4f ionization energies have been used to estimate the cluster size. The recorded in the present work valence spectra of the small clusters are compared with the spectra of the large clusters (N similar to 10(3)) created by us using a magnetron-based gas aggregation source. The comparison shows a substantially narrower 5d valence band and the decrease in its splitting for gold clusters in the size range of few hundred atoms and below. Our DFT calculations involving the pseudopotential method show that the 5d band width of the ground state increases with the cluster size and by the size N = 20 becomes comparable with the experimental width of the valence photoelectron spectrum. Similar to the earlier observations on supported clusters we interpret our experimental and theoretical results as due to the undercoordination of a large fraction of atoms in the clusters with N similar to 10(2) and below. The consequences of such electronic structure of small gold clusters are discussed in connection with their specific physical and chemical properties related to nanoplasmonics and nanocatalysis.
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| 3. |
- Hautala, Lauri, et al.
(författare)
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Experimental observation of structural phase transition in CsBr clusters
- 2017
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Ingår i: Physical Review B. - 1098-0121. ; 95:4
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Tidskriftsartikel (refereegranskat)abstract
- Formation and growth of CsBr clusters embedded in unsupported Ar clusters was studied using synchrotron radiation photoelectron spectroscopy. The development of the core-level electronic structure for cluster sizes between a few and a few hundred atoms contained information about the local coordination of the constituent particles. The experimental results indicate that a gradual structural phase transition from NaCl structure to CsCl structure for CsBr clusters takes place at around 160 atoms per cluster.
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| 4. |
- Piancastelli, Maria Novella, et al.
(författare)
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X-ray versus Auger emission following Xe 1s photoionization
- 2017
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Ingår i: Physical Review A. Atomic, Molecular, and Optical Physics. - 1050-2947 .- 1094-1622. ; 95:6
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Tidskriftsartikel (refereegranskat)abstract
- Xe 1s photoelectron spectra were measured at SPring-8, Japan. The core-hole lifetime broadening was found to be 9.6 eV, yielding a lifetime of similar to 68 as. The amount of radiative versus nonradiative decay was assessed by recording Auger LMM spectra below and above the K edge. Below the K edge, L vacancies are produced only by direct photoionization, while above the K edge some of these vacancies are mainly produced by KL emission following 1s photoionization. Due to the dipole selection rule for x-ray emission, the dominant role of the KL relaxation process is rather directly observed.
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| 5. |
- Shi, X., et al.
(författare)
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Quantitative assessment of structural and compositional colors induced by femtosecond laser : A case study on 301LN stainless steel surface
- 2019
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Ingår i: Applied Surface Science. - : Elsevier B.V.. - 0169-4332 .- 1873-5584. ; 484, s. 655-662
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Tidskriftsartikel (refereegranskat)abstract
- The topic of durable coloration and passivation of metal surfaces using state-of-the-art techniques has gained enormous attention and devotion with unremitting efforts of researchers worldwide. Although femtosecond laser marking has been performed on many metals, the related coloration mechanisms are mainly referred to structural colors produced by the interaction of visible light with periodic surface structures. Yet, general quantitative determination of the resulting colors and their origins remain elusive. In this work, we realized quantitative separations of structural colors and compositional pigmentary colors on 301LN austenitic stainless steel surfaces that were treated by femtosecond laser machining. The overall color information was extracted from surface reflectance, with structural color given by numerical simulations, and oxide compositions by chemical state analysis. It was shown that the laser-induced apparent colors of 301LN steel surfaces were combinations of structural and compositional colorations, with the former dominating the angular response and the latter setting up the brownish bases. In addition to the quantification of colors, the analysis method in this work may be useful for the generation and specification of tailored color palettes for practical coloration on metal surfaces by femtosecond laser marking.
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| 6. |
- Ceolin, D., et al.
(författare)
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Auger resonant-Raman study at the Ar K edge as probe of electronic-state-lifetime interferences
- 2015
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Ingår i: Physical Review A. Atomic, Molecular, and Optical Physics. - 1050-2947 .- 1094-1622. ; 91:2
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Tidskriftsartikel (refereegranskat)abstract
- The resonant-Auger decay in argon following Ar 1s - np excitations was studied under resonant-Raman conditions, i.e., with a total instrumental bandwidth much narrower than the natural linewidth of the absorption features. These state-of-the-art experiments are combined with a radiationless resonant-Raman scattering theory. The main results include identification of the energy position of some high-lying Rydberg states previously masked by insufficient resolution and clear evidence of electronic-state-lifetime interference phenomena.
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| 7. |
- Kokkonen, E., et al.
(författare)
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Formation of stable HCl+ following resonant Auger decay in CH3Cl
- 2016
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Ingår i: PHYSICAL REVIEW A. - : American Physical Society. - 2469-9926. ; 94:3
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Tidskriftsartikel (refereegranskat)abstract
- Photoinduced reformation of chemical bonds is investigated in the CH3Cl molecule experimentally and computationally. The observation of stable HCl+ fragment formation after resonant Cl 2p photoexcitation is confirmed by an electron-ion coincidence experiment, and its possible creation mechanism is reported. We attribute the formation of HCl+ to specific final states populated by the resonant Auger decay. Quantum chemical computations support this attribution and suggest that in at least one of those states the system is placed on a potential energy surface which favors creation of HCl+ by moving one hydrogen atom to a closer proximity of the chlorine atom. This work demonstrates the effect of targeted core-shell excitation on the chemical bond breaking and reformation process, often called photoinduced chemistry.
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| 8. |
- Huotari, J., et al.
(författare)
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Separation of valence states in thin films with mixed V2O5 and V7O16 phases
- 2016
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Ingår i: Journal of Electron Spectroscopy and Related Phenomena. - : Elsevier BV. - 0368-2048 .- 1873-2526. ; 211, s. 47-54
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Tidskriftsartikel (refereegranskat)abstract
- Among the other applications, vanadium oxide thin films are considered to be excellent candidates for gas sensing. To understand the origins of the sensing capability, we carried out X-ray photoelectron and X-ray absorption spectroscopy measurements to determinate the surface valence states of thin films with mixed V7O16 and V2O5 compounds. Thin films were fabricated by pulsed laser deposition, and the crystal structure and symmetry of the deposited films was studied using grazing incidence X-ray diffraction and Raman spectroscopy. These results together with X-ray photoelectron and absorption spectra showed that the thin-film crystal structures varied between orthorhombic V2O5 phase and another phase of triclinic V7O16. X-ray photoelectron spectroscopy was used to quantitatively confirm the high amount of V4+ ions on surfaces of the films, especially of films with V7O16 phase present. This result was confirmed in the quantitative analysis of the V2p near-edge X-ray absorption spectra. Through the observed electronic structures, it was found that in addition to unique crystal structure and morphology, the enhanced gas sensitivity of these layers is attributed to the increase in the amount of surface oxygen vacancies.
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| 9. |
- Kokkonen, E., et al.
(författare)
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Fragmentation of mercury compounds under ultraviolet light irradiation
- 2015
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Ingår i: Journal of Chemical Physics. - : AIP Publishing. - 0021-9606 .- 1089-7690. ; 143:7
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Tidskriftsartikel (refereegranskat)abstract
- Ultraviolet light induced photofragmentation of mercury compounds is studied experimentally with electron energy resolved photoelectron-photoion coincidence techniques and theoretically with computational quantum chemical methods. A high resolution photoelectron spectrum using synchrotron radiation is presented. Fragmentation of the molecule is studied subsequent to ionization to the atomic-mercury-like d orbitals. State dependent fragmentation behaviour is presented and specific reactions for dissociation pathways are given. The fragmentation is found to differ distinctly in similar orbitals of different mercury compounds.
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