| 1. |
- Chernenk, Kirill, et al.
(författare)
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Performance and characterization of the FinEstBeAMS beamline at the MAX IV Laboratory
- 2021
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Ingår i: Journal of Synchrotron Radiation. - 0909-0495. ; 28, s. 1620-1630
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Tidskriftsartikel (refereegranskat)abstract
- FinEstBeAMS (Finnish-Estonian Beamline for Atmospheric and Materials Sciences) is a multidisciplinary beamline constructed at the 1.5 GeV storage ring of the MAX IV synchrotron facility in Lund, Sweden. The beamline covers an extremely wide photon energy range, 4.5-1300 eV, by utilizing a single elliptically polarizing undulator as a radiation source and a single grazing-incidence plane grating monochromator to disperse the radiation. At photon energies below 70 eV the beamline operation relies on the use of optical and thin-film filters to remove higher-order components from the monochromated radiation. This paper discusses the performance of the beamline, examining such characteristics as the quality of the gratings, photon energy calibration, photon energy resolution, available photon flux, polarization quality and focal spot size.
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| 2. |
- Kuzmin, Mikhail, et al.
(författare)
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Investigation of the structural anisotropy in a self-assembling glycinate layer on Cu(100) by scanning tunneling microscopy and density functional theory calculations
- 2017
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Ingår i: Applied Surface Science. - : Elsevier BV. - 0169-4332 .- 1873-5584. ; 409, s. 111-116
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Tidskriftsartikel (refereegranskat)abstract
- Self-assembling organic molecule-metal interfaces exhibiting free-electron like (FEL) states offers an attractive bottom-up approach to fabricating materials for molecular electronics. Accomplishing this, however, requires detailed understanding of the fundamental driving mechanisms behind the self assembly process. For instance, it is still unresolved as to why the adsorption of glycine ([NH2(CH2)COOH) on isotropic Cu(100) single crystal surface leads, via deprotonation and self-assembly, to a glycinate ([NH2(CH2)COO-]) layer that exhibits anisotropic FEL behavior. Here, we report on bias-dependent scanning tunneling microscopy (STM) experiments and density functional theory (DFT) calculations for glycine adsorption on Cu(100) single crystal surface. We find that after physical vapor deposition (PVD) of glycine on Cu(100), glycinate self-assembles into an overlayer exhibiting c(2 x 4) and p(2 x 4) symmetries with non-identical adsorption sites. Our findings underscore the intricacy of electrical conductivity in nanomolecular organic overlayers and the critical role the structural anisotropy at molecule-metal interface plays in the fabrication of materials for molecular electronics.
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| 3. |
- Ali-Löytty, Harri, et al.
(författare)
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Chemical Dissolution of Pt(111) during Potential Cycling under Negative pH Conditions Studied by Operando X-ray Photoelectron Spectroscopy
- 2019
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Ingår i: The Journal of Physical Chemistry C. - : American Chemical Society (ACS). - 1932-7447 .- 1932-7455. ; 123:41, s. 25128-25134
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Tidskriftsartikel (refereegranskat)abstract
- Dissolution of a platinum catalyst is a major degradation mechanism of fuel cells, but the exact reaction mechanism has remained unclear. Here, electrochemical ambient pressure X-ray photoelectron spectroscopy (EC-APXPS) was utilized to provide direct information on chemical species on a single-crystal Pt(111) electrode under extremely low pH conditions. Measurements were conducted using a novel condensed electrolyte film electrochemical cell applying work function measurement as a loss-free probe for electrochemical potential. We show that platinum can dissolve chemically as Pt2+ ion during potential cycling and redeposit as Pt2+ at the onset potential for cathodic reactions. The dissolution of Pt does not require electrochemical oxidation via oxide place exchange. In contrast, the adsorption of oxygenated species (OH* or O*) at the onset potential for anodic reactions is a sufficient prerequisite to the dissolution. These results provide new insight into the degradation mechanism of Pt under extremely low pH conditions, predicted by the Pourbaix diagram, having practical applications to the durability of Pt-based catalysts in electrochemical energy conversion devices.
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| 4. |
- Ali-Löytty, Harri, et al.
(författare)
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The role of (FeCrSi)2(MoNb)-type Laves phase on the formation of Mn-rich protective oxide scale on ferritic stainless steel
- 2018
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Ingår i: Corrosion Science. - : Elsevier BV. - 0010-938X. ; 132, s. 214-222
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Tidskriftsartikel (refereegranskat)abstract
- Microalloying of stainless steel with reactive elements increases oxidation resistance but makes the alloy prone to microstructural changes. XPS results reveal changes in the initial oxidation mechanism on Ti-Nb stabilized ferritic stainless steel (EN 1.4521) after 120 h heat treatment at 650 °C. Age-precipitation of (FeCrSi)2(MoNb)-type Laves phase resulted in less pronounced surface segregation and oxidation of microalloying elements. Si oxidizes preferentially at the Laves precipitate locations via outward diffusion forming diffusion barrier for the other scale forming elements. Most significantly the diffusion of Mn and the formation of low volatile (Mn,Cr)3O4 spinel oxide at the surface was strongly suppressed.
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| 5. |
- Kooser, Kuno, et al.
(författare)
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Gas-phase endstation of electron, ion and coincidence spectroscopies for diluted samples at the FinEstBeAMS beamline of the MAX IV 1.5 GeV storage ring
- 2020
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Ingår i: Journal of Synchrotron Radiation. - 0909-0495. ; 27, s. 1080-1091
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Tidskriftsartikel (refereegranskat)abstract
- Since spring 2019 an experimental setup consisting of an electron spectrometer and an ion time-of-flight mass spectrometer for diluted samples has been available for users at the FinEstBeAMS beamline of the MAX IV Laboratory in Lund, Sweden. The setup enables users to study the interaction of atoms, molecules, (molecular) microclusters and nanoparticles with short-wavelength (vacuum ultraviolet and X-ray) synchrotron radiation and to follow the electron and nuclear dynamics induced by this interaction. Test measurements of N2 and thiophene (C4H4S) molecules have demonstrated that the setup can be used for many-particle coincidence spectroscopy. The measurements of the Ar 3p photoelectron spectra by linear horizontal and vertical polarization show that angle-resolved experiments can also be performed. The possibility to compare the electron spectroscopic results of diluted samples with solid targets in the case of Co2O3 and Fe2O3 at the Co and Fe L 2,3-absorption edges in the same experimental session is also demonstrated. Because the photon energy range of the FinEstBeAMS beamline extends from 4.4 eV up to 1000 eV, electron, ion and coincidence spectroscopy studies can be executed in a very broad photon energy range.
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| 6. |
- Palmolahti, Lauri, et al.
(författare)
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Pinhole-resistant nanocrystalline rutile TiO2 photoelectrode coatings
- 2022
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Ingår i: Acta Materialia. - : Elsevier BV. - 1359-6454. ; 239
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Tidskriftsartikel (refereegranskat)abstract
- Atomic layer deposited (ALD) TiO2 thin films have a wide range of applications in photonics which are, however, limited by the chemical instability of the amorphous as-deposited TiO2. Post-deposition annealing is required for improving the performance by inducing phase transitions and oxide defects. ALD precursor traces remaining in the TiO2 film affect the thermally-induced processes but the understanding of the effect of growth temperature on precursor traces in the film as well as on the thermally-induced processes is weak. In this study 30 nm ALD TiO2 was grown on Si wafer from tetrakis(dimethylamido)titanium and water at 100–200 °C. TiO2 was subsequently annealed in vacuum at 200–500 °C. Increasing the growth temperature decreased the amount of N bearing precursor traces and thus makes the TiO2 more easily reducible. The reduction takes place simultaneously with the crystallization and formation of O1− defects. Vacuum annealing of TiO2 with less than 0.3 at% of N results in nanocrystalline rutile whereas samples with more N containing traces crystallized as microcrystalline anatase. Nanocrystalline rutile TiO2 was chemically stable and resistant to the dissolution at the grain boundaries under alkaline conditions making it a suitable material for protective photoelectrode coatings used in artificial photosynthesis.
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| 7. |
- Pankratov, Vladimir, et al.
(författare)
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Progress in development of a new luminescence setup at the FinEstBeAMS beamline of the MAX IV laboratory
- 2019
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Ingår i: Radiation Measurements. - : Elsevier BV. - 1350-4487. ; 121, s. 91-98
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Tidskriftsartikel (refereegranskat)abstract
- FinEstBeAMS is a new materials science beamline at the 1.5 GeV storage ring of the MAX IV Laboratory in Lund, Sweden. It has been built based on grazing incidence monochromatization of synchrotron light, which allows to cover a remarkably wide excitation energy range from ultraviolet to soft x-rays (4.5–1450 eV). A new mobile luminescence spectroscopy end station has been commissioned with design benefitting from the advantages of a high flux elliptically polarizing undulator light source. We report on the design of the luminescence end station, its technical realization and performance achieved so far. Special attention is paid to the experimental challenges for luminescence spectroscopy under grazing incidence excitation conditions. The first luminescence results obtained demonstrate a reliable performance of the advanced setup at FinEstBeAMS.
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| 8. |
- Ruoko, Tero-Petri, et al.
(författare)
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Charge carrier dynamics in tantalum oxide overlayered and tantalum doped hematite photoanodes
- 2019
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Ingår i: Journal of Materials Chemistry A. - : ROYAL SOC CHEMISTRY. - 2050-7488 .- 2050-7496. ; 7:7, s. 3206-3215
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Tidskriftsartikel (refereegranskat)abstract
- We employ atomic layer deposition to prepare 50 nm thick hematite photoanodes followed by passivating them with a 0.5 nm thick Ta2O5-overlayer and compare them with samples uniformly doped with the same amount of tantalum. We observe a three-fold improvement in photocurrent with the same onset voltage using Ta-overlayer hematite photoanodes, while electrochemical impedance spectroscopy under visible light irradiation shows a decreased amount of surface states under water splitting conditions. The Tadoped samples have an even higher increase in photocurrent along with a 0.15 V cathodic shift in the onset voltage and decreased resistivity. However, the surface state capacitance for the Ta-doped sample is twice that of the reference photoanode, which implies a larger amount of surface hole accumulation. We further utilize transient absorption spectroscopy in the sub-millisecond to second timescale under operating conditions to show that electron trapping in both Ta2O5-passivated and Ta-doped samples is markedly reduced. Ultrafast transient absorption spectroscopy in the sub-picosecond to nanosecond timescale shows faster charge carrier dynamics and reduced recombination in the Ta-doped hematite photoanode resulting in the increased photoelectrochemical performance when compared with the Ta2O5-overlayer sample. Our results show that passivation does not affect the poor charge carrier dynamics intrinsic to hematite based photoanodes. The Ta-doping strategy results in more efficient electron extraction, solving the electron trapping issue and leading to increased performance over the surface passivation strategy.
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| 9. |
- Saari, Jesse, et al.
(författare)
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Tunable Ti 3+ -Mediated Charge Carrier Dynamics of Atomic Layer Deposition-Grown Amorphous TiO 2
- 2022
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Ingår i: Journal of Physical Chemistry C. - : American Chemical Society (ACS). - 1932-7447 .- 1932-7455. ; 126:9, s. 4542-4554
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Tidskriftsartikel (refereegranskat)abstract
- Amorphous titania (am.-TiO2) has gained wide interest in the field of photocatalysis, thanks to exceptional disorder-mediated optical and electrical properties compared to crystalline TiO2. Here, we study the effects of intrinsic Ti3+ and nitrogen defects in am.-TiO2 thin films via the atomic layer deposition (ALD) chemistry of tetrakis(dimethylamido)titanium(IV) (TDMAT) and H2O precursors at growth temperatures of 100-200 °C. X-ray photoelectron spectroscopy (XPS) and computational analysis allow us to identify structural disorder-induced penta- and heptacoordinated Ti4+ ions (Ti5/7c4+), which are related to the formation of Ti3+ defects in am.-TiO2. The Ti3+-rich ALD-grown am.-TiO2 has stoichiometric composition, which is explained by the formation of interstitial peroxo species with oxygen vacancies. The occupation of Ti3+ 3d in-gap states increases with the ALD growth temperature, inducing both visible-light absorption and electrical conductivity via the polaron hopping mechanism. At 200 °C, the in-gap states become fully occupied extending the lifetime of photoexcited charge carriers from the picosecond to the nanosecond time domain. Nitrogen traces from the TDMAT precursor had no effect on optical properties and only little on charge transfer properties. These results provide insights into the charge transfer properties of ALD-grown am.-TiO2 that are essential to the performance of protective photoelectrode coatings in photoelectrochemical solar fuel reactors.
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| 10. |
- Vuori, Leena, et al.
(författare)
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Improved corrosion properties of hot dip galvanized steel by nanomolecular silane layers as hybrid interface between zinc and top coatings
- 2017
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Ingår i: Corrosion: Journal of science and engineering. - : NACE International. - 0010-9312. ; 73:2, s. 169-180
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Tidskriftsartikel (refereegranskat)abstract
- Thin organic coatings (TOC) or paints on hot dip galvanized steel (HDGS) improve the corrosion properties and create visually pleasing surfaces. Delamination of these coatings leads to corrosion and peeling of the paints. Hence, a novel method for improved adhesion and corrosion properties for HDGS surfaces is introduced. It is shown how the fabrication of a nanomolecular silane film as an interfacial layer between the HDGS and TOC or paint improves the corrosion properties of HDGS in different pH regimes. Understanding the corrosion behavior of ultra-thin silane layers under differing pH is crucial, as subsequent coatings have different pHs. By varying the silanization parameters, two different nanomolecular surface structures of aminopropyl trimethoxysilane (APS) on HDGS were fabricated: well-ordered monolayers with approximately 1 nm thickness and highly clustered APS films with a thickness in the range of 5 nm to 8 nm. To verify the nanomolecular APS structures, photoelectron spectroscopy and contact angle measurements were used. The corrosion properties of HDGS and silanized HDGS were studied with linear sweep voltammetry and electrochemical impedance spectroscopy. It is shown that at pH 5 and 7, passivation behavior is observed on silanized samples, but the most significant improvement in corrosion resistance is found at pH 10, where the corrosion currents of silanized samples are up to two orders of magnitude lower than on uncoated metallic samples. Also, it is demonstrated that the corrosion inhibition of APS is not only dependent on the thickness of the silane film, but also the molecular ordering at the surface. The thin, well-ordered APS monolayer is more resistant toward corrosion in NaCl solution (pH 7) than thicker clustered APS layer. This indicates that the highly ordered nanomolecular surface structure protects the HDGS/silane interface from the Cl- adsorption better than the thicker, but more randomly ordered, APS layers. Nanomolecular interfacial silane films for enhanced corrosion and adhesion properties on HDGS are transferrable to industrial production lines providing a low cost and environmentally friendly method for improved HDGS products.
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