Vibrational entropy of L12 Cu3Au measured by inelastic neutron scattering

The phonon density of states of elemental Au, Cu, and Cu3Au with L12 chemical order were measured by inelastic neutron scattering and used to calculate the vibrational entropy of formation of the ordered compound from the elemental metals. A vibrational entropy of formation of (0.06±0.03) kB/atom at 300 K was obtained, with the vibrational entropy of the ordered alloy being larger than that of the elemental metals. The phonon DOS of the disordered Cu3Au was simulated by adding the phonon DOS curves of fcc Cu, L12 Cu3Au, and fcc Au to match the numbers of first-nearest-neighbor pairs in a disordered alloy. The vibrational entropy obtained with this simulated DOS disagrees with calorimetric data and theoretical estimates, indicating that the phonon DOS of disordered Cu3Au depends on chemical order at spatial lengths larger than is set by first-nearest-neighbor pairs

Phonon entropy of alloying and ordering of Cu-Au

Inelastic neutron scattering spectra were measured with a time-of-flight spectrometer on six disordered Cu-Au alloys at 300 K. The neutron-weighted phonon density of states was obtained from a conventional analysis of these spectra. Several methods were developed to account for this neutron weighting and obtain the phonon entropy of the disordered alloys. The phonon entropies of formation of disordered fcc Cu-Au alloys obtained in this way were generally mutually consistent, and were also consistent with predictions from a cluster approximation obtained from ab-initio calculations by Ozolin[underaccent cedilla [below] s-breve, Wolverton, and Zunger. We estimate a phonon entropy of disordering of 0.15±0.05kB/atom in Cu3Au at 300 K. A resonance mode associated with the motions of the heavy Au atoms in the Cu-rich alloys was observed at 9 meV. An analysis of the resonance mode provided a check on the partial phonon entropy of Au atoms

Temperature dependence of the phonon entropy of vanadium

The phonon density-of-states (DOS) of elemental vanadium was measured at elevated temperatures by inelastic neutron scattering. The phonon softening predicted by thermal expansion against the bulk modulus is much larger than the measured shifts in phonon energies. We conclude that the phonon anharmonicities associated with thermal expansion are largely canceled by effects from phonon-phonon scattering. Prior measurements of the heat capacity and calculations of the electronic entropy of vanadium are assessed, and consistency requires an explicit temperature dependence of the phonon DOS. Using data from the literature, similar results are found for chromium, niobium, titanium, and zirconium

Evaluation of electrodeposited alpha Mn2O3 as a catalyst for the Oxygen Evolution Reaction

alpha Mn2O3 is of interest as a low cost and environmentally benign electrocatalyst for the Oxygen Evolution Reaction OER in the process of water splitting. Mechanically stable alpha Mn2O3 electrodes are prepared by annealing of galvanostatically deposited MnOOHx layers on F SnO2 coated glass. The overpotential eta to achieve a current density of j 10 mA cm2 decreases from 590 to 340 mV with increasing layer thickness. Differential capacitance measurements reveal that this high OER activity can be attributed to the large electrochemically active surface area ECSA , which scales linearly with the thickness of these highly porous and electrolyte permeable films. The oxide layers exhibit a reversible oxidation behavior from Mn III to Mn IV , whereas only about 25 of the Mn III is oxidized to Mn IV before the OER reaction takes off. Although the intrinsic activity is small compared to that of other OER catalysts, such as NiFeOx, the combination of high ECSA and good electrical conductivity of these amp; 945; Mn2O3 films ensures that high OER activities can be obtained. The films are found to be stable for gt;2 h in alkaline conditions, as long as the potential does not exceed the corrosion potential of 1.7 V vs. RHE. These findings show that amp; 945; Mn2O3 is a promising OER catalyst for water splitting device

Lasten omaishoitajien kuntoutustarve

Omaisten auttaminen on Suomessa paljon yleisempää kuin mitä omaishoidon tukea saavien määrästä voi päätellä. Erityisesti lastaan hoitavien omaishoitajien määrästä ja tuen tarpeesta on vain vähän tietoa. Kela on uudistamassa omaishoitajille kohdennettuja kursseja. Tämän selvityksen tavoitteena oli kartoittaa lapsia hoitavien lääkäreiden käsitystä siitä, tulisiko lasten omaishoitajille järjestää omat kurssit, kuinka suuri näiden tarve mahdollisesti on ja mitä näiden kurssien sisällössä tulisi erityisesti huomioida. Sähköinen kysely toteutettiin lastenlääkäri-, lastenneurologi- ja kehitysvammalääkäriyhdistysten avustuksella. Kyselyyn vastasi yhteensä 90 lääkäriä. Kyselyn tulokset osoittivat että vain harva erityistä tukea tarvitsevia lapsia hoitavista lääkäreistä tiesi Kelan järjestämistä omaishoitajakursseista, mutta lähes kaikki tunnistivat lapsiaan hoitaville vanhemmille kohdistettujen kuntoutuskurssien tarpeen. Lastaan hoitavien omaishoitajien kuormittuneisuus on tärkeä ottaa huomioon sosiaali- ja terveydenhuollon palveluja suunniteltaessa

Nature of Nitrogen Incorporation in BiVO4 Photoanodes through Chemical and Physical Methods

In recent years, BiVO4 has been optimized as a photoanode material to produce photocurrent densities close to its theoretical maximum under AM1.5 solar illumination. Its performance is, therefore, limited by its 2.4 eV bandgap. Herein, nitrogen is incorporated into BiVO4 to shift the valence band position to higher energies and thereby decreases the bandgap. Two different approaches are investigated: modification of the precursors for the spray pyrolysis recipe and post-deposition nitrogen ion implantation. Both methods result in a slight red shift of the BiVO4 bandgap and optical absorption onset. Although previous reports on N-modified BiVO4 assumed individual nitrogen atoms to substitute for oxygen, X-ray photoelectron spectroscopy on the samples reveals the presence of molecular nitrogen (i.e., N-2). Density functional theory calculations confirm the thermodynamic stability of the incorporation and reveal that N-2 coordinates to two vanadium atoms in a bridging configuration. Unfortunately, nitrogen incorporation also results in the formation of a localized state of approximate to 0.1 eV below the conduction band minimum of BiVO4, which suppresses the photoactivity at longer wavelengths. These findings provide important new insights on the nature of nitrogen incorporation into BiVO4 and illustrate the need to find alternative lower-bandgap absorber materials for photoelectrochemical energy conversion applications