162 research outputs found
Strain in epitaxial MnSi films on Si(111) in the thick film limit studied by polarization-dependent extended x-ray absorption fine structure
We report a study of the strain state of epitaxial MnSi films on Si(111)
substrates in the thick film limit (100-500~\AA) as a function of film
thickness using polarization-dependent extended x-ray absorption fine structure
(EXAFS). All films investigated are phase-pure and of high quality with a sharp
interface between MnSi and Si. The investigated MnSi films are in a thickness
regime where the magnetic transition temperature assumes a
thickness-independent enhanced value of 43~K as compared with that of
bulk MnSi, where . A detailed refinement of
the EXAFS data reveals that the Mn positions are unchanged, whereas the Si
positions vary along the out-of-plane [111]-direction, alternating in
orientation from unit cell to unit cell. Thus, for thick MnSi films, the unit
cell volume is essentially that of bulk MnSi --- except in the vicinity of the
interface with the Si substrate (thin film limit). In view of the enhanced
magnetic transition temperature we conclude that the mere presence of the
interface, and its specific characteristics, strongly affects the magnetic
properties of the entire MnSi film, even far from the interface. Our analysis
provides invaluable information about the local strain at the MnSi/Si(111)
interface. The presented methodology of polarization dependent EXAFS can also
be employed to investigate the local structure of other interesting interfaces.Comment: 11 pages, 10 figure
Insights into the Structure of Dot@Rod and Dot@Octapod CdSe@CdS Heterostructures
CdSe@CdS dot@rods with diameter around 6 nm and length of either
20, 27, or 30 nm and dot@octapods with pod diameters of ?15 nm and lengths of ?50
nm were investigated by X-ray absorption spectroscopy. These heterostructures are
prepared by seed-mediated routes, where the structure, composition, and morphology of
the CdSe nanocrystals used as a seed play key roles in directing the growth of the second
semiconducting domain. The local structural environment of all the elements in the
CdSe@CdS heterostructures was investigated at the Cd, S, and Se K-edges by taking
advantage of the selectivity of X-ray absorption spectroscopy, and was compared to pure
reference compounds. We found that the structural features of dot@rods are
independent of the size of the rods. These structures can be described as made of a
CdSe dot and a CdS rod, both in the wurtzite phase with a high crystallinity of both the
core and the rod. This result supports the effectiveness of high temperature colloidal
synthesis in promoting the formation of core@shell nanocrystals with very low
defectivity. On the other hand, data on the CdSe@CdS with octapod morphology suggest the occurrence of a core composed of
a CdSe cubic sphalerite phase with eight pods made of CdS wurtzite phase. Our findings are compared to current models
proposed for the design of functional heterostructures with controlled nanoarchitecture
Efficient Enzymatic Preparation of Flavor Esters in Water
A straightforward biocatalytic method for the enzymatic preparation of different flavor esters starting from primary alcohols (e.g., isoamyl, n-hexyl, geranyl, cinnamyl, 2-phenethyl, and benzyl alcohols) and naturally available ethyl esters (e.g., formate, acetate, propionate, and butyrate) was developed. The biotransformations are catalyzed by an acyltransferase from Mycobacterium smegmatis (MsAcT) and proceeded with excellent yields (80-97%) and short reaction times (30-120 min), even when high substrate concentrations (up to 0.5 M) were used. This enzymatic strategy represents an efficient alternative to the application of lipases in organic solvents and a significant improvement compared with already known methods in terms of reduced use of organic solvents, paving the way to sustainable and efficient preparation of natural flavoring agents
Nanostructures based on monoolein or diolein and amphiphilic gadolinium complexes as MRI contrast agents
Highly ordered two or three dimensional mesophases in aqueous solution could be usefully obtained by using monoolein (MO) or diolein (DO) monomers. Nanostructures (also indicated as nanoparticles, NPs)
of MO or DO containing different amounts (1%, 5%, 10% and 20%) of the synthetic amphiphilic gadolinium complex (C18)2DTPA(Gd) have been prepared and characterized for their relaxometric and
structural behaviors. The nanostructure is found in the 110–200 nm range for all investigated systems, while the presence of the gadolinium containing monomer produces a partial loss of the cubic
symmetry, as shown by Cryo-TEM images of NPs doped with 10% w/w of (C18)2DTPA(Gd). Gadolinium containing nanostructures display high relaxivity values (in the 10–15 mM1 s1 range at 25 and
20 MHz, with a further increase at 37°C for DO based NPs), and interesting relaxometric properties for their possible use as MRI contrast agents. NPs containing 10% w/w of (C18)2DTPA(Gd) (MO3-NPs and DO3-NPs) have been also derivatized by introducing 3% wt of (C18)2–Peg3000–FA to obtain targeted aggregates (MO3-NP–FA, DO3-NP–FA). A preferential uptake efficiency of DO3-NP–FA in IGROV-1 cells with respect to DO-NPs without folic acid is observed, specially when cells are incubated with low concentrations of nanostructures or at short incubation times, thus indicating its potential use as a target-selective delivery system for MRI contrast agents on tumor cells overexpressing the folate receptor
Supported metal nanoparticles with tailored catalytic properties through sol-immobilisation: applications for the hydrogenation of nitrophenols
The use of sol-immobilisation to prepare supported metal nanoparticles is an area of growing importance in heterogeneous catalysis; it affords greater control of nanoparticle properties compared to conventional catalytic routes e.g. impregnation. This work, and other recent studies, demonstrate how the properties of the resultant supported metal nanoparticles can be tailored by adjusting the conditions of colloidal synthesis i.e. temperature and solvent. We further demonstrate the applicability of these methods to the hydrogenation of nitrophenols using a series of tailored Pd/TiO2 catalysts, with low Pd loading of 0.2 wt%. Here, the temperature of colloidal synthesis is directly related to the mean particle diameter and the catalytic activity. Smaller Pd particles (2.2 nm, k = 0.632 min−1, TOF = 560 h−1) perform better than their larger counterparts (2.6 nm, k = 0.350 min−1, TOF = 370 h−1) for the hydrogenation of p-nitrophenol, with the catalyst containing smaller NPs found to have increased stability during recyclability studies, with high activity (>90% conversion after 5 minutes) maintained across 5 catalytic cycles
Hard X-ray microprobe highlights the structure of multi-quantum wells in electroabsorption-modulated lasers for optoelectronics
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