Extended X-ray absorption fine structure

About: Extended X-ray absorption fine structure is a research topic. Over the lifetime, 10452 publications have been published within this topic receiving 276744 citations.

XANES, EXAFS and photocatalytic investigations on copper oxide nanoparticles and nanocomposites

Abstract: CuO nanoparticles (NPs) and Cu2O/CuO and CuO/TiO2 nanocomposites (NCs) have been synthesized by using a modified co-precipitation method with three different schemes of synthesis. The crystal structures and morphologies of the samples have been investigated using synchrotron X-ray diffraction and transmission electron microscopy, respectively. The detailed local electronic structures of the NPs and NCs have been determined using X-ray absorption near edge structure (XANES) and extended X-ray absorption fine structure (EXAFS) spectroscopy. O K-, Cu K- and Cu L-edge XANES spectra revealed a dominant +2 valence state of Cu in the case of the CuO NPs and CuO/TiO2 NCs, although Cu+1 was dominant in the Cu2O/CuO NCs. A comparison of the local atomic structure around the Cu sites revealed shorter Cu–O bond distances in the as-synthesized samples with respect to the bulk CuO or Cu2O. The Ti K-edge EXAFS fittings for the CuO/TiO2 NCs revealed that the local anatase TiO2 phase was formed, with a Ti–O bond distance of 1.98 A. We further demonstrated that the CuO NPs, and Cu2O/CuO and CuO/TiO2 NCs can serve as effective photocatalysts towards the degradation of two novel water pollutants, (i) methyl orange (MO) and (ii) potassium dichromate (PD), under visible light irradiation. It was found that the Cu2O/CuO NCs exhibit a higher photocatalytic activity towards the degradation of MO and PD than the CuO NPs or CuO/TiO2 NCs. The mechanism of the photodegradation of MO and PD is also discussed in terms of possible chemical reactions, along with the electronic structure and surface properties of the samples.

Characterization of the particulate methane monooxygenase metal centers in multiple redox states by X-ray absorption spectroscopy.

Abstract: The integral membrane enzyme particulate methane monooxygenase (pMMO) converts methane, the most inert hydrocarbon, to methanol under ambient conditions. The 2.8-A resolution pMMO crystal structure revealed three metal sites: a mononuclear copper center, a dinuclear copper center, and a nonphysiological mononuclear zinc center. Although not found in the crystal structure, solution samples of pMMO also contain iron. We have used X-ray absorption spectroscopy to analyze the oxidation states and coordination environments of the pMMO metal centers in as-isolated (pMMO(iso)), chemically reduced (pMMO(red)), and chemically oxidized (pMMO(ox)) samples. X-ray absorption near-edge spectra (XANES) indicate that pMMO(iso) contains both Cu(I) and Cu(II) and that the pMMO Cu centers can undergo redox chemistry. Extended X-ray absorption fine structure (EXAFS) analysis reveals a Cu-Cu interaction in all redox forms of the enzyme. The Cu-Cu distance increases from 2.51 to 2.65 A upon reduction, concomitant with an increase in the average Cu-O/N bond lengths. Appropriate Cu2 model complexes were used to refine and validate the EXAFS fitting protocols for pMMO(iso). Analysis of Fe EXAFS data combined with electron paramagnetic resonance (EPR) spectra indicates that Fe, present as Fe(III), is consistent with heme impurities. These findings are complementary to the crystallographic data and provide new insight into the oxidation states and possible electronic structures of the pMMO Cu ions.

X-ray K-edge absorption spectra of Fe minerals and model compounds: II. EXAFS

Abstract: K-edge extended X-ray absorption fine structure (EXAFS) spectra of Fe in varying environments in a suite of well-characterized silicate and oxide minerals were collected using synchrotron radiation and analyzed using single scattering approximation theory to yield nearest neighbor Fe-O distances and coordination numbers. The partial inverse character of synthetic hercynite spinal was verified in this way. Comparison of the results from all samples with structural data from X-ray diffraction crystal structure refinements indicates that EXAFS-derived first neighbor distances are generally accurate to ±0.02 A using only theoretically generated phase information, and may be improved over this if similar model compounds are used to determine EXAFS phase functions. Coordination numbers are accurate to ±20 percent and can be similarly improved using model compound EXAFS amplitude information. However, in particular cases the EXAFS-derived distances may be shortened, and the coordination number reduced, by the effects of static and thermal disorder or by partial overlap of the longer Fe-O first neighbor distances with second neighbor distances in the EXAFS structure function. In the former case the total information available in the EXAFS is limited by the disorder, while in the latter case more accurate results can in principle be obtained by multiple neighbor EXAFS analysis. The EXAFS and XANES spectra of Fe in Nain, Labrador osumulite and Lakeview, Oregon plagioclase are also analyzed as an example of the application of X-ray absorption spectroscopy to metal ion site occupation determination in minerals.