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1.
2.
Lithium Insertion Mechanism in Iron-Based Oxyfluorides with Anionic Vacancies Probed by PDF Analysis
Dr. Damien Dambournet Dr. Karena W Chapman Dr. Mathieu Duttine Dr. Olaf Borkiewicz Dr. Peter J Chupas Dr. Henri Groult 《ChemistryOpen》2015,4(4):443-447
The mechanism of lithium insertion that occurs in an iron oxyfluoride sample with a hexagonal–tungsten–bronze (HTB)-type structure was investigated by the pair distribution function. This study reveals that upon lithiation, the HTB framework collapses to yield disordered rutile and rock salt phases followed by a conversion reaction of the fluoride phase toward lithium fluoride and nanometer-sized metallic iron. The occurrence of anionic vacancies in the pristine framework was shown to strongly impact the electrochemical activity, that is, the reversible capacity scales with the content of anionic vacancies. Similar to FeOF-type electrodes, upon de-lithiation, a disordered rutile phase forms, showing that the anionic chemistry dictates the atomic arrangement of the re-oxidized phase. Finally, it was shown that the nanoscaling and structural rearrangement induced by the conversion reaction allow the in situ formation of new electrode materials with enhanced electrochemical properties. 相似文献
3.
Olaf Hansen 《Mathematical Methods in the Applied Sciences》2002,25(12):1075-1090
In this article we study the radiosity operator along an edge between two adjacent half‐planes. First we show that the radiosity operator is invertible in a whole scale of anisotropic Sobolev spaces. In the absence of any shadows we are able to derive regularity properties of the solution, which depend only on the angle between the half‐planes, the reflectivity coefficients and the right‐hand side. This work can be considered as a supplement to the article of Rathsfeld (Mathematical Methods in the Applied Sciences 1999; 22 : 217–241). Copyright © 2002 John Wiley & Sons, Ltd. 相似文献
4.
H. G. Bohlen W. von Oertzen R. Kalpakchieva B. Gebauer S. M. Grimes A. Lenz T. N. Massey M. Milin Ch. Schulz Tz. Kokalova S. Torilov S. Thummerer 《Physics of Atomic Nuclei》2003,66(8):1494-1500
The structure of neutron-rich beryllium isotopes has been investigated using different heavy-ion-induced transfer reactions. In neutron transfer reactions, the population of final states shows a strong sensitivity to the chosen core nucleus, i.e., the target nuclei 9Be or 10Be, respectively. Molecular rotational bands up to high excitation energies are observed with 9Be as the core due to its pronounced 2α-cluster structure, whereas only a few states at low excitation energies are populated with 10Be as the core. For 11Be, a detailed investigation has been performed for the three states at 3.41, 3.89, and 3.96 MeV, which resulted in the most probable spin-parity assignments 3/2+, 5/2?, and 3/2?, respectively. Furthermore, we have studied particle-hole states of 16C using the 13C(12C, 9C)16C reaction and found 14 previously unknown states. Using the 12C(12C, 9C)15C reaction, five new states were observed for 15C. 相似文献
5.
6.
A time discrete scheme is used to approximate the solution toa phase field system of PenroseFife type with a non-conservedorder parameter. An a posteriori error estimate is presentedthat allows the estimation of the difference between continuousand semidiscrete solutions by quantities that can be calculatedfrom the approximation and given data. 相似文献
7.
8.
We introduce a new technique for imaging oxygen concentrations in fuel/air mixtures that takes advantage of the different
responses of toluene and 3-pentanone to collisional quenching by molecular oxygen. Since laser-induced fluorescence signals
from both tracers upon excitation at 248 nm are spectrally well separated, simultaneous detection is possible. The technique
is first applied to instantaneous imaging in turbulent mixing processes of interacting seeded air and nitrogen flows.
Received: 1 August 2001 / Revised version: 29 October 2001 / Published online: 29 November 2001 相似文献
9.
Christoph Elschenbroich Jrn Plackmeyer Klaus Harms Olaf Burghaus Jürgen Pebler 《无机化学与普通化学杂志》2006,632(5):819-827
Trovacene Chemistry. 13 [1] On Being Lead and Mislead in the Synthesis of Di([5]trovacenyl)ketone Di([5]trovacenyl)ketone ( 3¨ ) has been prepared from lithio‐[5]trovacene and dimethylcarbamoyl chloride and studied by X‐ray diffraction, cyclic voltammetry, magnetic susceptometry and EPR spectroscopy. Slight variation of the synthetic protocol affords an unusual trinuclear complex 5 ? that is also fully characterized. Spin‐spin exchange interaction is smaller in 3¨ than in 1,1‐di([5]trovacenylethene ( 2¨ ), which differs from 3¨ by a replacement of O for CH2. The novel trinuclear complex 5 ? , however, displays exchange coupling very similar to that observed in 1‐methoxy‐2,5,6‐tri([5]trovacenyl)benzene ( 7 ? ). In both cases, an unsymmetrical triangular arrangement of S = 1/2 centers is encountered. These findings are discussed in terms of the nature of the respective spacers. 相似文献
10.
Summary The solubility parameters of cationic surfactants were obtained using the inverse gas chromatographic technique. The surfactants
didodecyl dimethyl ammonium bromide, dioctadecyl dimethyl ammonium bromide and dodecyl pyridinium chloride were used as stationary
phase and retention data of different probe solutes were measured at different temperatures. The results were analysed by
the combination of Flory-Huggins and Hildebrand theories, and the solubility parameters of the surfactants were obtained in
a range of temperatures between 80–120°C. 相似文献