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161.
162.
Anke Hagen Marie Lund Traulsen Wolff‐Ragnar Kiebach Bjoern Sejr Johansen 《Journal of synchrotron radiation》2012,19(3):400-407
Solid oxide fuel cells (SOFCs) are able to produce electricity and heat from hydrogen‐ or carbon‐containing fuels with high efficiencies and are considered important cornerstones for future sustainable energy systems. Performance, activation and degradation processes are crucial parameters to control before the technology can achieve breakthrough. They have been widely studied, predominately by electrochemical testing with subsequent micro‐structural analysis. In order to be able to develop better SOFCs, it is important to understand how the measured electrochemical performance depends on materials and structural properties, preferably at the atomic level. A characterization of these properties under operation is desired. As SOFCs operate at temperatures around 1073 K, this is a challenge. A spectroelectrochemical cell was designed that is able to study SOFCs at operating temperatures and in the presence of relevant gases. Simultaneous spectroscopic and electrochemical evaluation by using X‐ray absorption spectroscopy and electrochemical impedance spectroscopy is possible. 相似文献
163.
Duque JG Telg H Chen H Swan AK Shreve AP Tu X Zheng M Doorn SK 《Physical review letters》2012,108(11):117404
We exploit an energy level crossover effect [Haroz et al., Phys. Rev. B 77, 125405 (2008)] to probe quantum interference in the resonance Raman response from carbon nanotube samples highly enriched in the single semiconducting chiralities of (8,6), (9,4), and (10,5). UV Raman excitation profiles of G-band spectra reveal unambiguous signatures of interference between the third and fourth excitonic states (E(33) and E(44)). Both constructive and destructive responses are observed and lead to anomalous intensity ratios in the LO and TO modes. Especially large anomalies for the (10,5) structure result from nearly identical energies found for the two E(ii) transitions. The interference patterns demonstrate that the sign of the exciton-phonon coupling matrix elements changes for the LO mode between the two electronic states, and remains the same for the TO mode. Significant non-Condon contributions to the Raman response are also found. 相似文献
164.
Denysenko D Werner T Grzywa M Puls A Hagen V Eickerling G Jelic J Reuter K Volkmer D 《Chemical communications (Cambridge, England)》2012,48(9):1236-1238
Postsynthetic metal ion exchange in a benzotriazolate-based MFU-4l(arge) framework leads to a Co(II)-containing framework with open metal sites showing reversible gas-phase oxidation properties. 相似文献
165.
Dr. Chang‐Qi Ma Dr. Elena Mena‐Osteritz Dr. Markus Wunderlin Dr. Gisela Schulz Prof. Dr. Peter Bäuerle 《Chemistry (Weinheim an der Bergstrasse, Germany)》2012,18(40):12880-12901
The synthesis of generational dendritic oligothiophenes (DOTs) has been successfully achieved by a divergent/convergent approach that involves halogenation, boronation, and palladium‐catalyzed Suzuki coupling reactions. The key point in the presented synthetic approach is the use of trimethylsilyl (TMS) protecting groups, which allow for the core‐lithiation and subsequent boronation of the dendrons and for the peripheral ipso‐substitution with iodine monochloride or N‐bromosuccimide. In addition, the TMS protecting groups can be completely removed by using tetrabutylammonium fluoride, thus yielding only‐thiophene‐based dendrons and dendrimers. Due to their highly branched structure, all these synthesized DOTs are soluble in organic solvents. Chemical structures were confirmed by NMR spectroscopic, mass spectrometric, and elemental analysis. Concentration‐dependent 1H NMR spectroscopic investigations revealed that the higher generation compounds tend to aggregate in solution. Such an aggregation behavior was further confirmed by measuring with MALDI‐TOF MS. Both MALDI‐TOF MS and gel‐permeation chromatography (GPC) analyses confirmed the monodispersity of the DOTs. Furthermore, GPC results revealed that these DOT molecules adopt a condensed globular molecular shape. Their optical and electronic properties were also investigated. The results indicated that these DOTs comprise various conjugated α‐oligothiophenes with different chain lengths, which results in the higher generation compounds showing broad and featureless UV/Vis absorption spectra and ill‐defined redox waves. 相似文献
166.
María A. Ramírez Gisela M. Ortiz Alejandra Salerno Isabel A. Perillo María M. Blanco 《Tetrahedron letters》2012,53(11):1367-1369
In this work, we describe the synthesis of a series of 1,2,3-trisubstituted-1,4,5,6,7,8-hexahydro-1,3-diazocinium salts (1) by alkylation of the corresponding 1,2-diaryl-1,4,5,6,7,8-hexahydro-1,3-diazocines (2). Compounds 2 were obtained by ethyl polyphosphate-promoted cyclocondensation of N-aroyl-N′-arylpentamethylenediamines (3). Reaction of compounds 2 with alkyl iodides led to 1,2,3-trisubstituted 1,4,5,6,7,8-hexahydro-1,3-diazocinium iodides (1), a new family of cyclic amidinium salts. The best yields for the alkylation were achieved using a mixture of DCM–DMSO (10:1) as solvent. The reaction times of both, the cyclocondensation of compounds 3 and the reaction of 2 with alkyl halides, are dramatically decreased when using microwave irradiation. 相似文献
167.
Parolo ME Avena MJ Pettinari GR Baschini MT 《Journal of colloid and interface science》2012,368(1):420-426
The adsorption of tetracycline (TC) on montmorillonite was studied as a function of pH and Ca(2+) concentration using a batch technique complemented with X-ray diffraction and transmission electron microscopy. In the absence of Ca(2+), TC adsorption was high at low pH and decreased as the pH increased. In the presence of Ca(2+), at least two different adsorption processes took place in the studied systems, i.e., cation exchange and Ca-bridging. Cation exchange was the prevailing process at pH<5, and thus, TC adsorption decreased by increasing total Ca(2+) concentration. On the contrary, Ca-bridging was the prevailing process at pH>5, and thus, TC adsorption increased by increasing Ca(2+) concentration. The pH 5 represents an isoadsorption pH where both adsorption processes compensate each other. TC adsorption became independent of Ca(2+) concentration at this pH. For TC adsorption on Ca(2+)-montmorillonite in 0.01 M NaCl experiments, the ratio adsorbed TC/retained Ca(2+) was close to 1 in the pH range of 5-9, indicating an important participation of Ca(2+) in the binding of TC to montmorillonite. X-ray diffraction and transmission electron microscopy showed that TC adsorption induced intercalation between montmorillonite layers forming a multiphase system with stacking of layers with and without intercalated TC. 相似文献
168.
Quasi-isothermal curing of a polyester resin was studied at different catalyst concentrations and temperatures in-situ by 1H-NMR relaxometry and NIR spectroscopy simultaneously. Sample and probe temperatures were also recorded. An autocatalytic kinetic model, optionally including a diffusion term, was successfully applied to describe and predict the curing kinetics of the polyester resin as a function of temperature and catalyst concentration, although the diffusion effect is relatively weak in the investigated system under the experimental conditions. The corresponding kinetic coefficients and the reaction activation energy were obtained by fitting the models to the data, assuming an Arrhenius relation. 相似文献
169.
G. Kuri G. Materlik V. Hagen R. Wiesendanger 《Applied Physics A: Materials Science & Processing》2001,73(3):265-271
MgO (100) single crystals are implanted with 1.50-MeV Al+ and 3.00-MeV Al2
+ ions at a fluence of 1×1015 Al atoms cm-2 under high-vacuum conditions. The surface morphology of the substrate is measured in air using atomic force microscopy and
X-ray reflectometry followed by computer-simulated spectrum analysis. The ion-irradiated areas are found to protrude to different
heights on the nanometre scale. Small height differences are observed in the areas irradiated by Al+ and Al2
+ ions of comparable energy, dose rate and total fluence. The results indicate that protrusions are most likely caused by implantation-induced
point defects (vacancies) generated in the crystal during implantation. Other possibilities for the cause of protrusions are
discussed. Thermal treatment stimulates a partial recovery of the implantation damage and alters the topography of MgO surfaces.
Received: 22 May 2001 / Accepted: 30 May 2001 / Published online: 25 July 2001 相似文献
170.
A cascadic multigrid algorithm for semilinear elliptic problems 总被引:12,自引:0,他引:12
Gisela Timmermann 《Numerische Mathematik》2000,86(4):717-731
Summary. We propose a cascadic multigrid algorithm for a semilinear elliptic problem. The nonlinear equations arising from linear
finite element discretizations are solved by Newton's method. Given an approximate solution on the coarsest grid on each finer
grid we perform exactly one Newton step taking the approximate solution from the previous grid as initial guess. The Newton
systems are solved iteratively by an appropriate smoothing method. We prove that the algorithm yields an approximate solution
within the discretization error on the finest grid provided that the start approximation is sufficiently accurate and that
the initial grid size is sufficiently small. Moreover, we show that the method has multigrid complexity.
Received February 12, 1998 / Revised version received July 22, 1999 / Published online June 8, 2000 相似文献