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Stefan Filipp Yuji Hasegawa Rudolf Loidl Helmut Rauch 《Journal of research of the National Institute of Standards and Technology》2005,110(3):251-257
We present a split-beam neutron interferometric experiment to test the non-cyclic geometric phase tied to the spatial evolution of the system: the subjacent two-dimensional Hilbert space is spanned by the two possible paths in the interferometer and the evolution of the state is controlled by phase shifters and absorbers. A related experiment was reported previously by some of the authors to verify the cyclic spatial geometric phase. The interpretation of this experiment, namely to ascribe a geometric phase to this particular state evolution, has met severe criticism. The extension to non-cyclic evolution manifests the correctness of the interpretation of the previous experiment by means of an explicit calculation of the non-cyclic geometric phase in terms of paths on the Bloch-sphere. The theoretical treatment comprises the cyclic geometric phase as a special case, which is confirmed by experiment. 相似文献
996.
基于蒸汽炉物煅烧氧化铋构成复合物自由引导压电材料性能的研究 总被引:1,自引:0,他引:1
YujiEnomoto KazumiKato HiroshiMatsuda 《苏州大学学报(工科版)》2004,24(5):6-7
由于环境污染问题,取代传统的基于引导的PZT自由引导压电材料得到了发展。其中CaBi4Ti4O15由于其多极性显示出铁和压电特性。在早期研究中,Ca-Bi-Ti合成醇盐的旋转涂层薄膜作为一个前期方案,通过钙、铋的氧化物和锑的异丙氧化物在酒精和2-甲氧基乙氧基混合物中的化学反应已经很好地合 相似文献
997.
Bames Karl Sauer E. Dinslage J. Großfeld Griebel Kluge Willy Lindner W. Schreiber Kanitz Schwaibold Schloemer Nelly Neuenschwander-Lemmer Lars Erlandsen W. Ludorff Pawletta Beckel Diemair Jesser Schormüller Lindner R. Strohecker G. Steinhoff Steinbeck Mohler W. Wodsak Weinig Reichard Brüning R. Grau Hans Hawelka O. Windhausen Bäurle H. Schubert K. Müller Hanak und K. Höll 《Zeitschrift für Lebensmitteluntersuchung und -Forschung A》1942,84(1):45-96
Ohne Zusammenfassung 相似文献
998.
The adsorption and reaction of toluene on vanadyl pyrophosphate catalysts was studied by in situ infrared spectroscopy. Strongly
adsorbed benzaldehyde and physically adsorbed cyclic anhydride species were observed at temperatures above 523 K. Water formed
during reaction generates acid hydroxyl groups which cause a stronger adsorption of benzaldehyde and consecutive oxidation
reactions. By co-adsorption of pyridine the acid sites are blocked and the deeper oxidation is suppressed.
This revised version was published online in August 2006 with corrections to the Cover Date. 相似文献
999.
The main concern of the present publication is the computation of dynamic loads of wind turbine power trains, with particular emphasis on planetary gearbox loads. The applied mathematical approach relies on a non‐linear finite element method, which is extended by multi‐body system functionalities, and aerodynamics based on the blade element momentum theory. Copyright © 2007 John Wiley & Sons, Ltd. 相似文献
1000.
Ulf Stalmach Heiner Detert Herbert Meier Volker Gebhardt Dietrich Haarer Andreas Bacher Hans-Werner Schmidt 《Optical Materials》1998,9(1-4):77-81
The preparation of LEDs with poly( p-phenylenevinylene) (PPV) as emitting material is well established. However, due to the presence of a distribution of conjugated chain lengths in the polymer, systematic investigations of the electroluminescence with polymeric materials are difficult, as far as the optical emission is concerned. We are studying the relationship between structural variation of substituted oligo(p-phenylenevinylene)s and their electroluminescent behaviour using a series of distyrylbenzenes with a variety of substituents in order to investigate their influence on the electroluminescence (EL). Furthermore, we synthesized a homologous series of monodisperse oligo(2,5-dipropoxy-1,4-phenylenevinylene)s with up to 11 repeating units. This series covers the spectrum from monomer to polymer. The influence on the EL can be investigated by preparing single layer LEDs using vapor deposition or spincoating of the oligomers in a polystyrene (PS) matrix. The comparison of photoluminescence (PL)- and EL-spectra shows that the photophysical properties of the oligomers are strongly altered by aggregation phenomena. 相似文献