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排序方式: 共有573条查询结果,搜索用时 15 毫秒
1.
E. S. Moskalenko M. Larsson K. F. Karlsson P. O. Holtz B. Monemar W. V. Schoenfeld P. M. Petroff 《Physics of the Solid State》2007,49(10):1995-1998
We report on low-temperature microphotoluminescence (μ-PL) measurements of InAs/GaAs quantum dots (QDs) exposed to a lateral
external electric field. It is demonstrated that the QDs’ PL signal could be increased severalfold by altering the external
and/or the internal electric field, which could be changed by an additional infrared laser. A model which accounts for a substantially
faster lateral transport of the photoexcited carriers achieved in an external electric field is employed to explain the observed
effects. The results obtained suggest that the lateral electric fields play a major role for the dot luminescence intensity
measured in our experiment—a finding which could be used to tailor the properties of QD-based optoelectronic applications.
The text was submitted by the authors in English. 相似文献
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4.
The gas phase reaction between CO2 and lanthanide atoms. A test of a model for the isokinetic effect
Summary Co3O4, NiCo2O4 and LaCo2O4catalysts were synthesizedby the citric acid-ligated method. These catalysts containing Co-oxide active components can largely
lower the temperature of soot combustion under tight contact conditions. Under the conditions of loose contact NiCo2O4 cannot promote soot combustion, but LaCo2O4 can effectively promote soot combustion because the nanometric perovskite-type catalyst LaCoO3produced in the LaCo2O4sample.</o:p> 相似文献
5.
Torabi F Ramanathan K Larsson PO Gorton L Svanberg K Okamoto Y Danielsson B Khayyami M 《Talanta》1999,50(4):787-797
An electrochemical method for the measurement of NAD(+) and NADH in normal and cancer tissues using flow injection analysis (FIA) is reported. Reticulated vitreous carbon (RVC) electrodes with entrapped l-lactate dehydrogenase (LDH) and a new redox polymer containing covalently bound toluidine blue O (TBO) were employed for this purpose. Both NAD(+) and NADH were estimated coulometrically based on their reaction with LDH. The latter was immobilized on controlled pore glass (CPG) by cross-linking with glutaraldehyde and packed within the RVC. The concentrations of NAD(+) and NADH in the tissues, estimated using different electron mediators such as ferricyanide (FCN), meldola blue (MB) and TBO have also been compared. The effects of flow rate, pH, applied potential (versus Ag/AgCl reference) and adsorption of the mediators have also been investigated. Based on the measurements of NAD(+) and NADH in normal and cancer tissues it has been concluded that the NADH concentration is lower, while the NAD(+) concentration is higher in cancer tissues. Amongst the electron mediators TBO was found to be a more stable mediator for such measurements. 相似文献
6.
Philip Wormald Kristina Wickholm Per Tomas Larsson Tommy Iversen 《Cellulose (London, England)》1996,3(1):141-152
An investigation into the effects of mechanical treatment and hydration on the order of cellulose substrates (microcrystalline cellulose and Cladophora cellulose) was performed by the use of ball milling followed by cyclic wetting and drying. The results, monitored by13C-CP/MAS NMR-spectroscopy, were evaluated by calculation of the crystallinity indices and principal component analysis of the NMR data acquired. The results showed that a large part of the disorder induced by the mechanical treatment of cellulose by ball milling is reversible and reordering upon hydration leads to the cellulose I form initially present. The C4 signals corresponding to the reversibly disordered cellulose chains are observed in the amorphous region between 79 and 86 ppm in the13C-CP/MAS NMR-spectra together with signals from cellulose chains on the surface of ordered regions. The peak cluster which contains the C2, C3 and C5 ring carbons can be divided into two specific spectral regions; one between 74 and 77 ppm largely originates from ring carbons within disordered cellulose structures, and one between 70 and 74 ppm contains larger contributions from ordered cellulose. The behaviour of the celluloses upon milling is in accordance with a concept of ordered cellulose fibrils containing amorphous cellulose mainly as surface layers and induced reversible lattice distortions. 相似文献
7.
Dissociative recombination of the weakly bound NO-dimer cation: cross sections and three-body dynamics 总被引:1,自引:0,他引:1
Petrignani A Andersson PU Pettersson JB Thomas RD Hellberg F Ehlerding A Larsson M van der Zande WJ 《The Journal of chemical physics》2005,123(19):194306
Dissociative recombination (DR) of the dimer ion (NO)(2) (+) has been studied at the heavy-ion storage ring CRYRING at the Manne Siegbahn Laboratory, Stockholm. The experiments were aimed at determining details on the strongly enhanced thermal rate coefficient for the dimer, interpreting the dissociation dynamics of the dimer ion, and studying the degree of similarity to the behavior in the monomer. The DR rate reveals that the very large efficiency of the dimer rate with respect to the monomer is limited to electron energies below 0.2 eV. The fragmentation products reveal that the breakup into the three-body channel NO+O+N dominates with a probability of 0.69+/-0.02. The second most important channel yields NO+NO fragments with a probability of 0.23+/-0.03. Furthermore, the dominant three-body breakup yields electronic and vibrational ground-state products, NO(upsilon=0)+N((4)S)+O((3)P), in about 45% of the cases. The internal product-state distribution of the NO fragment shows a similarity with the product-state distribution as predicted by the Franck-Condon overlap between a NO moiety of the dimer ion and a free NO. The dissociation dynamics seem to be independent of the NO internal energy. Finally, the dissociation dynamics reveal a correlation between the kinetic energy of the NO fragment and the degree of conservation of linear momentum between the O and N product atoms. The observations support a mechanism in which the recoil takes place along one of the NO bonds in the dimer. 相似文献
8.
Körner A Larsson A Piculell L Wittgren B 《The journal of physical chemistry. B》2005,109(23):11530-11537
A systematic study of the dissolution of dry, polydisperse poly(ethylene oxide) (PEO) samples, obtained from mixtures of low-molecular-weight and high-molecular-weight PEO, was made. During the dissolution process, the individual release of the low- and high-molecular-weight fractions was monitored. The high-molecular-weight/low-molecular-weight ratio controls the release rate, and the fraction of high-molecular-weight polymers dominates the effect on the overall release rate in mixed PEO tablets. Both fractions are released at the same rate during the main part of the dissolution process; however, during the initial dissolution period a fractionation occurs. The release rate is not a unique function of the average molecular weight of the polymer, but also depends on the polydispersity. By contrast, the average dimension of a polymer coil, as given by the intrinsic viscosity, gives a good prediction of the release rate irrespective of the polydispersity or details of the molecular weight distribution. 相似文献
9.
The natural radiative lifetime of the 3s4p
1
P
1 level of neutral magnesium was measured by pulsed level-crossing spectroscopy at the short excitation wavelength of 202.6 nm. We obtained =13.4(5) ns for this state, strongly deviating from a previous beam-foil result, but in good agreement with a multi-configuration Hartree-Fock calculation. A discussion of the applicability of the pulsed Hanle effect method is given. 相似文献
10.
A number of 1-allylthio and 1-crotylthio 1-aminoalkenes derived from ketones and active methylene compounds has been prepared and rearranged to the corresponding thioamides (thio-Claisen rearrangement). Besides rearrangement products, small amounts of 1-alkyl-thio-N-alkyl-N-phenyl-1-aminoalkenes have also been isolated. When the ketene derivatives did possess a H-atom on nitrogen, cleavage of the formed thioamide produced phenyl isothiocyanate and substituted active methylene compounds. 相似文献