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91.
M.M.A.J.?VonckenEmail author J.J.?Schermer G.J.?Bauhuis P.?Mulder P.K.?Larsen 《Applied Physics A: Materials Science & Processing》2004,79(7):1801-1807
The lateral etch rate of AlGaAs in HF in the Epitaxial Lift-Off (ELO) process consists of two parts, an intrinsic and a radius-induced part. The intrinsic part is studied with a new approach in which multiple release layers are introduced in one sample. By letting an essential ELO process parameter vary over the different release layers, this parameter is examined, using only samples from one wafer. In this study, the influence of thickness, aluminium fraction, and doping concentration of the release layer on the lateral etch rate is investigated. For release layers with thicknesses below 10 nm, a positive correlation between thickness and intrinsic etch rate is found. Thicker release layers do not result in higher etch rates. Increasing aluminium fractions in the AlxGa1-xAs release layers result in higher etch rates. For aluminium fractions between 0.3 and 1, this effect covers almost six orders of magnitude. From the width of the V-shaped etch slits in samples that have been etched for 12 hours or more, the selectivity, i.e., the ratio of the etch rate of AlxGa1-xAs to GaAs, is determined. Selectivities between 4.3 and 8.6×105 are found for x=0.3 and x=1, respectively. A variation in silicon doping is found to have no effect on the lateral etch rate, while increased zinc doping raises the etch rate significantly. PACS 81.05.Ea; 68.37.Hk; 81.15.Gh 相似文献
92.
Larsen J Rasmussen BS Hazell RG Skrydstrup T 《Chemical communications (Cambridge, England)》2004,(2):202-203
A disphosphine-palladium(0) complex capable of recognising barbiturates has been prepared. Oxidative addition studies with a barbitiurate:aryl iodide conjugate provided new Pd(ii) complexes where the positioning of the Pd-bound aryl group is controlled by the molecular recognition event. 相似文献
93.
Phipps RK Petersen BO Christensen KB Duus JØ Frisvad JC Larsen TO 《Organic letters》2004,6(20):3441-3443
[structure: see text] Hesseltin A 1, a novel compound of mixed polyketide-terpenoid origins was isolated from the filamentous fungus Penicillium hesseltinei. The structure and stereochemistry were determined from extensive one- and two-dimensional NMR and mass spectral data. 相似文献
94.
Optical waveguide sensor for on-line monitoring of bacteria 总被引:2,自引:0,他引:2
A grating-coupled planar optical waveguide sensor is presented for sensing of bacteria by evanescent waves. The waveguide design results in increased depth of penetration into the sample volume, which makes it suitable for detecting micrometer-sized biological objects. We tested the sensor's performance by monitoring the adhesion of Escherichia coli K12 cells to the sensor surface. 相似文献
95.
A coherent anti-Stokes Raman scattering microscope based on a Ti:sapphire femtosecond oscillator and a photonic crystal fiber is demonstrated. The nonlinear response of the fiber is used to generate the additional wavelength needed in the Raman process. The applicability of the setup is demonstrated by imaging of micrometer-sized polystyrene beads. 相似文献
96.
T.V. Andersen J. Thogersen S.R. Keiding J.J. Larsen 《Applied physics. B, Lasers and optics》2003,76(6):639-644
We demonstrate intracavity frequency doubling of a standard femtosecond Ti:sapphire oscillator. The cavity is extended with
a pair of focusing mirrors and a 0.5-mm-thick BBO crystal. We achieve a repetition rate of 50 MHz and simultaneously generate
22 mW of 55-fs pulses at 810 nm and 200 mW of 73-fs pulses at 405 nm, which corresponds to 4 nJ per pulse. We create a total
of 330-mW, 405-nm light when pumping the Ti:sapphire crystal with 5.7 W from an Ar-ion laser, corresponding to a conversion
efficiency of 5.7%. No saturation is found, which implies that higher outputs can be achieved with higher pump rates. Preliminary
results from the use of blue pulses as pump in an optical parametric amplifier seeded by pulses from a photonic crystal fiber
are presented.
Received: 27 January 2003 / Revised version: 27 March 2003 / Published online: 12 May 2003
RID="*"
ID="*"Corresponding author. Fax: +45-861/96199, E-mail: tva@chem.au.dk 相似文献
97.
Bearden IG Beavis D Besliu C Blyakhman Y Budick B Bøggild H Chasman C Christensen CH Christiansen P Cibor J Debbe R Enger E Gaardhøje JJ Germinario M Hagel K Hansen O Holm A Holme AK Ito H Jakobsen E Jipa A Jundt F Jørdre JI Jørgensen CE Karabowicz R Keutgen T Kim EJ Kozik T Larsen TM Lee JH Lee YK Løvhøiden G Majka Z Makeev A McBreen B Mikelsen M Murray M Natowitz J Nielsen BS Norris J Olchanski K Olness J Ouerdane D Płaneta R Rami F Ristea C Röhrich D Samset BH Sandberg D Sanders SJ 《Physical review letters》2003,90(10):102301
We present ratios of the numbers of charged antihadrons to hadrons (pions, kaons, and protons) in Au+Au collisions at sqrt[s(NN)]=200 GeV as a function of rapidity in the range y=0-3. While the ratios at midrapidity are approaching unity, the K(-)/K(+) and p;/p ratios decrease significantly at forward rapidities. An interpretation of the results within the statistical model indicates a reduction of the baryon chemical potential from mu(B) approximately 130 MeV at y=3 to mu(B) approximately 25 MeV at y=0. 相似文献
98.
An extensive library of 77Se chemical shifts have been generated from the NMR measurements on substituted (phenylseleno)benzenes, including 33 new compounds. The variation in chemical shifts cover 265 ppm ranging from 446 to 181 ppm. Crystal structures have been determined for nine selected representatives of the substituted (phenylseleno)-benzenes. The analysis of the crystal structures supported that through-space interactions between selenium and the ortho-substituent observed in the crystal structures also are likely to be present in solution. The variation in the 77Se NMR chemical shifts can be rationalised from the intramolecular interactions with the substituent in the ortho-position. Furthermore it appears that these ortho-effects are roughly additive, and that it is the actual interactions and not the resulting conformational constraints that are responsible for the variations in the 77Se NMR chemical shifts. 相似文献
99.
100.
We demonstrate, theoretically and experimentally, that an intense, elliptically polarized, nonresonant laser field can simultaneously force all three axes of a molecule to align along given axes fixed in space, thus inhibiting the free rotation in all three Euler angles. Theoretically, the effect is illustrated through time dependent quantum mechanical calculations. Experimentally, 3, 4-dibromothiophene molecules are aligned with a nanosecond laser pulse. The alignment is probed by 2D ion imaging of the fragments from a 20 fs laser pulse induced Coulomb explosion. 相似文献