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Träfflista för sökning "WFRF:(Chen Wei) srt2:(2000-2004)"

Sökning: WFRF:(Chen Wei) > (2000-2004)

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1.
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2.
  • Cao, Han, et al. (författare)
  • Fabrication of 10 nm enclosed nanofluidic channels
  • 2002
  • Ingår i: Applied Physics Letters. - : AIP Publishing. - 0003-6951 .- 1077-3118. ; 81:1, s. 174-176
  • Tidskriftsartikel (refereegranskat)abstract
    • We made uniform arrays of nanometer scale structures using nanoimprint lithography over large areas (100 mm wafers). The nanofluidic channels were further narrowed and sealed by techniques that are based on nonuniform deposition. The resulting sealed channels have a cross section as small as 10 nm by 50 nm, of great importance for confining biological molecules into ultrasmall spaces. These techniques can be valuable fabrication tools for Nanoelectromechanical Systems and Micro/Nano Total Analysis Systems.
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3.
  • Chen, Li Choo, et al. (författare)
  • Performance and Load Issues in TINA Networks
  • 2002
  • Ingår i: Proceedings for TINA Workshop 2002 Telecommunications Technology for the Next Decade. ; , s. 29-32
  • Konferensbidrag (refereegranskat)
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4.
  • Chen, Wei, et al. (författare)
  • Crystal field, phonon coupling and emission shift of Mn2+ in ZnS:Mn nanoparticles
  • 2001
  • Ingår i: Journal of Applied Physics. - : AIP Publishing. - 0021-8979 .- 1089-7550. ; 89, s. 1120-1129
  • Tidskriftsartikel (refereegranskat)abstract
    • The Mn2+ emission wavelengths are at 591, 588, 581 and 570 nm, respectively, for the similar to 10, similar to4.5, similar to3.5 nm sized nanoparticles and the ZnS:Mn nanoparticles formed in an ultrastable zeolite-Y. To reveal the cause for the shift, the crystal field and phonon coupling were investigated. The results show that the predominant factor for the shift is the phonon coupling, whose strength is size dependent and is determined by both the size confinement and the surface modification of the nanoparticles. Although the crystal field strength decreases with the decreasing of the particle size, its change has little contribution to the emission shift of Mn2+ in ZnS:Mn nanoparticles. (C) 2001 American Institute of Physics.
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5.
  • Chen, Wei, et al. (författare)
  • Energy structure and fluorescence of Eu2+ in ZnS:Eu nanoparticles
  • 2000
  • Ingår i: Physical Review B. - 1098-0121. ; 61:16, s. 11021-11024
  • Tidskriftsartikel (refereegranskat)abstract
    • Eu2+-doped ZnS nanoparticles with an average size of around 3 nm were prepared, and an emission band around 530 nm was observed. By heating in air at 150 degrees C, this emission decreased, while the typical sharp line emission of Eu3+ increased. This suggests that the emission around 530 nm is from intraion transition of Eu2+: In bulk ZnS:Eu2+, no intraion transition of Eu2+ was observed because the excited states of Eu2+ are degenerate with the continuum of the ZnS conduction band. We show that the band gap in ZnS:Eu2+ nanoparticles opens up due to quantum confinement, such that the conduction band of ZnS is higher than the first excited state of Eu2+, thus enabling the intraion transition of Eu2+ to occur.
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6.
  • Chen, Weimin, 1959-, et al. (författare)
  • Nature and Formation of Non-Radiative Defects in GaNAs and InGaAsN
  • 2002
  • Ingår i: MRS Fall Meeting 2001,2001. - Materials Research Society Symposium - Proceedings, Vol. 692 : MRS. ; , s. 67-72
  • Konferensbidrag (refereegranskat)abstract
    •  The optically detected magnetic resonance (ODMR) technique has been employed to examine the nature and formation mechanism of non-radiative defects in GaNAs and InGaAsN. In both alloys, two defects were observed and were shown to be deep-level, non-radiative recombination centers. One of the defects has been identified as a complex involving an AsGa antisite. These two defects gain more importance with increasing N composition up to 3%, presumably due to an increase in their concentration. With a further higher N composition, the defects start to lose importance in carrier recombination that is attributed to an increasingly important role of other new non-radiative channels introduced with a high N composition. On the other hand, effect of In composition up to 3% seems to be only marginal. Both defects were shown to be preferably introduced in the alloys during low-temperature growth by molecular beam epitaxy (MBE), but can be rather efficiently removed by post-growth rapid thermal annealing.
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7.
  • Ji, Xiaoyan, et al. (författare)
  • Determination of dissolution kinetics of K2SO4 crystal with ion selective electrode
  • 2001
  • Ingår i: Chemical Engineering Science. - 0009-2509 .- 1873-4405. ; 56, s. 7017-7024
  • Tidskriftsartikel (refereegranskat)abstract
    • The dissolution kinetics of potassium sulfate crystals was studied and the effects of hydrodynamic situation and temperature on the dissolution were investigated. The dissolution was determined by measuring the change of electromotive force (E) with the potassium ion selective electrode. From the values of E, the concentration of K+ was calculated combined with an activity coefficient model. The results are accurate and rapid, the maximum deviation is less than 2%. Theory, developed for constant bulk concentration in a rotating disk system, was modified in order to analyze the general grain dissolution process. Normal distribution was introduced in calculating the area of crystals in order to obtain reliable dissolution rate. Using the modified theory diffusion rate constant, equilibrium exchange rate constant and thickness of diffusion layer were obtained. It is found that the diffusion rate constants increase while the thickness of diffusion layer decreases with the increase of temperature and stirring speed; the equilibrium exchange rate is dependent on bulk concentration.
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9.
  • Liu, C, et al. (författare)
  • The study of dissolution kinetics of K2SO4 crystal in aqueous ethanol solutions with a statistical rate theory
  • 2004
  • Ingår i: Chinese Journal of Chemical Engineering. - 1004-9541 .- 2210-321X. ; 12, s. 128-130
  • Tidskriftsartikel (refereegranskat)abstract
    • Dissolution kinetics of K2SO4 crystal in aqueous ethanol solutions was studied on-line with ion selective electrode. The concentration of K2SO4 was calculated from the determined electromotive force in which the activity coefficient of components in the liquid phase was calculated with the Pitzer equation. Dissolution kinetic parameters in the modified statistical rate theory were regressed. The correlation results show that dissolution rate of K2SO4 is slower in aqueous ethanol solutions than that in aqueous solutions. The two most important reasons are as follows: (1) The solubility Of K2SO4 in aqueous ethanol solutions is lower than that in aqueous solutions, which causes a decrease of the driving force of mass transfer. (2) The process of surface reaction Of K2SO4 became slower due to the addition of ethanol, so that the whole process is mainly dominated by the surface reaction instead of mass transfer.
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