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61.
Instability of the melt flow in VGF growth with a traveling magnetic field   总被引:1,自引:0,他引:1  
The linear instability of a thermally stratified melt flow in the VGF configuration driven by a traveling magnetic field (TMF) is considered numerically and experimentally. The dependency of the instability threshold on the governing parameters is found for several cuts through the parameter space covering a wide range of possible applications. In a first approximation the linear instability occurs when the dimensionless TMF forcing parameter reaches the magnitude of the Grashof number. This is particularly true in a medium-sized crucible where the first instability is axisymmetric and sub-critical. As the Grashof number increases the flow develops self-similar boundary layers and the instability becomes three-dimensional. The instability originates in the bottom boundary layer where the convection tends to suppress the imposed temperature gradient in the central part of the melt zone. It is shown that the TMF may serve as a tool to control the phase interface shape without causing flow instationarity when the crucible diameter exceeds a certain value. This value is estimated to be around 6 cm for GaAs. The flow stays stable if the TMF is used for a reversal of the meridional flow with the aim to remove a possible dopant concentration peak on the axis.  相似文献   
62.
    
In our two-paper series, we first present the development of ReaxFF CHOCl parameters using the recently published ParAMS parametrization tool. In this second part, we update the reactive Molecular Dynamics – Quantum Mechanics coupling scheme ChemTraYzer and combine it with our new ReaxFF parameters from Part I to study formation and decomposition processes of chlorinated dibenzofurans. We introduce a self-learning method for recovering failed transition-state searches that improves the overall ChemTraYzer transition-state search success rate by 10 percentage points to a total of 48 %. With ChemTraYzer, we automatically find and quantify more than 500 reactions using transition state theory and DFT. Among the discovered chlorinated dibenzofuran reactions are numerous reactions that are new to the literature. In three case studies, we discuss the set of reactions that are most relevant to the dibenzofuran literature: (i) bimolecular reactions of the chlorinated-dibenzofuran precursors phenoxy radical and 1,3,5-trichlorobenzene, (ii) dibenzofuran chlorination and pyrolysis, and (iii) oxidation of chlorinated dibenzofurans.  相似文献   
63.
    
Heterogeneous catalytic ammoxidation provides an eco-friendly route for the cyanide-free synthesis of nitrile compounds, which are important precursors for synthetic chemistry and pharmaceutical applications. However, in general such a process requires high pressures of molecular oxygen at elevated temperatures to accelerate the oxygen reduction and imine dehydrogenation steps, which is highly risky in practical applications. Here, we report an electric field enhanced ammoxidation system using a supported Fe clusters catalyst (Fe/NC), which enables efficient synthesis of nitriles from the corresponding aldehydes under ambient air pressure at room temperature (RT). A synergistic effect between the external electric field and the Fe/NC catalyst promotes the ammonia activation and the dehydrogenation of the generated imine intermediates and avoids the unwanted backwards reaction to aldehydes. This electric field enhanced ammoxidation system presents high efficiency and selectivity for the conversion of a series of aldehydes under mild conditions with high durability, rendering it an attractive process for the green synthesis of nitriles with fragile functional groups.  相似文献   
64.
Constructing a reliable solid-electrolyte interphase (SEI) is imperative for enabling highly reversible zinc metal (Zn0) electrodes. Contrary to conventional “bulk solvation” mechanism, we found the SEI structure is dominated by electric double layer (EDL) adsorption. We manipulate the EDL adsorption and Zn2+ solvation with ether additives (i.e. 15-crown-5, 12-crown-4, and triglyme). The 12-crown-4 with medium adsorption on EDL leads to a layer-structured SEI with inner inorganic ZnFx/ZnSx and outer organic C−O−C components. This structure endows SEI with high rigidness and strong toughness enabling the 100 cm2 Zn||Zn pouch cell to exhibit a cumulative capacity of 4250 mAh cm−2 at areal-capacity of 10 mAh cm−2. More importantly, a 2.3 Ah Zn||Zn0.25V2O5n H2O pouch cell delivers a recorded energy density of 104 Wh Lcell−1 and runs for >70 days under the harsh conditions of low negative/positive electrode ratio (2.2 : 1), lean electrolyte (8 g Ah−1), and high-areal-capacity (≈13 mAh cm−2).  相似文献   
65.
    
Aqueous rechargeable zinc-ion batteries (ARZBs) are impeded by the mutual problems of unstable cathode, electrolyte parasitic reactions, and dendritic growth of zinc (Zn) anode. Herein, a triple-functional strategy by introducing the tetramethylene sulfone (TMS) to form a hydrated eutectic electrolyte is reported to ameliorate these issues. The activity of H2O is inhibited by reconstructing hydrogen bonds due to the strong interaction between TMS and H2O. Meanwhile, the preferentially adsorbed TMS on the Zn surface increases the thickness of double electric layer (EDL) structure, which provides a shielding buffer layer to suppress dendrite growth. Interestingly, TMS modulates the primary solvation shell of Zn2+ ultimately to achieve a novel solvent co-intercalation ((Zn-TMS)2+) mechanism, and the intercalated TMS works as a “pillar” that provides more zincophilic sites and stabilizes the structure of cathode (NH4V4O10, (NVO)). Consequently, the Zn||NVO battery exhibits a remarkably high specific capacity of 515.6 mAh g−1 at a low current density of 0.2 A g−1 for over 40 days. This multi-functional electrolytes and solvent co-intercalation mechanism will significantly propel the practical development of aqueous batteries.  相似文献   
66.
A high voltage electric pulse can be applied to induce the uptake of DNA into cells and the release of protein from cells. In transformation procedures, electroporation is widely used since the technique is simple, rapid, reproducible, and highly efficient. In extraction of protein, on the other hand, electroextraction has many advantages over other conventional extractions. We have developed a highly efficient method for the electroporation of fission yeast. In particular, application of a high voltage electric pulse to fission yeast improves the cellular uptake and release of macromolecules controlled by both osmotic conditions and electric field strength.
Minoru SugaEmail:
  相似文献   
67.
An experimental study was conducted to investigate the effects of several operational parameters in the emission spectra, in the 400-850 nm wavelength region, of a laboratory Argon plasma source. In particular, the emission spectra of the inductively coupled plasma and the Helicon plasma modes of operation were compared. Comparisons of spectra point to a significant increase in the ionization fraction of the plasma for the Helicon mode of operation. The spectral measurements allow one to determine the major trends in the plasma electron density for various parameters such as power delivered to the helical antenna, propellant mass flow rate, and applied external magnetic field intensity.Analysis of a prominent Argon single ion line, at 434.8 nm, points out that the plasma electron density increases linearly with the power delivered to the helical antenna, and that there is an optimum propellant mass flow rate for maximum ionization fraction. Additional analysis of the same line shows that above a minimum applied axial magnetic field intensity, the variation in the magnetic field strength has little effect on the plasma electron density.  相似文献   
68.
69.
交流阻抗法作为一种新型的无标记、全程动态、实时分析方法已在细胞研究中得到了广泛应用。本文综述了基于交流阻抗法进行细胞分析的研究新进展,重点对非法拉第阻抗谱法和法拉第阻抗谱法用于细胞分析的原理及应用进行了总结,主要包括交流阻抗法在细胞形态、细胞生长、细胞增殖、细胞凋亡以及作用于细胞的药效和毒性研究中的应用,并对其发展趋势进行了展望。  相似文献   
70.
我们利用具有不同对称性的同分异构体,通过改变分子间氢键网络,操控单链磁体行为,成功合成了2例化合物:[Ni(L1)][Fe(Tp)(CN)3]2·3.5H2O (1)和[Ni(L2)][Fe(Tp)(CN)3]2·3H2O (2),其中Tp=hydrotris (pyrazolyl) borate,L1=3,4-bis (1H-imid-azol-1-yl) thiophen,L2=1,2-bis (1H-imidazol-1-yl) thiophen)。磁性研究表明,12表现为具有不同矫顽场的单链磁体行为。1的矫顽场为8.41 kOe,而2的矫顽场为3.84 kOe。  相似文献   
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