Coherent polarization stabilization in large-aperture rectangular post bottom-emitting vertical-cavity surface-emitting lasers

The output characteristics of large-aperture rectangular post bottom-emitting vertical-cavity surface-emitting lasers (VCSELs) were investigated. It was shown that the output power of the rectangle VCSELs can be up to 660 mW at a current of 5 A. Both H-polarization (horizontal) and V-polarization (vertical) demonstrated a coherent stabilization over the entire range of operation current, and coherent spectrum blue-shift of H-polarization light occurred with respect to V-polarization light at three different injected currents. The polarization states of output light were stabilized in the two orthogonal directions and H-polarization was the most principal polarization which was parallel to the longer side of the rectangular aperture. From the relationship between polarization ratio and aspect ratio of the oxidation confinement aperture (OCA), it was found that the highest polarization ratio (about 2:1) took place when the appropriate aspect ratio was 5:3, which meant better polarization stabilization in large-aperture VCSELs.     

Heat-Resistant Polymer-Grafted Carbon Black: Grafting of Poly(Amide-Imide) Onto Carbon Black

Aromatic poly(amide-imide) with terminal isocyanate groups (PAINCO) was prepared by the polycondensation of trimellitic anhydride and a slight excess of 4,4′-diphenylmethane diisocyanate in N-methyl-2-pyrrolidone (NMP) at 160°C for 20 h. PAI was effectively grafted onto the surface by the reaction of PAI-NCO with carbon black: the percentage of grafting onto FW 200 and Neospectra II was determined to be 41.2 and 39.5%, respectively. When the carboxyl and phenolic hydroxyl groups on carbon black were blocked by treatment with diazomethane, the grafting of PAI-NCO onto the treated carbon black does not proceed. Therefore, it is concluded that PAI-NCO reacts with the carboxyl and phenolic hydroxyl groups on carbon black and PAI is grafted through amide and urethane bonds, respectively. The reaction of PAI-NCO with carbon black was accelerated by the addition of amines as catalyst and by raising of the reaction temperature. Thermogravimetric analysis indicated that PAI-grafted carbon black was stable in air up to about 300°C. The PAI-grafted carbon black was found to give a stable colloidal dispersion in NMP.     

Comparison between N_2 and O_2 anneals on the integrity of an Al_2O_3/Si_3N_4/SiO_2/Si memory gate stack

In this paper the endurance characteristics and trap generation are investigated to study the effects of different postdeposition anneals(PDAs) on the integrity of an Al2O3/Si3N4/SiO2/Si memory gate stack. The flat-band voltage(Vfb)turnarounds are observed in both the programmed and erased states of the N2-PDA device. In contrast, this turnaround is observed only in the erased state of the O2-PDA device. The Vfbin the programmed state of the O2-PDA device keeps increasing with increasing program/erase(P/E) cycles. Through the analyses of endurance characteristics and the low voltage round-trip current transients, it is concluded that in both kinds of device there are an unknown type of pre-existing characteristic deep traps and P/E stress-induced positive oxide charges. In the O2-PDA device two extra types of trap are also found: the pre-existing border traps and the P/E stress-induced negative traps. Based on these four types of defects we can explain the endurance characteristics of two kinds of device. The switching property of pre-existing characteristic deep traps is also discussed.     

Comparison between N2 and O2 anneals on the integrity of an Al2O3/SiaN4/SiO2/Si memory gate stack

In this paper the endurance characteristics and trap generation are investigated to study the effects of different postdeposition anneals （PDAs） on the integrity of an Al2O3/Si3N4/SiOz/Si memory gate stack. The flat-band voltage （Vfb） turnarounds are observed in both the programmed and erased states of the N2-PDA device. In contrast, this turnaround is observed only in the erased state of the O2-PDA device. The Vfb in the programmed state of the O2-PDA device keeps increasing with increasing program/erase （P/E） cycles. Through the analyses of endurance characteristics and the low voltage round-trip current transients, it is concluded that in both kinds of device there are an unknown type of pre-existing characteristic deep traps and P/E stress-induced positive oxide charges. In the O2-PDA device two extra types of trap are also found： the pre-existing border traps and the P/E stress-induced negative traps. Based on these four types of defects we can explain the endurance characteristics of two kinds of device. The switching property of pre-existing characteristic deep traps is also discussed.     

Enhancing CO2 Separation Ability of a Metal–Organic Framework by Post‐Synthetic Ligand Exchange with Flexible Aliphatic Carboxylates

A series of porous metal–organic frameworks having flexible carboxylic acid pendants in their pores (UiO‐66‐ADn: n=4, 6, 8, and 10, where n denotes the number of carbons in a pendant) has been synthesized by post‐synthetic ligand exchange of terephthalate in UiO‐66 with a series of alkanedioic acids (HO₂C(CH₂)_n?2CO₂H). NMR, IR, PXRD, TEM, and mass spectral data have suggested that a terephthalate linker in UiO‐66 was substituted by two alkanedioate moieties, resulting in free carboxyl pendants in the pores. When post‐synthetically modified UiO‐66 was partially digested by adjusting the amount of added HF/sample, NMR spectra indicated that the ratio of alkanedioic acid/terephthalic acid was increased with smaller amounts of acid, implying that the ligand substitution proceeded from the outer layer of the particles. Gas sorption studies indicated that the surface areas and the pore volumes of all UiO‐66‐ADns were decreased compared to those of UiO‐66, and that the CO₂ adsorption capacities of UiO‐66‐ADn (n=4, 8) were similar to that of UiO‐66. In the case of UiO‐66‐AD6, the CO₂ uptake capacity was 34 % higher at 298 K and 58 % higher at 323 K compared to those of UiO‐66. It was elucidated by thermodynamic calculations that the introduction of flexible carboxyl pendants of appropriate length has two effects: 1) it increases the interaction enthalpy between the host framework and CO₂ molecules, and 2) it mitigates the entropy loss upon CO₂ adsorption due to the formation of multiple configurations for the interactions between carboxyl groups and CO₂ molecules. The ideal adsorption solution theory (IAST) selectivity for CO₂ adsorption over that of CH₄ was enhanced for all of the UiO‐66‐ADns compared to that of UiO‐66 at 298 K. In particular, UiO‐66‐AD6 showed the most strongly enhanced CO₂ uptake capacity and significantly increased selectivity for CO₂ adsorption over that of CH₄ at ambient temperature, suggesting that it is a promising material for sequestering CO₂ from landfill gas.     

我国乡镇邮政网点成本收入分析——来自4省(市)的61处乡镇邮政网点的调查

乡镇邮政网点的可持续运营是邮政服务三农、服务农村经济发展的重要保障.结合邮政网络运行特点,运用成本核算方法——作业成本法,建立乡镇邮政网点运营成本模型,并明确了间接成本的分摊依据和方法.实证分析了乡镇邮政网点的成本和收入情况,实证发现,我国乡镇邮政网点业务结构单一,普遍服务业务亏损严重,运营较为困难.最后为促进乡镇邮政网点可持续运营提供一些参考建议.     

Evaluation of the performance of post-Hartree-Fock methods in terms of intermolecular distance in noncovalent complexes

Dissociation curves calculated using multiple correlated QM methods for 66 noncovalent complexes (?ezá? et al., J Chem Theory Comput 2011, 7, 2427) have allowed us to interpolate equilibrium intermolecular distances for each studied method. Comparison of these data with CCSD(T)/complete basis set reference geometries provides information on how these methods perform in geometry optimizations. The large set of systems considered here is necessary for reliable statistical evaluation of the results and assessment of the robustness of the studied methods. Our results show that advanced methods such as MP3 and CCSD provide significant improvement over MP2 only when empirical scaling is used. The best results can be achieved with spin component scaled CCSD optimized for noncovalent interactions, with a root mean square error of 0.4% of the equilibrium distance. Scaled MP3, the MP2.5 method, yields comparably good results (error 0.5%) while being substantially cheaper. © 2011 Wiley Periodicals, Inc. J Comput Chem, 2012