双极结型晶体管的集电结反向雪崩击穿特性

通过气体放电产生更高浓度的低温等离子体要求具有纳秒上升沿和纳秒脉宽的高重频快脉冲,而目前被广泛使用的MOSFET和IGBT都无法满足这些参数要求,而双极结型晶体管(BJT）的集电极与发射极之间的雪崩击穿过程具有快导通、快恢复、高稳定性等优点,适合作为小型Marx发生器的自击穿开关。文中对用多种型号的BJT进行击穿特性比较测试实验,发现可以通过改变BJT的门极和发射极的并联电阻来调节其雪崩击穿电压,实现一定范围的工作电压。雪崩击穿恢复特性实验表明,当击穿电流衰减到低于维持电流时,BJT就会开始恢复绝缘而关断,通过改变电路中的参数以控制击穿电流的变化就可以控制BJT的雪崩击穿导通时间（即导通脉宽）。将这些结论应用到实际电路中,可获得上升沿5 ns、脉宽为10 ns、幅值2 kV、重复频率高达100 kHz的纳秒快脉冲,可用于激发高浓度低温等离子体。     

Excited electron-bubble states in superfluid 4He: a time-dependent density functional approach

We present a systematic study on the excited electron-bubble states in superfluid (4)He using a time-dependent density functional approach. For the evolution of the 1P bubble state, two different functionals accompanied with two different time-development schemes are used, namely an accurate finite-range functional for helium with an adiabatic approximation for electron versus an efficient zero-range functional for helium with a real-time evolution for electron. We make a detailed comparison between the quantitative results obtained from the two methods, which allow us to employ with confidence the optimal method for suitable problems. Based on this knowledge, we use the finite-range functional to calculate the time-resolved absorption spectrum of the 1P bubble, which in principle can be experimentally determined, and we use the zero-range functional to real-time evolve the 2P bubble for several hundreds of picoseconds, which is theoretically interesting due to the break down of adiabaticity for this state. Our results discard the physical realization of relaxed, metastable configurations above the 1P state.     

Synthesis,characterization, thermal and photophysical properties of novel strontium (II) phthalocyanine

Journal of Inclusion Phenomena and Macrocyclic Chemistry - Newly phthalocyanine derivative which carries 2,6-dimethoxyphenoxy bioactive groups as tetrakis from non-peripheral positions of the...     

Asymmetrically tetra-substituted phthalocyanine derivatives: synthesis,photophysical and photochemical properties

Transition Metal Chemistry - The syntheses of highly soluble asymmetrically substituted metal free and zinc phthalocyanine derivatives bearing three 4-(4-(5-phenyl-1,3,4-oxadiazol-2-yl)phenoxy) and...     

Mechanistic Investigation on Chemiluminescent Formaldehyde Probes

A first-generation pair of chemiluminescent formaldehyde (FA) probes (CFAP540 and CFAP700) was reported recently. CFAP540 and CFAP700, with high selectivity and sensitivity to FA, are, respectively, suitable in cell and in vivo. Experimentalists have confirmed that both probes utilize a general 2-aza-Cope FA-reactive trigger and a chemiluminogenic phenoxydioxetane scaffold. The mechanism and detailed process of CFAP chemiluminescence (CL) remain largely unknown. In the present paper, (time-dependent) density functional theory calculations are performed on the entire reaction process of CFAP540 with FA to produce CL. The calculations elucidated the CL-producing process: FA initiates the decomposition of CFAP540 by dehydration condensation, and a phenoxy 1,2-dioxetane is formed through a series of reactions of aza-Cope rearrangement, hydrolysis of imine, and β-elimination of alkoxyl group. Afterwards, the produced phenoxy 1,2-dioxetane decomposes to produce the m-oxybenzoate derivative in the first singlet state (S₁) via two crossings between potential energy surfaces of the ground state (S₀) and S₁ state. This m-oxybenzoate derivative was assigned as the light emitter of the CFAP540 CL. The CL-producing process and assignment of the light emitter of CFAP700 CL are similar with the corresponding ones of CFAP540. By analyzing the D-π-A architecture of the light emitters of CFAP540 and CFAP700, a series of CFAPs is theoretically designed and a scheme to modulate their CL from visible to near-infrared region is proposed by adjusting the length and structure of the π-bridge.