A 12-bit 300 MHz CMOS DAC for high-speed system applications

This paper describes a 12-bit 300 MHz CMOS DAC for high-speed system applications. The proposed DAC consists of a unit current-cell matrix for 8 MSBs and a binary-weighted array for 4 LSBs. In order to ensure the linearity of DAC, a double Centro symmetric current matrix is designed by using the Q(2) random walk strategy. To minimize the feedthrough and improve the dynamic performance, the drain of the switching transistors is isolated from the output lines by adding two cascoded transistors.

A direct digital frequency synthesizer with fourth-order phase domain Delta Sigma noise shaper and 12-bit current-steering DAC

This paper presents a direct digital frequency synthesizer (DDFS) with a 16-bit accumulator, a fourth-order phase domain single-stage Delta Sigma interpolator, and a 300-MS/s 12-bit current-steering DAC based on the Q(2) Random Walk switching scheme. The Delta Sigma interpolator is used to reduce the phase truncation error and the ROM size. The implemented fourth-order single-stage Delta Sigma noise shaper reduces the effective phase bits by four and reduces the ROM size by 16 times. The DDFS prototype is fabricated in a 0.35-mu m CMOS technology with active area of 1.11 mm(2) including a 12-bit DAC. The measured DDFS spurious-free dynamic range (SFDR) is greater than 78 dB using a reduced ROM with 8-bit phase, 12-bit amplitude resolution and a size of 0.09 mm(2). The total power consumption of the DDFS is 200)mW with a 3.3-V power supply.

12 W high efficiency single frequency ring laser

Single-frequency output power of 12 W at 1064 nm is demonstrated. Pumped by a fiber-coupled diode laser, the Nd:YVO4 produces 58.6% of the slope efficiency with respect to absorbed pump power, and 52.7% of the optical-optical efficiency and nearly diffraction-limited output with a beam quality parameter of M-2 approximate to 1.11. To the best of our knowledge, this is the highest slope efficiency and optical-optical efficiency in single-frequency Nd:YVO4 ring laser. The slope efficiency of the single frequency laser is close to the limit of the efficiency. [GRAPHICS] output spectrum of the single-frequency Nd:YVO4 ring laser

假单胞菌P_(12)对菲的降解

从武汉石油化工厂的活性污泥中，分离到一株可以以菲为唯一碳源和能源的假单胞菌P_(12)该菌经靛蓝产生法测定有双加氧酶，在菲无机盐培养基中生长时，有3-菲酚物质积累，经检测有一条质粒带。用丝裂霉素C消除质粒后的菌落，失去了降解菲的能力，说明P_(12)对菲的降解功能是由质粒控制的。

Pulse-front matched ultra-broadband optical parametric chirped pulse amplifier for sub-12 fs pulse generation

We propose a LBO-based ultra-broadband chirped pulse optical parametric amplifier employing pulse-front-matching to yield transform-limited sub-12-fs pulses. Measurement of the maximum possible gain bandwidth for the LBO-based OPCPA demonstrates more than 60nm gain bandwidth FWHM. For the generation of TL pulses by the use of this OPCPA, a suitable combination of OPCPA and PFM is first presented. The PFM pump geometry realizes tilt-free signal amplification, and permits this OPCPA to generate TL sub-12-fs pulses.

Cyanex302及CA-12萃取稀土动力学的研究

随着萃取技术的不断发展，人们日益要求更加深入的了解萃取过程的机制及其动力学特性。以便有效地控制和强化萃取过程，提高萃取效率，或者利用萃取动力学的差异来实现某些分离嘴过程。尽管许多萃取过程进行得很快，但是人们也发现不少的金属鳌合物萃取体系，其萃取过程相当缓慢。因而这类体系的萃取机制和萃取动力学问题已日益引人注目。除此而外，在设计，放大或改进萃取设备时，研究和掌握有关萃取过程的动力学规律也有十分重要意义。在本文中主要对稀土萃取动力学进行了研究，得到主要结果如下：1．研究了硫代有机磷酸Cyan.ex302萃取饵的动力学。通过测定各种萃取条件对萃取速率的影响，获得了萃取速率方程，并讨论了萃取的控制过程。实验发现萃取剂中的杂质对萃取具有较大的加速作用，这对工业生产具有一定的实际意义。2.用两相滴定法测定了两种新合成的J梭酸萃取剂CA-12和CA-100的某些重要的物理常数。这将有助于深入研究它们的萃取性质及机理。3．用层流恒界面池研究了CA-12萃取La, Gd,Er, Yb和Y的动力学。考察了各种因素对萃取速率的影响，获得了它们的萃取速率方程，实验发现了它们的萃取控速步骤并推测了其萃取机理。4．研究了HEHEHP对CA-12萃取Yb和Y的动力学的影响。实验发现在CA一12中加入少量的HEHEHP后，萃取活化能显著降低，萃取速率明显加快。由于加入HEHEHP后，萃取Yb的活化能的降低要比萃取Y的活化能降低的程度大'，所以使Yb和Y的萃取分离因素加大。5．用两相滴定法研究了HEHEHP萃取铭的机理，CA-12萃取稀土及其相关离子的机理。并计算了它们相应的平衡常数。

环戊二烯基轻稀土氯化物的合成及其稳定性的研究

I LnCl_3-LiCl-THF配合物的研究深入地研究了氯化稀土和氯化锂于四氢呋喃溶液中，以不同的摩尔比，在不同条件下的反应。实验结果表明，反应速度随着稀土元素原子半径的减小，LiCl/LnCl_3摩尔比的增大，以及四氢呋喃用量的增加而加快。通过紫外质谱元素分析和X-射线单晶结构分析等证明，随着不同的LiCl/LnCl_3摩尔比和结晶条件的不同，可以得到不同组成的LnCl_3-LiCl-TNF配合物。对(LaCl)(THF)_2(μ_2-Cl)_4[Li(THF)_2]_2和(LaCl)DME(μ_3-Cl)(μ_2-Cl)_5(La·DME)Li(THF)_2晶体的结构分析表明，前者为单斜晶系，P21/C空间群。a=10.542(4), b=32.236(4), c=11.182(6)A °; β=113.50(3) °, V=3484.97 A °~3. Z=4, R=0.0471；后者为三斜晶系，PT空间群，晶胞参数是：a=11.123(3), b=16.564(5), c=8.653(3)A °;α=95.16(3), β=95.63(3), γ=74.71(3) °;V=1527.0A °~3。Z=2，R=0.0303。实验结果还表明，μ_2-和μ_3-氯桥键是LnCl_3-LiCl-THF类配合物中最基本、最重要的配位键，这种键是通过多重键的方式起着稳定分子结构的作用。当进行与有机配体的交换反应时，由于它们的特殊稳定性，能起到阻止轻稀土有机配合物歧化反应的作用。II环戊二烯基轻镧系氯化物的合成及其稳定性的研究对(G_5H_5)_3Ln·THF和LnCl_3·3LiCl-THF (Ln=La, Nd)溶液反应的研究表明，由于μ_2-氯桥键的作用，轻稀土环戊二烯基化合物中环戊二烯基的再分配反应，在0℃或室温下都能迅速进行。通过两者不同的摩尔比反应，经元素分析、红外光谱、~1H NMR和质谱鉴定，方便地合成了C_5H_5 LnCl_2·2LiCl·5THF和(C_5H_5)_2LnCl.LiCl·nTHF (Ln=La, Nd)等配合物。这一结果表明(C_5H_5)_2LnCl.LiCl·nTHF配合物不仅能稳定地存在于THF溶液中，而且能在一定条件下析出结晶。对(C_5H_5)_2LaCl.LiCl·4THF的晶体结构测定表明，该晶体属于正交晶系，Pc2m空间群。a=12.306(4), b=23.056(6), c=26.701(11)A°; V=7575.81A°~3;而(C_5H_5)_2LaCl·LiCl(DME)_2THF晶体则属于六方晶系，a=12.967(4), b=12.967(4), c=24.108(10)A°;V=3510 A°~3。通过(G_5H_5)_3Ln·THF与LnCl_3·3THF (Ln=La, Nd)的反应进一步研究了轻稀土环戊二烯基氯化物的稳定性。经元素分析，红外光谱和晶体结构分析表明合成了[(η~5-C_5H_5)_4La_3Cl_5·3THF]_2·9THF和(C_5H_5)_2 NdCl·THF配合物，前者属于三斜晶系，P1空间群。a=11.690(3), b=11.750(5), c=18.433(6)A°; α=98.75(3), β=95.62(3), γ=118.92(2)°; V=2147.06 A°~3. Z=1, R=0.099。对环戊二烯基轻稀土氯化物的稳定性进行了较详细地讨论。结果表明，THF的用量和化合物的溶解度是影响产物组成的决定因素。当THF的量不足以溶解所生成的产物时，就会歧化成溶解度最大((C_5H_5)_3Ln·THF)和最小(LnCl_3·nTHF)的两种组分。反之，环戊二烯基轻稀土化合物(Ln=La, Nd)中环戊二烯基的再分配反应就能顺利进行。经元素分析和结构测定，在((C_5H_5)_3Nd·THF)和NdCl_3·LiCl-THF溶液的反应体系中，偶然分离得到了[(η~5-C_5H_5)_4Nd_4(μ_4-o)(μ_2-Cl)_8] [Li(DMP)_2THF]_2这一不合常规的化合物，其晶体属于正交晶系，Pna2,空间群a=19.010(7), b=23.231(6), c=14.180(4); V=6261.91 A°~3。Z=4, R=0.054。说明在一定条件下,μ-氧桥键也起到了稳定分子结构的作用。推测了各类环戊二烯基轻稀土氯化物在THF中的合成反应机理,在LiCl存在的反应体系中Ln cl cl Li桥键能与环戊二烯基发生交换反应;在(C_5H_5)_3Ln·THF和LnCl_3·3THF的反应体系中,首先存在着LnCl_3分子之间的互相作用，因而易于形成双核或多核配合物。这类配合物以晶体形式析出时，易于发生结构上的变化，即化合物的结晶形态与溶液中的形态不一定相同。探索了环戊二烯基烯丙基稀土化合物新的合成方法。找到了真空加热脱水制备氯化稀土的最佳条件，其产物纯度在97%以上。通过加入Co_3O_4/Wo_3催化助燃剂的方法，提高了测定稀土有机化合物中碳含量的准确性。

Co(salen)作为辅酶B_(12)模型物及化学修饰电极的电化学研究

本论文从合成Co(salen)开始，对Co(salen)在电化学现场合成辅酶B_(12)模型物的工作进行了尝试。进一步地，用Co(salen)制作了两种化学修饰电极，并对它们的性质进行了较为详细的考察。同时还将这两种修饰电极应用于电催化研究工作，得到了较为满意的结果。

The structures and transformations on Si(113) surface

The surface structures of the Si(113)-(1 X 1), Si(113)-(3 X 1) and Si(113)-(3 X 2) have been studied theoretically by means of an ab initio quantum chemical CNDO method. We address not only the importance of the surface energy but also the energy minimization and the barrier height in the different structural conversion. We found that (1) the relaxed Si(113)-(1 X 1) structure. (2) the Si(113)-(3 X 1) close to the Si(113) Ranke (3 X 1)-2 model; (3) the atomic positions of Si(113)-(3 X 2) corrugated arrangement. (C) 1997 Elsevier Science B.V.

Long period two-dimensional gratings for 8-12 mu m quantum well infrared photodetectors

By considering all possible high order diffracted waves, the authors investigate the spectral response of two-dimensional gratings for quantum well infrared photodetectors (QWIPs). A new method is proposed that using long period gratings may improve grating quality and reduce the resulting cross talk in grating-coupled QWIPs. A sensitivity analysis indicates that the influence of variation of the grating constant on the coupling efficiency is less sensitive for the long period gratings than for the short ones. A large coupling efficiency has been demonstrated for long period gratings. The calculated wide grating response spectra are in good agreement with the experiment result. (C) 1996 American Institute of Physics.

Hydrogen adsorption induced surface reconstructions on Si(113) studied by LEED

Surface reconstructions on Si(113) induced by dissociated hydrogen adsorption have been studied using low energy electron diffraction (LEED). It has been found that: (1) at 300 K and 80 K temperatures, with the increase of hydrogen coverage on the surface, the (3 x 1) phase transferred continuously into a hydrogen saturated (1 x 1)-2H phase; (2) flashing of the (1 x 1)-2H surface at about 1100 degrees C resulted in a complete new phase of(1 x 3) and further annealing of the sample at 1250 degrees C gave back the starting surface of (3 x 1); (3) saturated hydrogen adsorption at a sample temperature of 700 degrees C resulted in a stable new phase of(1 x 2)-H and further saturation doses of hydrogen at other temperatures below 700 degrees C did not change the (1 x 2) LEED pattern; (4) annealing of the (I x 2)-H surface in the same manner as (2) gave similar results.