Two-photon Dissociation Study of Carbon Disulfide in Acetonitrile at 266 nm

Using laser flash photolysis/transient absorption technique for the study of two photon photodissociation of carbon disulfide in acetonitrile solution at 266 nm, the transient UV-Vis absorption spectrum of Rydberg state CS2 （6sσg） within 240-370 nm and subsequent dissociation product CS （α^3П） with the maximum absorption at 260 nm were directly observed. The lifetime of CS （α^3П） in the nitrogen and oxygen saturated solution is also studied in our experiment.     

太赫兹电磁波大气吸收衰减逐线积分计算

大气对太赫兹辐射传输存在一定的非协作性,即存在吸收衰减。为了实现太赫兹辐射的有效应用必须细致地了解太赫兹辐射大气传输的窗口位置、宽度及大气透过率。选取了处理大气非均匀路径、吸收带重叠等大气辐射传输问题的最精确方法逐线积分法,发展计算程序,并基于HITRAN分子谱线数据,对水汽、氧气、臭氧、氮气、二氧化碳等单组分气体分子对太赫兹辐射传输的吸收衰减情况进行了计算与分析,并给出了在太赫兹电磁波大气传输衰减中占主要因素的水汽和氧气的衰减峰位置。     

斜波导喇曼振荡器

 采用斜波导的喇曼氢气池, 使泵浦激光束在波导内部传播, 增大了受激喇曼散射的作用区域。在传播过程中光束截面逐渐被压缩, 补偿因波导内壁的反射损耗而引起的功率密度下降。在一定气压范围内提高了喇曼转换的效率, 并利用波导对激光束的均匀作用, 使输出的一阶斯托克斯光光强的均匀性获得改善。     

The Cu-MOF-199/single-walled carbon nanotubes modified electrode for simultaneous determination of hydroquinone and catechol with extended linear ranges and lower detection limits

A novel electrochemical sensor based on Cu-MOF-199 [Cu-MOF-199 = Cu₃(BTC)₂ (BTC = 1,3,5-benzenetricarboxylicacid)] and SWCNTs (single-walled carbon nanotubes) was fabricated for the simultaneous determination of hydroquinone (HQ) and catechol (CT). The modification procedure was carried out through casting SWCNTs on the bare glassy carbon electrode (GCE) and followed by the electrodeposition of Cu-MOF-199 on the SWCNTs modified electrode. Cyclic voltammetry (CV), electrochemical impedance spectroscopy (EIS) and scanning electron microscopy (SEM) were performed to characterize the electrochemical performance and surface characteristics of the as-prepared sensor. The composite electrode exhibited an excellent electrocatalytic activity with increased electrochemical signals towards the oxidation of HQ and CT, owing to the synergistic effect of SWCNTs and Cu-MOF-199. Under the optimized condition, the linear response range were from 0.1 to 1453 μmol L⁻¹ (R_HQ = 0.9999) for HQ and 0.1–1150 μmol L⁻¹ (R_CT = 0.9990) for CT. The detection limits for HQ and CT were as low as 0.08 and 0.1 μmol L⁻¹, respectively. Moreover, the modified electrode presented the good reproducibility and the excellent anti-interference performance. The analytical performance of the developed sensor for the simultaneous detection of HQ and CT had been evaluated in practical samples with satisfying results.     

基于分数导数研究高强度聚焦超声的非线性声场

在高强度聚焦超声(high intensity focused ultrasound, HIFU) 的研究中, 生物组织的衰减和色散性质会对声能量的空间分布产生影响. 本文提出应用分数导数修正非线性Khokhlov-Zabolotskaya-Kuznetsov (KZK)方程, 研究生物组织中非线性HIFU声场. 对三种生物仿体的衰减和声速色散的理论实验研究表明分数导数应用的可行性, 在此基础上通过数值仿真分析研究了衰减及声速随频率的变化对HIFU焦域分布的影响. 研究结果表明, 在计算强非线性聚焦超声时, 由于高次谐波的强色散作用, 引入分数导数来解决生物组织特殊的衰减以及色散问题可进一步提高HIFU治疗的安全性. 关键词： 分数导数 声衰减 色散 高强度聚焦超声     

Simultaneous Magneto-Optical Trapping of Fermionic ^40K and Bosonic ^87Rb Atoms

We report on simultaneous magneto-optical trapping of fermionic ^40K and bosonic 87Rb atoms. This trap is the first step towards quantum degenerate fermi gas ^40K. Laser lights for the two-species magneto-optical trap （MOT） are generated from diode lasers and tapered amplifier. The enriched ^40K dispenser is utilized in the experimental setup. We obtain up to 10^7 -10^8 ^40K and 10^8 -10^9 ^87Rb atoms respectively in the steady-state single-species MOT.     

太赫兹互补金属氧化物半导体场效应管探测器理论模型中扩散效应研究

针对基于经典动力学理论传统模型中忽略扩散效应的问题,通过对基于玻尔兹曼理论的场效应管传输线模型的理论分析,建立了包含扩散效应的太赫兹互补金属氧化物半导体(CMOS)场效应管探测器理论模型,研究扩散效应对场效应管电导及响应度的影响.同时,将此模型与忽略了扩散效应的传统模型进行了对比仿真模拟,给出了两种模型下的电流响应度随温度及频率变化的差别.依据仿真结果,并结合3σ原则明确了场效应管传输线模型中扩散部分省略的依据和条件.研究结果表明:扩散部分引起的响应度差异大小主要由场效应管的工作温度及工作频率决定.其中工作频率起主要作用,温度变化对差异大小影响较为微弱;而对于工作频率而言,当场效应管工作频率小于1 THz时,模型中的扩散部分可以忽略不计;而当工作频率大于1 THz时,扩散部分不可省略,此时场效应管模型需同时包含漂移、散射及扩散三个物理过程.本文的研究结果为太赫兹CMOS场效应管理论模型的精确建立及模拟提供了理论支持.     

Waveform preservation of the backscattered stimulated Brillouin scattering wave by using a prepulse injection

We have found that it is possible to preserve the temporal waveform of the reflected wave generated from stimulated Brillouin scattering (SBS) by using a prepulse technique. The waveform of the SBS wave usually shows a steep rising edge in the ordinary SBS process. It has been found that the waveform of the reflected wave depends on both the prepulse energy and the time delay between the main pulse and the prepulses. A prepulse energy of 5 mJ and a time delay of 5 ns have been measured to be the optimum values under the experimental conditions. This prepulse method is useful in developing a multistage system employing several SBS cells in series for high-power laser applications.     

Preparation of 2-pyridone-containing tricyclic alkaloid derivatives as potential inhibitors of tumor cell proliferation by regioselective intramolecular N- and C-acylation of 2-pyridone

A novel and practical preparation of 2-pyridone-containing tricyclic alkaloid derivatives was developed. By regioselective intramolecular N- and C-acylation of 2-(4-aryl-2-pyridon-6-yl)benzoic acid, a pair of structural isomers 2-aryl pyrido[2,1-a]isoindole-4,6-diones and 4-aryl 1-methyl-1H-indeno[1,2-b]-pyridine-2,5-diones, as potential inhibitors of tumor cell proliferation, were prepared respectively.     

Rapid and Sensitive Determination of Dinotefuran Residue Based on Electrochemical Enhancement of β‐cyclodextrin‐Graphene Composite

A rapid method for sensitive voltammetric determination of dinotefuran residue was reported. The proposed method was based on the electrocatalytic reduction of dinotefuran on β‐cyclodextrin‐graphene composite modified glassy carbon electrode (β‐CD‐rGO/GCE), giving rise to a higher reduction signal to dinotefuran relative to the bare (GCE) and graphene modified electrode (rGO/GCE). Moreover, a further signal enhancement was observed when the modified electrode incubated in solution at low temperature (0 °C) for a short time. The reduction mechanism and binding affinity were also discussed. The external standard calibration curve was obtained from linear sweep voltammetry in the range of 0.5 to 16.0 μM with a detection limit of 0.10 μM. In addition to optimization of pretreatment, this electrochemical method has been applied to the dinotefuran residue determination in millet samples with the detection limit of 0.01 mg kg^?1 and compared with an high performance liquid chromatography method. The proposed electrode and analysis methods were proven to be sensitive, accurate and rapid under the used conditions.