不同周期数的GaInAs/GaAsP多量子阱太阳能电池

为了研究不同量子阱周期数下GaInAs/GaAsP多量子阱太阳能电池性能的变化规律,利用金属有机化学气相沉积技术(MOCVD)制备了不同周期数的双结多量子阱太阳能电池样品以及无量子阱双结结构的参考样品,利用高分辨率X射线衍射仪(HXRD)和高分辨率透射电镜(TEM)测试了样品的晶体质量,同时在AM0(1×)光谱条件下测试了样品的I-V特性曲线和相应子电池的外量子效率。最终得到了高晶体质量、吸收截止波长在954 nm的Ga_(0.89)In_(0.11)As/GaAs_(0.92)P_(0.08)多量子阱结构,扩展波段的外量子效率最高达到75.18%,电池光电转换效率相对于无量子阱结构提升2.77%。通过对比测试结果发现,随着量子阱结构周期数的增加,太阳能电池在扩展波段(890~954 nm)的外量子效率不断提高,常规波段的短波响应(300~700 nm)会出现下降,长波响应(700~890 nm)会出现上升,短路电流和转换效率相应提升并趋于饱和。     

分布式抽运连续光纤激光器研究

为了避免高功率光纤激光器中光纤端面出现热效应问题,依据多点级联结构的耦合器,对分布式抽运的光纤激光器进行了研究。首先,介绍了实验室自主研制的级联耦合器。然后,分析了耦合器插入对光纤激光器的影响。最后,选用自制的耦合器搭建了分布式抽运的光纤激光器。实验结果表明:对耦合器插入损耗的研究,能够促进高功率级联耦合器的实现。在光纤激光器结构中,975 nm泵浦功率注入1.1 k W时,1 080nm激光功率输出为770 W,光-光转换效率为77%。在主控振荡功率放大结构中,激光功率输出为635 W,放大级的光-光转换效率为78%。分布式抽运方式可以使泵浦光多点注入,避免了热量的集中,能够获得千瓦级的激光功率输出。     

介质壁加速腔加速结构优化

为了在介质壁加速器中增大轴向加速电场, 提高加速梯度的同时抑制径向电场对束包络的扩张, 提出了在每个加速电极上添加金属栅网结构。采用基于粒子云网格方法的电磁粒子模拟软件对不加栅网与添加栅网的电极结构进行了数值仿真, 分析了不同结构下加速管道中的电场分布和束包络变化。通过实验对比了两种不同结构下经过相同的加速长度获得的粒子能量。结果表明:添加金属栅网结构相对于不加栅网的金属小孔式结构, 轴向加速电场强度提高20%, 同时径向电场得到有效抑制;栅网结构下, 被加速的粒子束在自由漂移空间中的径向发散基本得到抑制;在相同的加速长度下加速H3+粒子, 栅网结构得到的能量增益提高了一倍。     

介质壁直线加速器加速单元间的电路耦合及解耦

中国工程物理研究院流体物理研究所研发的介质壁直线加速器是基于固态脉冲形成线、GaAs光导开关和高梯度绝缘介质壁三项关键技术的新型直线脉冲加速器。在加速器调试阶段,测量出获得加速的质子束流能量远低于预期值,在排除功率源负载能力因素之后,发现脉冲功率源因连接回路引起的电路耦合效应是导致束流能量低的主要原因。基于介质壁直线加速器加速单元放电回路结构的分析,确认了加速单元之间的电路耦合的必然性。并通过测量回路电流,研究了几种不同工作模式下的电路耦合效应。结合电路耦合的特点,给出了两种基于磁芯隔离的解耦方法,并测量了这两种方法的解耦效率。     

甲醇在二氧化钛上的光化学性质与表面结构的相关性

通过双光子光电子的方法探测了TiO₂(011)-(2×1) 和TiO₂(110)-(1×1)表面的光催化氧化甲醇的性质. 在吸附了甲醇的二氧化钛(011)和(110)界面处探测到了一个费米能级以上2.5 eV的电子激发态,该电子激发态可作为测试二氧化钛界面还原性的探针使用. 利用此探针在甲醇/TiO₂(011)-(2×1)和甲醇/TiO₂(110)-(1×1)界面探测到了一个随光照时间的电子激发态信号变化,这一变化可以归于光催化生成的表面羟基对界面还原性的影响. 由此得出的光催化氧化甲醇的速率TiO₂(110)-(1×1)比TiO₂(011)-(2×1)快了大约11.4倍. 这可能由于表面原子结构排布的原因不同. 本工作不仅介绍了一个利用双光子光电子能谱探测到的甲醇/TiO₂界面电子结构的细节特征,还揭示了表面结构对二氧化钛光反应性质的重要影响.     

"Microfluidic drifting"--implementing three-dimensional hydrodynamic focusing with a single-layer planar microfluidic device

We introduce a novel fluid manipulation technique named "microfluidic drifting" to enable three-dimensional (3D) hydrodynamic focusing with a simple single-layer planar microfluidic device.     

Trapping of a dopaquinone intermediate in the TPQ cofactor biogenesis in a copper-containing amine oxidase from Arthrobacter globiformis

The biogenesis of the topaquinone (TPQ) cofactor of copper amine oxidase (CAO) is self-catalyzed and requires copper and molecular oxygen. A dopaquinone intermediate has been proposed to undergo 1,4-addition of a copper-associated water molecule to form the reduced form of TPQ (TPQ(red)), followed by facile oxidation by O(2) to yield the mature TPQ (TPQ(ox)). In this study, we have incorporated a lysine residue in the active site of Arthrobacter globiformis CAO (AGAO) by site-directed mutagenesis to produce D298K-AGAO. The X-ray crystal structure of D298K-AGAO at 1.7-A resolution revealed that a covalent linkage formed between the epsilon-amino side chain of Lys298 and the C2 position of a dopaquinone derived from Tyr382, a precursor to TPQ(ox). We assigned the species as an iminoquinone tautomer (LTI) of lysine tyrosylquinone (LTQ), the organic cofactor of lysyl oxidase (LOX). The time course of the formation of LTI at pH 6.8 was followed by UV/vis and resonance Raman spectroscopies. In the early phase of the reaction, an LTQ-like intermediate was observed. This intermediate then slowly converted to LTI in an isosbestic manner. Not only is the presence of a dopaquinone intermediate in the TPQ biogenesis confirmed, but it also provides strong support for the proposed intermediacy of a dopaquinone in the biogenesis of LTQ in LOX. Further, this study indicates that the dopaquinone intermediate in AGAO is mobile and can swing from the copper site into the active-site wedge to react with Lys298.     

Polyproline-rod approach to isolating protein targets of bioactive small molecules: isolation of a new target of indomethacin

Identification of protein targets of bioactive small molecules has been a technical hurdle of chemical genetics. Here we report a polyproline-rod approach to isolating protein targets of small molecules from cell lysates. The results indicate that insertion of a long, rigid polyproline helix between a small-molecule bait and a biotin tag boosts the capacity of affinity purification and thereby permits isolation of low-abundance or low-affinity proteins. In the course of the proof-of-concept experiments, we isolated glyoxalase 1 (GLO1) as a new target of indomethacin, a widely used antiinflammatory drug. Molecular biological experiments suggest that inhibition of GLO1 enzyme activity is related to the clinically recognized beneficial side effects of the indomethacin family of nonsteroidal antiinflammatory drugs.