基于FPGA的微型直流电机控制器IP核设计

为了实现阵列天线波束高效控制和系统小型化, 实现多轴微型直流伺服系统达到高速、并行控制, 根据Nios Ⅱ处理器的Avalon总线规范, 利用Verilog硬件描述语言, 设计了一种基于现场可编程逻辑门阵列(FPGA)的微型直流电机控制器IP核。该控制器采用了有限状态机的方法, 分多模块实现硬件控制功能。针对微型直流电机特性, 采用了比例-积分-微分（PID）算法、分段控制及启停监测等控制策略。最后利用软件Quartus Ⅱ及DE0开发板进行了仿真和实验验证, 实验表明, 该控制器具有响应速度快、定位精度高、可靠性高、体积小等特点, 可以可靠地对各路微型直流电机进行独立控制, 且控制性能良好, 能够实现天线单元快速、准确的相位控制。     

新型双阈值高g值MEMS惯性开关（英）

在保证引信勤务安全性和正常发射可靠性前提下,为实现引信小型化而设计了一种新型无源双阈值高g值MEMS惯性开关,其主要包括能够识别两种典型加速度环境（载荷1:15 000g-300 ms,载荷2：3000g-3 ms）的环境识别模块M1和为后续电路可靠供电的通电模块M2。环境识别模块M1主要通过控制带有Z型齿的质量块与对应L型挡块之间的碰撞来确定质量块的运动位移,进而控制通电模块M2的工作情况。基于两种典型加速度环境对MEMS惯性开关进行了动力学仿真并优化,仿真结果表明所设计的开关在载荷1环境下保持断开,而在载荷2环境下可靠闭合。     

严格电磁场波导方法的三维厚胶光刻工艺仿真（英）

无论是在微机电系统（MEMS）还是集成电路（IC）领域,SU-8厚胶光刻已经成为制造高深宽比结构的主流工艺。为了取代昂贵而耗时的光刻实验,一套能够良好预测显影形貌,从而为优化光刻制造提供有效帮助的光刻仿真软件就成为必要而有价值的工具。基于严格电磁场波导法的理论,给出一种针对SU-8光刻胶在紫外光下的三维光刻仿真模型。利用该模型,能很好地预测显影后的光刻胶内光强分布和立体形貌。并完成了一系列仿真和实验结果来验证模型的有效性。仿真结果给出横截面光强分布图和显影立体形貌模拟图形,并与相应的实验结果进行对照。结果验证了本文提出的仿真模型的正确性,并且表明三维混合模型在保证精确性的前提下,较之其他仿真算法运算速度更快。     

电除尘器的脉冲电源研究

为解决电除尘器脉冲电源存在的负载上脉冲拖尾、电容剩余电压积累、负载上电压振荡问题, 在充电二极管两端反向并联了一个辅助开关。详细分析了电路的工作原理, 给出了选取影响负载上脉冲波形的关键元器件参数的理论依据, 仿真分析和低压试验验证了解决方案的正确性。脉冲电源的改进, 有利于进一步提高除尘效率和能量利用率。     

热稳定单原子催化剂的理性构筑:从原子级结构到实际应用

80%以上的工业生产过程涉及催化,如化工生产、能源转换、制药和废物处理等等.催化剂的使用显著提高了生产效率,降低了生产成本,为国民经济、地球环境和人类文明的可持续发展做出了很大贡献.为了满足日益增长的生产需求和最大的经济效益,开发高效、稳定、低成本的新型催化剂已成为当务之急.金属中心负载在载体上的负载型金属催化剂因其较好的催化活性和相对较低的金属用量而受到广泛关注.研究发现,负载型结构可增强传热和传质并增加活性金属中心的分散度,从而影响催化性能.此外,负载金属的颗粒尺寸对催化剂的性能有很大影响.迄今为止,科学家们一直在通过减小金属颗粒尺寸和提高原子利用效率来提高催化剂的活性.原子级尺寸的颗粒通常表现出与大尺寸颗粒显着不同的物理和化学性质,而当活性位点的尺寸缩小到单个原子时,单原子催化剂的概念应运而生.对于单原子催化剂,金属原子中心通过配位被载体中的缺陷锚定,从而调整金属原子的电子云分布.这种配位调整使得单原子催化剂拥有与传统催化剂不同的性能.作为催化领域的新前沿,单原子催化剂已经在许多催化反应中表现出前所未有的活性和选择性.然而,许多报道的单原子催化剂在高温环境或长期催化应用中容易受到奥斯特瓦尔德熟化过程的影响,从而导致催化剂烧结和失活.而烧结的原因在于金属原子和载体之间较弱的相互作用.失活催化剂的再生和回收将大大增加工业生产的时间和经济成本.因此,开发具有优异热稳定性的单原子催化剂以满足工业需求是十分必要的.本综述首先总结了近年来关于热稳定型单原子催化剂合成方法的基础研究,并从原子尺度上分析了这些方法所构建的金属中心的结构形态和配位环境.此外,结合近些年的研究中新的表征技术与理论计算手段解释了热稳定性的来源.重点讨论了热稳定单原子催化剂的实际催化应用.分析了热稳定单原子催化剂在热催化应用中的独特作用机理、并尝试为确定催化过程中真正的活性中心以及通过原子级调控手段进行高活性热稳定单原子催化剂的合成提供理论指导.最后总结了热稳定单原子催化剂发展的主要问题,并简要分析了单原子催化领域的研究挑战和发展前景.     

Ultrabright AIEdots with tunable narrow emission for multiplexed fluorescence imaging

AIEgen doped fluorescent nanodots (AIEdots) have attracted lots of attention, due to their superior characteristics as fluorescent probes, such as excellent photostability, large Stokes shift, high brightness and tunable emission. Unfortunately, most of the currently available AIEdots exhibit broad emission bandwidth, which limits their applications in multiplexed fluorescence imaging and detection. In this work, the strategy of designing and fabricating narrow emissive AIEdots (NE-AIEdots) with tunable wavelengths was presented by constructing a light-harvesting system with high energy transfer efficiency. Efficient intra-particle energy transfer from highly doped AIEgens, serving as the light-harvesting antenna, to the lightly doped narrow emissive fluorophore, resulted in high brightness and narrow emission. The emission band of NE-AIEdots with the full-width-at-half-maximum varied from 18 to 36 nm was 3–6.3 times narrower than that of traditional AIEdots. The single-particle brightness of NE-AIEdots was over 5-times that of commercial quantum dots under the same excitation and collection conditions. Taking advantage of the superior performance of these NE-AIEdots, multiplexed fluorescence imaging of lymph nodes in living mice was realized, which supported the future applications of NE-AIEdots for in vivo multiplexed labeling and clinical surgery.

AIEdots with high brightness and narrow emission bandwidth were developed for multiplexed in vitro and in vivo fluorescence imaging.     

New lead-iodide formates with a strong second-harmonic generation response and suitable birefringence obtained by the substitution strategy

Nonlinear optical (NLO) crystals featuring a strong second-harmonic generation (SHG) response and suitable birefringence to achieve phase-matching are in urgent demand in industrial and commercial applications. Based on the substitution strategy, two new NLO lead-iodide formates, K₂[PbI₂(HCOO)₂] and Rb₂[PbI₂(HCOO)₂], have been successfully synthesized using a moderate mixed-solvothermal method. K₂[PbI₂(HCOO)₂] and Rb₂[PbI₂(HCOO)₂] exhibit strong phase-matching SHG responses of 8 and 6.8 × KDP, respectively, a suitable birefringence and transparent window covering most of the visible light and mid-IR region. Crystal structures and theoretical calculations unveil that the origins of the strong SHG response and suitable birefringence can be credibly attributed to the oriented arrangement of the highly distorted [PbI₂O₄] hexa-coordinated polyhedra, which are consistent in their local dipole moments, as well. This research provides a new strategy to explore high-performance NLO crystals.

K₂[PbI₂(HCOO)₂] and Rb₂[PbI₂(HCOO)₂] with highly distorted [PbI₂O₄] polyhedra in an oriented arrangement exhibit a very strong phase-matching SHG response, suitable birefringence, wide transparent windows and good thermal stability.     

Fluorine extraction from organofluorine molecules to make fluorinated clusters in yttrium MOFs

A new rare earth based two-dimensional coordination network and a three-dimensional metal–organic framework (MOF) have been synthesized using bicinchoninic acid (BCA) and yttrium(iii) ions. Yttrium dimer nodes are formed in the absence of a modulator, resulting in a 2D layered coordination network (Y–BCA-2D). The presence of fluorinating agents, e.g., 2-fluorobenzoic acid (2-FBA), 2,6-difluorobenzoic acid (2,6-DFBA), and perfluorohexanoic acid (PFHxA) result in μ₃-F bridged metal hexaclusters (Y₆F₈) that form a three-dimensional MOF (Y–BCA-3D). It was found that Y³⁺ can break highly stable C–F bonds in aromatic and aliphatic fluorinated compounds. Single-crystal X-ray diffraction (SC-XRD) shows the presence of fluorine in the metal cluster which was confirmed by energy dispersive X-ray spectroscopy (EDS). High resolution X-ray photoelectron spectroscopy (XPS) and ¹⁹F Nuclear Magnetic Resonance (NMR) also verify the presence of metal–fluorine bonds in the cluster. The Y–BCA-3D MOF selectively adsorbs CO₂ but not N₂.

The reaction of yttrium(iii) and linker makes a 2D metal–organic framework. The addition of fluorinated modulators result in fluorine extraction from modulators and makes a 3D-MOF.     

脉冲大电流放电引爆含能材料产生冲击波的储层改造

介绍了复合电热化学法产生冲击波的机理和冲击波改善储层物性的机制;给出了脉冲大电流引爆含能材料弹丸的结构和典型的放电参数,开展了冲击波致裂储层的实验研究;检测了样品在冲击作用下的动态应变及影响储层解吸附特性的关键参数（包括孔隙度、渗透率、抗拉、抗压强度等）,并在实验前后进行了测量和对比。研究表明,电热化学法产生的冲击波可在圆柱形砂岩样品上产生幅值为1000~1500的应变量,使砂岩出现了宏观裂缝;样品平均孔隙度由15.24%增至15.62%,平均渗透率由1.749 0910-3 m2增至2.467 0810-3 m2;抗压、抗拉和抗剪强度均下降了约30%。     

5 MA 100 ns重频LTD驱动器设计

设计了用于Z箍缩丝阵实验的重频LTD驱动器, 含6路并联模组, 每组由8个0.8 MA原型模块串联组成, 全真空结构。原型模块采用全新的单路触发和电感隔离技术, 触发难度和重频运行可靠性得到显著优化。利用电路模拟程序对驱动器进行了仿真计算, 结果表明：在初始半径1.2 cm、线质量1 mg/cm的Z箍缩负载上, 驱动器的输出电流峰值可到5.2 MA, 前沿91 ns;负载内爆最大动能78 kJ, 从电容储能至负载动能的转化效率为11.7%。该驱动器预期将获得高达20%~30%的辐射能量效率, 可为Z箍缩物理研究提供高效的实验平台。