以硅片线锯屑和石英为原料合成氮氧化硅粉体研究

研究了以回收提纯的太阳电池硅片线锯屑粉与粗粒石英粉为原料直接用N2气体氮化合成氮氧化硅(Si2N2O)的工艺条件,分析原料配比和反应温度对氮氧化合成产物的影响.结果表明,采用这种线锯硅屑粉为原料,可以在1450℃下4h常压纯氮合成条件下得到氮氧化硅产物;当原料摩尔比n(Si)/n(SiO2)=1.5时,所得产物在XRD检测能力范围显示为纯Si2N2O相,不含氮化硅副产物相.从反应相对增重量分析推测,反应体系中可能包含SiO2在高温和低氧分压条件下的转变为Si2N2O的过程.     

SHF频段超宽带高温超导滤波器的研制

针对超宽带通信系统的发展趋势,采用1/4波长短截线结构设计了一个工作于超高频(SHF)频段的超宽带高温超导滤波器,滤波器的中心频率为4.2 GHz,相对带宽为50%,讨论了1/4波长短截线结构滤波器的设计原理,给出了所设计超宽带滤波器的理论曲线、模拟仿真结果。实际制作的超宽带高温超导滤波器的测量曲线与模拟仿真曲线基本吻合,得到了满意的结果。     

Monolayer organic field-effect transistors

Monolayer organic field-effect transistors(OFETs) are attracting worldwide interest in device physics and novel applications due to their ultrathin active layer for two-dimensional charge transport. The monolayer films are generally prepared by thermal evaporation, the Langmuir technique or self-assembly process, etc., but their electrical performance is relatively lower than corresponding thick films. From 2011, the performance of monolayer OFETs has been boosted by using the monolayer molecular crystals(MMCs) as active channels, which opened up a new era for monolayer OFETs. In this review, recent progress of monolayer OFETs, including the preparation of monolayer films, their OFET performance and applications are summarized.Finally, perspectives of monolayer OFETs in the near future are also discussed.     

Magnetic and Luminescence Properties of Two Dinuclear Lanthanide Complexes with Butterfly‐like Arrangement

Two dinuclear lanthanide complexes with pentadentate ligand 3‐[bis(pyridine‐2‐ylmethyl)amino]propane‐1,2‐diol (H₂L), formulated as [Ln₂(HL)₂(NO₃)₂(H₂O)₂] · 1.5NO₃ · 0.5I [Ln = Tb ( ZTU‐1 ) and Eu ( ZTU‐2 ); ZTU = Zhaotong University] were synthesized and structurally characterized. ZTU‐1 and ZTU‐2 are isomorphous and feature a butterfly‐like arrangement. The fluorescence properties of ZTU‐1 and ZTU‐2 are investigated and slow magnetic relaxation behavior is observed in ZTU‐1 .     

Large‐Scale,Bottom‐Up Synthesis of Binary Metal–Organic Framework Nanosheets for Efficient Water Oxidation

Ultrathin metal–organic framework (MOF) nanosheets (NSs) offer potential for many applications, but the synthetic strategies are largely limited to top‐down, low‐yield exfoliation methods. Herein, Ni–M–MOF (M=Fe, Al, Co, Mn, Zn, and Cd) NSs are reported with a thickness of only several atomic layers, prepared by a large‐scale, bottom‐up solvothermal method. The solvent mixture of N,N‐dimethylacetamide and water plays key role in controlling the formation of these two‐dimensional MOF NSs. The MOF NSs can be directly used as efficient electrocatalysts for the oxygen evolution reaction, in which the Ni–Fe–MOF NSs deliver a current density of 10 mA cm^?2 at a low overpotential of 221 mV with a small Tafel slope of 56.0 mV dec^?1, and exhibit excellent stability for at least 20 h without obvious activity decay. Density functional theory calculations on the energy barriers for OER occurring at different metal sites confirm that Fe is the active site for OER at Ni–Fe–MOF NSs.     

Charge Polarization from Atomic Metals on Adjacent Graphitic Layers for Enhancing the Hydrogen Evolution Reaction

Atomic metal species‐based catalysts (AMCs) show remarkable possibilities in various catalytic reactions. The coordination configuration of the metal atoms has been widely recognized as the determining factor to the electronic structure and the catalytic activity. However, the synergistic effect between the adjacent layers of the multilayered AMCs is always neglected. We reported an atomic Co and Pt co‐trapped carbon catalyst, which exhibits a ultrahigh activity for HER in the wide range of pH (η₁₀=27 and 50 mV in acidic and alkaline media, respectively) with ultralow metal loadings (1.72 and 0.16 wt % for Co and Pt, respectively), which is much superior to the commercial Pt/C. Theoretical analysis reveals that the atomic metals on the inner graphitic layers significantly alter the electronic structure of the outmost layer, thus tailoring the HER activity. This finding arouses a re‐thinking of the intrinsic activity origins of AMCs and suggests a new avenue in the structure design of AMCs.     

基于双折射晶体的快拍穆勒矩阵成像测偏原理分析

针对传统穆勒矩阵成像测偏仪包含活动部件,需进行多次测量,容易产生测量误差,不能对运动目标或动态场景进行同时、实时测量等问题,提出了一种以改进型萨瓦偏光镜为核心分光器件的快拍Mueller矩阵成像测偏技术(MSP-SMMIP).它不含任何活动部件,能通过单次快拍测量获取目标强度图像和全部16个穆勒矩阵阵元图像.它主要由偏振态产生和偏振态分析两部分组成,偏振干涉条纹通过偏振态产生光路后定位于测试样品上,随后这些条纹通过空间载频将样品的Mueller矩阵分量编码,经偏振态分析光路成像于焦平面上.采用斯托克斯矢量-穆勒矩阵形式阐明了光场偏振态被MSP-SMMIP调制的过程,给出了其像面干涉图表达式,讨论了Mueller矩阵反演和系统定标的方法.基于CCD相机参数分析了系统的光学指标.通过数值模拟实验给出模拟测量结果,通过定性和定量评价测量结果表明该系统的可行性.MSP-SMMIP技术具有稳态、快拍、结构简洁、易定标、可同时实时获取目标强度图像和全部Mueller矩阵阵元图像的显著特点.     

Semi-Quantum Private Comparison Using Single Photons

Recently, by using the BB84 quantum key distribution (QKD) protocol, Sun et al. put forward two quantum private comparison (QPC) protocols with a semi-honest third party (TP) and a malicious TP, respectively (Sun et al., Quantum Inf. Process. 14, 2125–2133, 2015). In this paper, we absorb the concept of semi-quantumness suggested by Boyer et al. (Phys. Rev. Lett. 99(14), 140501, 2007 and Phys. Rev. A 79(3), 032341, 2009) into Sun et al.’s QPC protocols and construct two corresponding SQPC protocols. The common interesting feature of the proposed SQPC protocols is that apart from the establishment of shared keys between different participants, the rest parts of the protocols are completely classical. The output correctness and the security of the proposed SQPC protocols are validated. Compared with the present SQPC protocols, the advantages of the proposed SQPC protocols lies in the following aspects: on the aspect of quantum resource, they employ single photons rather than Bell entangled states; with respect to quantum measurement for TP, they need single-photon measurements rather than Bell state measurements; as for quantum entanglement swapping, they do not need it at all; and the second proposed SQPC protocol takes effect under a malicious TP and makes TP know neither the genuine contents of secret inputs nor the comparison result.     

醇类化合物热值改进剂结构和性质的理论研究

采用Materials Studio8.0软件中的DMol3程序对醇类化合物热值改进剂的几何结构和性质(振动频率、反应活性、热力学及稳定性)进行了理论研究,得到了分子稳定的几何构型、各原子上的电荷分布、热力学性质、Fukui指数和前沿分子轨道能级.计算结果表明:醇类化合物热值改进剂分子结构中的1个-OH是影响其抗氧化活性的主要部位和亲电反应发生的活性位点,整体表现为比较理想的稳定性能.