光放大器前置可调光学滤波器

介绍Ｆ－Ｐ干涉滤波器实现中心波长可调的两种机理，给出通过改变腔距来改变中心波工的滤波器的典型结构，并且给出了相应的电压驱动电路，实验表明选择合适的光放大器前置滤波器可以提高系统的灵敏度。     

Two-Dimensional Supramolecular from the Self-Assembly of Dissymmetrical Oxamidato-Bridged Heterometallic Trinuclear Building Blocks: Synthesis, Crystal Structure, and Magnetic Properties

Two heterometallic trinuclear complexes {[Cu(oxbp)]₂Co(H₂O)₂}1.5DMF0.5H₂O (complex 1) and {[Cu(oxbm)]₂Co(H₂O)₂}2DMF (complex 2) were obtained from the self-organization of two new dissymmetrical oxamidato-bridged copper(II) building blocks [Cu(oxbp)]^– and [Cu(oxbm)]^–[H₃oxbp=N-benzoato-N'-(3-aminopropyl)oxamido, H₃oxbm=N-benzoato-N'-(2-amino-2-methylethyl)oxamido, DMF=dimethylformamide]. The crystal structure of complex 1 has been determined. Complex 1 crystallize in triclinic system, space group P-1, a=8.0609(16) Å, b=10.661(2) Å, c=22.279(5) Å, =85.32(3), =86.64(3), =70.90(3), and Z=1. The crystal structure of complex 1 consists of neutral trinuclear complex units, and hydrogen bond involved DMF and water molecules. Through the hydrogen bonds, weak coordination and CuCu weak interactions, complex 1 features a 2-D supramolecular structure. Magnetic susceptibility measurements (5–100 K) indicate that the central Co(II) and terminal copper metal ions are antiferromagnetically coupled with J=–28.09 and J=–29.70 cm^–1 for complex 1 and 2, respectively.     

Unraveling the Impact of Gold(I)–Thiolate Motifs on the Aggregation‐Induced Emission of Gold Nanoclusters

Aggregation‐induced emission (AIE) provides an efficient strategy to synthesize highly luminescent metal nanoclusters (NCs), however, rational control of emission energy and intensity of metal NCs is still challenging. This communication reveals the impact of surface Au^I‐thiolate motifs on the AIE properties of Au NCs, by employing a series of water‐soluble glutathione (GSH)‐coordinated Au complexes and NCs as a model ([Au₁₀SR₁₀], [Au₁₅SR₁₃], [Au₁₈SR₁₄], and [Au₂₅SR₁₈]^?, SR=thiolate ligand). Spectroscopic investigations show that the emission wavelength of Au NCs is adjustable from visible to the near‐infrared II (NIR‐II) region by controlling the length of the Au^I‐SR motifs on the NC surface. Decreasing the length of Au^I‐SR motifs also changes the origin of cluster luminescence from AIE‐type phosphorescence to Au⁰‐core‐dictated fluorescence. This effect becomes more prominent when the degree of aggregation of Au NCs increases in solution.     

分离式热管在机房空调系统中应用研究进展

介绍了分离式热管应用于数据机房空调系统的工作原理和技术特征,分析了充液率、高度差和温差等因素对分离式热管传热性能的影响,以及分离式热管与常规空调复合使用节能性的研究现状。目前,分离式热管系统提供的冷量只是对机房内的环境进行降温,不能对机房内发热设备直接降温,降低了冷量利用效率。针对这种情况,可以把微通道热管换热器置入发热设备内部,直接对发热设备进行降温。通过这种改进空调设备、优化气流组织的节能方法与手段,达到更加节能的目的。     

Dredging the Charge-Carrier Transfer Pathway for Efficient Low-Dimensional Ruddlesden-Popper Perovskite Solar Cells

Low-dimensional Ruddlesden-Popper (LDRP) perovskites still suffer from inferior carrier transport properties. Here, we demonstrate that efficient exciton dissociation and charge transfer can be achieved in LDRP perovskite by introducing γ-aminobutyric acid (GABA) as a spacer. The hydrogen bonding links adjacent spacing sheets in (GABA)₂MA₃Pb₄I₁₃ (MA=CH₃NH₃⁺), leading to the charges localized in the van der Waals gap, thereby constructing “charged-bridge” for charge transfer through the spacing region. Additionally, the polarized GABA weakens dielectric confinement, decreasing the (GABA)₂MA₃Pb₄I₁₃ exciton binding energy as low as ≈73 meV. Benefiting from these merits, the resultant GABA-based solar cell yields a champion power conversion efficiency (PCE) of 18.73 % with enhanced carrier transport properties. Furthermore, the unencapsulated device maintains 92.8 % of its initial PCE under continuous illumination after 1000 h and only lost 3 % of its initial PCE under 65 °C for 500 h.     

Single-crystalline layered double hydroxides with rich defects and hierarchical structure by mild reduction for enhancing the oxygen evolution reaction

The oxygen evolution reaction(OER) with sluggish reaction kinetics and large overpotential is the critical reaction in water splitting that is promising for energy storage and conversion. Layered double hydroxides(LDHs), due to their unique lamellar structure and flexibility of chemical component, are very competing material candidates for OER. Herein, the morphology structure and the electronic structure of LDHs were simultaneously tuned to improve the OER catalytic activity by mild solvothermal reduction using ethylene glycol. The increased surface area, the introduction of oxygen vacancies and the construction of hierarchical structure greatly enhanced the electro-catalytic activity of LDHs for OER. The as-prepared LDHs showed a lower over-potential as low as 276 mV at a current density of 10 mA cm~(-2), and a small Tafel slope of 40.3 mV dec~(-1) accompanied with good stability. This work provides an efficient way to the design and optimization of advanced catalysts in the future.     

Assemblies of a new flexible multicarboxylate ligand and d10 metal centers toward the construction of homochiral helical coordination polymers: structures, luminescence, and NLO-active properties

Hydro(solvo)thermal reactions between a new flexible multicarboxylate ligand of 2,2',3,3'-oxydiphthalic acid (2,2',3,3'-H(4)ODPA) and M(NO(3))(2).xH(2)O (M = Zn, x = 6; M = Cd, x = 4) in the presence of 4,4'-bipyridine (bpy) afford two novel homochiral helical coordination polymers [[Zn(2)(2,2',3,3'-ODPA)(bpy)(H(2)O)(3)].(H(2)O)(2) for 1 and [Cd(2)(2,2',3,3'-ODPA)(bpy)(H(2)O)(3)].(H(2)O)(2) for 2]. Though having almost the same chemical formula, they have different space groups (P2(1)2(1)2(1) for 1 and P2(1) for 2) and different bridging modes of the 2,2',3,3'-ODPA ligand. Two kinds of homochiral helices (right-handed) are found in both 1 and 2, each of which discriminates only one kind of crystallographical nonequivalent metal atom. 1 has a 2D metal-organic framework and can be seen as the unity of two parallel homochiral Zn1 and Zn2 helices, in which the nodes are etheric oxygen atoms. In contrast, 2 has a 3D metal-organic framework and consists of two partially overlapped homochiral Cd1 and Cd2 helices in the two dimensions. Moreover, metal-ODPA helices give a 2D chiral herringbone structural motif in both 1 and 2 in the two dimensions, which are further strengthened by the second ligand of bpy. Bulk materials for 1 and 2 all have good second-harmonic generation activity, approximately 1 and 0.8 times that of urea.     

Necklace-like hollow carbon nanospheres from the pentagon-including reactants: synthesis and electrochemical properties

Necklace-like hollow carbon nanospheres (CNSs) have been successfully synthesized from the pentagon-including reactants, which provide an auxiliary example for the theoretical prediction that necklace-like hollow CNSs are assumed to be composed of the regular occurrence of nonhexagonal rings at the atomic level. Benefits of the as-obtained hollow CNSs also arise from the high Brunauer-Emmett-Teller value of 594.32 m(2)/g and a narrow pore distribution at 5 nm. The electrochemical hydrogen storage experiments for the as-obtained necklace-like hollow CNSs exhibit a capacity of 242 mAh/g at the current density of 200 mA/g, corresponding to a hydrogen storage of 0.89 wt %, which is higher than the previously reported electrochemical capacities for the multiwalled carbon nanotubes (MWCNTs). Furthermore, the as-obtained necklace-like hollow CNSs show a lithium capacity advantage compared with the carbon solid particles for application in lithium batteries. These results indicate that the necklace-like hollow CNSs provide a new candidate for the application in hydrogen storage and lithium batteries.     

具有二维超分子结构的{[Ni(oxbe)]2Mg(H2O)2}·2DMF·DMA的合成及晶体结构

合成了一种中心对称的草酰胺桥联异三核配合物{[Ni(oxbe)]2Mg(H2O)2}·2DMF·DMA[oxbe为N-(2-羧基苯)-N'-(2-氨乙基)不对称草酰胺(H3oxbe)的脱氢阴离子;DMF为N,N-二甲基甲酰胺;DMA为二甲胺].用单晶X射线衍射法测定了它的晶体结构,该晶体属单斜晶系,空间群C2/e,晶胞参数a=22.617(5)A,b=17.173(4)A,c=10.881(4)A,β=115.40(2)°,V=3818(2)A3,Ni2MgC30H44N8O13,Mr=866.46,Z=4,Dc=1.508g/cm3,μ(MoKα)=1.075mm-1,F(000)=1808,R=0.0660,wR=0.1772(I＞2б(I)),3755个可观察衍射点.该三核分子为中心对称结构,镁离子位于6个氧原子所构成的变形八面体的中心,两个镍离子则分别位于两端由N3O构成的近似平面四方场中,中心Mg2+与两端的Ni2+通过草酰胺阴离子桥联在一起.     

泽泻科植物果实和果皮的微形态特征的分类学意义

用扫描电镜的方法对泽泻科所有属植物果皮的微形态进行了观察．结果表明Ｄａｍａｓｏｎｉｕｍ，Ｂａｌｄｅｌｉａ属具有蜡质附属物，仅Ｄａｍａｓｏｎｉｕｍ属果皮上有气孔器分布等特征可作为属间分类的重要依据．鉴于属内果皮微形态特征相似性程度较高，依据果实的形态及类型、表皮细胞的形状等特征作出了泽泻科１１属的分类检索表．初步探讨了果皮的微形态特征在泽泻科中的分类学意义，认为这一性状对该科属级水平的划分有重要的作用．