MoO_3电致变色薄膜的XPS研究

近年来 ,随着人们提倡节能和使用洁净能源 ,无机电致变色材料在建筑物采光控制系统和反射率可调表面的应用研究 ,已成为材料领域的一个新热点 .WO3、 MoO3等过渡金属氧化物薄膜具有良好的电致变色效应 ,是人们研究的重点 .其中 MoO3的电致变色效果要好于 IrO2、 TiOx、 CoO及 NiOx等电致变色材料 [1],而且它在可见光区有比 WO3更柔和的色彩 ,使人眼更易于适应其颜色变化 .着色态的 MoO3称为钼青铜 ,其开路记忆也好于钨青铜 [2].故 MoO3电致变色薄膜是极有潜力用于实用化的电致变色器件 .MoO3薄膜常用的制备方法有真空蒸 发、化学气…     

Co(II) and Ni(II) complexes with imidazole-containing ligands: Synthesis,structural characterization,and magnetic property

Hydrothermal reaction of Co(II) salt with 1,4-di(1-imidazolyl)benzene (L¹) and 4,4’-oxydiphthalic acid (H₄OA) yields a new complex [Co₃(HOA)₂(L¹)₄(H₂O)₄] (I). [Ni(L²)₂SO₄] · 0.5H₂O (II) can be obtained via the hydrothermal reaction of NiSO₄ · 6H₂O with 1,3-di(1H-imidazol-4-yl)benzene (L²). Complexes I and II have been characterized by single-crystal and powder X-ray diffraction (CIF files CCDC nos. 1019291 (I) and 1019292 (II)), IR, elemental, and thermogravimetric analyses. Complex I exhibits the uninodal six-connected 3D pcu framework structure of I with (4¹² · 6³) topology; Complex II consists of the uninodal four-connected 2D sql (4⁴ · 6²) networks. In addition, magnetic property of I was investigated.     

Diversity synthesis of complex pyridines yields a probe of a neurotrophic signaling pathway

Recognizing the value of including complex pyridines in small-molecule screening collections, we developed a previously unexplored [2 + 2 + 2]-cycloaddition of silyl-tethered diynes with nitriles. The tether provides high regioselectivity, while the solvent THF allows catalytic CpCo(CO)(2) to be used without exogenous irradiation. One of the resulting bicyclic and monocyclic (desilylated) pyridines was identified as an inhibitor of neuregulin-induced neurite outgrowth (EC(50) = 0.30 microM) in a screen that probes a pathway likely to be involved in breast cancers and schizophrenia.     

Self-assembled double-shelled ferrihydrite hollow spheres with a tunable aperture

Novel double-shelled hierarchical ferrihydrite hollow spheres (Fe(10)O(14)(OH)(2).4H(2)O) were successfully synthesized on a large scale by using a facile medicine-inspired solution-phase approach. Sodium nitroprusside (SNP), an ordinary and inexpensive medicine for expanding blood vessels, served as both a ferric source and an in situ formed gas-bubble template with the presence of sodium dihydrogen phosphate as a pH regulator, coordinator, and stabilizer. A twice-gas-bubble template model has been proposed for the formation of the double-shelled hollow spheres to take advantage of the dissociation and hydrolyzation of the two kinds of ligands in the SNP precursor. The size of the double-shelled ferrihydrite hollow spheres can be tuned by varying the experimental parameters. As-obtained ferrihydrite is highly sensitive to ethanol gas, which indicates potential applications in the field of sensing devices.     

A General and High‐Yield Galvanic Displacement Approach to Au?M (M=Au,Pd, and Pt) Core–Shell Nanostructures with Porous Shells and Enhanced Electrocatalytic Performances

In this work, we utilize the galvanic displacement synthesis and make it a general and efficient method for the preparation of Au? M (M=Au, Pd, and Pt) core–shell nanostructures with porous shells, which consist of multilayer nanoparticles. The method is generally applicable to the preparation of Au? Au, Au? Pd, and Au? Pt core–shell nanostructures with typical porous shells. Moreover, the Au? Au isomeric core–shell nanostructure is reported for the first time. The lower oxidation states of Au^I, Pd^II, and Pt^II are supposed to contribute to the formation of porous core–shell nanostructures instead of yolk‐shell nanostructures. The electrocatalytic ethanol oxidation and oxygen reduction reaction (ORR) performance of porous Au? Pd core–shell nanostructures are assessed as a typical example for the investigation of the advantages of the obtained core–shell nanostructures. As expected, the Au? Pd core–shell nanostructure indeed exhibits a significantly reduced overpotential (the peak potential is shifted in the positive direction by 44 mV and 32 mV), a much improved CO tolerance (I_f/I_b is 3.6 and 1.63 times higher), and an enhanced catalytic stability in comparison with Pd nanoparticles and Pt/C catalysts. Thus, porous Au? M (M=Au, Pd, and Pt) core–shell nanostructures may provide many opportunities in the fields of organic catalysis, direct alcohol fuel cells, surface‐enhanced Raman scattering, and so forth.     

Vertically constrained CO2 retrievals from TCCON measurements

Partial column-averaged carbon dioxide (CO₂) mixing ratio in three tropospheric layers has been retrieved from Total Carbon Column Observing Network (TCCON) spectra in the 1.6 μm CO₂ absorption band. Information analysis suggests that a measurement with ～60 absorption lines provides three or more pieces of independent information, depending on the signal-to-noise ratio and solar zenith angle. This has been confirmed by retrievals based on synthetic data. Realistic retrievals for both total and partial column-averaged CO₂ over Park Falls, Wisconsin on July 12, 15, and August 14, 2004, agree with aircraft measurements. Furthermore, the retrieved total column averages are always underestimated by less than 1%. The results above provide a basis for CO₂ profile retrievals using ground-based observations in the near-infrared region.     

Advanced Catalytic Performance of Au–Pt Double‐Walled Nanotubes and Their Fabrication through Galvanic Replacement Reaction

Bimetallic tubular nanostructures have been the focus of intensive research as they have very interesting potential applications in various fields including catalysis and electronics. In this paper, we demonstrate a facile method for the fabrication of Au–Pt double‐walled nanotubes (Au–Pt DWNTs). The DWNTs are fabricated through the galvanic displacement reaction between Ag nanowires and various metal ions, and the Au–Pt DWNT catalysts exhibit high active catalytic performances toward both methanol electro‐oxidation and 4‐nitrophenol (4‐NP) reduction. First, they have a high electrochemically active surface area of 61.66 m² g^?1, which is close to the value of commercial Pt/C catalysts (64.76 m² g^?1), and the peak current density of Au–Pt DWNTs in methanol oxidation is recorded as 138.25 mA mg^?1, whereas those of Pt nanotubes, Au/Pt nanotubes (simple mixture), and commercial Pt/C are 24.12, 40.95, and120.65 mA mg^?1, respectively. The Au–Pt DWNTs show a markedly enhanced electrocatalytic activity for methanol oxidation compared with the other three catalysts. They also show an excellent catalytic performance in comparison with common Au nanotubes for 4‐nitrophenol (4‐NP) reduction. The attractive performance exhibited by these prepared Au–Pt DWNTs can be attributed to their unique structures, which make them promising candidates as high‐performance catalysts.     

Synthesis,Characterization, and Crystal Structure of Three Coordination Polymers from 5‐(Pyridin‐2‐ylmethyl)aminoisophthalic Acid

Three new complexes: [M(L)(H₂O)] [M = Zn ( 1 ), Co ( 2 ), Ni ( 3 ); H₂L = 5‐(pyridin‐2‐ylmethyl)aminoisophthalic acid] were synthesized under hydrothermal conditions at 180 °C and were characterized by elemental analysis, FT‐IR spectroscopy, single‐crystal X‐ray diffraction, and thermogravimetric analysis (TGA). The results of X‐ray diffraction analysis reveal that complexes 1 – 3 are isostructural and crystallize in the monoclinic system with space group P2₁/c. Each of the complexes displays a (3,3′)‐connected two‐dimensional (2D) wave‐like network with (4,8²) topology, within which five‐membered uncoplanar N,N‐chelated metallacycles are shaped. Delicate N–H ··· O and O–H ··· O hydrogen bonding interactions exist in complexes 1 – 3 . Adjacent 2D layers are linked by intermolecular interactions, resulting in the construction of extended metal‐organic frameworks (MOFs) in complexes 1 and 2 .     

自由面对潜艇尾流场流动特性影响研究

潜艇周围绕流场流动特性会影响潜艇的机动性能, 特别是近水面航行时, 自由面的存在会增大潜艇尾流场的复杂程度.为探究潜艇在近水面航行时自由液面对潜艇尾流场流动特性的影响机理,借助大型水下三维粒子图像测速技术开展潜艇尾流场流动特性研究.首先通过美国泰勒水池标准模型实验结果对试验方法准确性进行验证; 随后,用验证后的模型试验方法对潜艇尾流场进行测量,得到不同潜深工况、不同速度下的桨盘面轴向速度以及脉动速度,同时辅以数值模拟对试验无法测得的兴波波系及中纵剖面速度场加以补充,从兴波角度阐述了自由面对潜艇尾流场流动特性影响机理. 研究结果表明:潜艇在近水面航行时, 随着Fr增大,桨盘面处轴向速度云图中上方等值线整体趋于扁平化, 较4D潜深工况,1.5D潜深工况出现局部脉动速度极大值, 且脉动速度结构整体下移; 自由面存在时,艇体与自由面间流场速度明显增大, 特别在桨盘面区域, 流场速度明显提升.随着Fr增大, 桨盘面处的自由液面高度逐渐降低,这就导致了桨盘面位置出现更大的流体速度, 即造成了桨盘面伴流场挤压现象.      

Analytical solutions for sediment concentration in waves based on linear diffusivity

Two kinds of analytical solutions are derived through Laplace transform for the equation that governs wave-induced suspended sediment concentration with linear sediment diffusivity under two kinds of bottom boundary conditions, namely the reference concentration(Dirichlet) and pickup function(Numann), based on a variable transformation that is worked out to transform the governing equation into a modified Bessel equation. The ability of the two analytical solutions to describe the profiles of suspended sediment concentration is discussed by comparing with different experimental data. And it is demonstrated that the two analytical solutions can well describe the process of wave-induced suspended sediment concentration, including the amplitude and phase and vertical profile of sediment concentration. Furthermore, the solution with boundary condition of pickup function provides better results than that of reference concentration in terms of the phase-dependent variation of concentration.