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1.
Recently the investigation of non-stationary systems exhibiting spatial and dynamic heterogeneities has propelled the development of innovative optical techniques providing the missing link between the scattering and imaging approaches. The novel techniques are characterized by the fact that the scattered radiation is measured close to the sample. They allow to recover information on the structure and dynamics of the system under investigation equivalent to that available with scattering techniques, with the great advantage that they simultaneously allow to achieve a local characterization of the sample, which is lost in traditional scattering measurements. 相似文献
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Netzer NL Qiu C Zhang Y Lin C Zhang L Fong H Jiang C 《Chemical communications (Cambridge, England)》2011,47(34):9606-9608
Highly porous bimetallic nanowires manufactured via a simple galvanic reaction have demonstrated superior activity in surface-enhanced Raman scattering, allowing ultrasensitive chemical detections on isolated porous nanowires in comparison to pristine silver nanowires. 相似文献
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The optical properties of one-dimensional arrays of metal nanoshell dimers are studied systematically using the T-matrix method based on Mie theory, within the context of surface enhanced Raman scattering (SERS). It is shown that the local electromagnetic enhancement can be as high as approximately 4.5 x 10(13) for nanoshell dimer arrays with optimal geometry, and sensitive tunability in the resonant frequency can be gained by varying the geometrical parameters, making such structures appealing templates for SERS measurements with single molecule sensitivity. The extraordinarily high enhancement is attributed to a collective photonic effect constructively superposed onto the intrinsic enhancement associated with an isolated nanoshell dimer. 相似文献
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Lu-Lu Qu Qi-Xia Song Yuan-Ting Li Mao-Pan Peng Da-Wei Li Li-Xia Chen John S. Fossey Yi-Tao Long 《Analytica chimica acta》2013
Au–Ag bimetallic microfluidic, dumbbell-shaped, surface enhanced Raman scattering (SERS) sensors were fabricated on cellulose paper by screen printing. These printed sensors rely on a sample droplet injection zone, and a SERS detection zone at either end of the dumbbell motif, fabricated by printing silver nanoparticles (Ag NPs) and gold nanoparticles (Au NPs) successively with microscale precision. The microfluidic channel was patterned using an insulating ink to connect these two zones and form a hydrophobic circuit. Owing to capillary action of paper in the millimeter-sized channels, the sensor could enable self-filtering of fluids to remove suspended particles within wastewater without pumping. This sensor also allows sensitive SERS detection, due to advantageous combination of the strong surface enhancement of Ag NPs and excellent chemical stability of Au NPs. The SERS performance of the sensors was investigated by employing the probe rhodamine 6G, a limit of detection (LOD) of 1.1 × 10−13 M and an enhancement factor of 8.6 × 106 could be achieved. Moreover, the dumbbell-shaped bimetallic sensors exhibited good stability with SERS performance being maintained over 14 weeks in air, and high reproducibility with less than 15% variation in spot-to-spot SERS intensity. Using these dumbbell-shaped bimetallic sensors, substituted aromatic pollutants in wastewater samples could be quantitatively analyzed, which demonstrated their excellent capability for rapid trace pollutant detection in wastewater samples in the field without pre-separation. 相似文献
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Surface-enhanced Raman scattering (SERS) activity of silver-gold bimetallic nanostructures (a mean diameter of approximately 100 nm) with hollow interiors was checked using p-aminothiophenol (p-ATP) as a probe molecule at both visible light (514.5 nm) and near-infrared (1064 nm) excitation. Evident Raman peaks of p-ATP were clearly observed, indicating the enhancement Raman scattering activity of the hollow nanostructure to p-ATP. The enhancement factors (EF) at the hollow nanostructures were obtained to be as large as (0.8+/-0.3)x10(6) and (2.7+/-0.5)x10(8) for 7a and 19b (b(2)) vibration mode, respectively, which was 30-40 times larger than that at silver nanoparticles with solid interiors at 514.5 nm excitation. EF values were also obtained at 1064 nm excitation for 7a and b(2)-type vibration mode, which were estimated to be as large as (1.0+/-0.3)x10(6) and (0.9+/-0.2)x10(7), respectively. The additional EF values by a factor of approximately 10 for b(2)-type band were assumed to be due to the chemical effect. Large electromagnetic EF values were presumed to derive from a strong localized plasmas electromagnetic field existed at the hollow nanostructures. SERS activity of hollow nanostructures with another size (a mean diameter of approximately 80 nm) was also investigated and large EF for 7a and b(2)-type band are obtained to be (0.6+/-0.3)x10(6) and (1.7+/-0.7)x10(8), respectively, at 514.5 nm excitation and (0.2+/-0.1)x10(6) and (0.6+/-0.2)x10(7), respectively, at 1064 nm excitation. Although the optical properties of the hollow nanostructures have not yet been well studied, high SERS activities of the nanostructures with hollow interiors have been exhibited in our report. 相似文献
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Novel silver-gold bimetallic nanostructures were prepared by seeding with silver nanoplates in the absence of any surfactants. During the synthesis process, it was found that the frameworks of silver nanoplates were normally kept though the basal plane of silver nanoplates became rugged. The real morphology of these nanostructures depended on the molar ratio of gold ions to the seed particles. When the molar ratio of gold ions to silver atoms increased from 0.5 to 4, porous or branched silver-gold bimetallic nanostructures could be made. The growth mechanism was qualitatively discussed based on template-engaged replacement reactions and seed-mediated deposition reactions. Due to the unusual structures, they exhibited interesting optical properties. Moreover, they were shown to be an active substrate for surface-enhanced Raman scattering measurements. 相似文献
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LIU Zhongxin SONG Hongwei YU Lixin YANG Linmei & PAN Guohui . Key Laboratory of Excited State Physics Changchun Institute of Optics Fine Mechanics Physics Chinese Academy of Sciences Changchun China . Graduate School of the Chinese Academy of Sciences Beijing China 《中国科学B辑(英文版)》2005,48(5):431-435
Noble metal nanostructures have been the research focus for many decades because of their real or poten-tial applications, such as catalysis, photography, optics, electronics, optoelectronics, information storage, bio-logical and chemical sensing, surface… 相似文献
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Ariafard A Hyland CJ Canty AJ Sharma M Brookes NJ Yates BF 《Inorganic chemistry》2010,49(23):11249-11253
Ligand effects in bimetallic high oxidation state systems containing a X-Pd-Pd-Y framework have been explored with density functional theory (DFT). The ligand X has a strong effect on the dissociation reaction of Y to form [X-Pd-Pd](+) + Y(-). In the model system examined where Y is a weak σ-donor ligand and a good leaving group, we find that dissociation of Y is facilitated by greater σ-donor character of X relative to Y. We find that there is a linear correlation of the Pd-Y and Pd-Pd bond lengths with Pd-Y bond dissociation energy, and with the σ-donating ability of X. These results can be explained by the observation that the Pd d(z(2)) population in the PdY fragment increases as the donor ability of X increases. In these systems, the Pd(III)-Pd(III) arrangement is favored when X is a weak σ-donor ligand, while the Pd(IV)-Pd(II) arrangement is favored when X is a strong σ-donor ligand. Finally, we demonstrate that ligand exchange to form a bimetallic cationic species in which each Pd is six-coordinate should be feasible in a high polarity solvent. 相似文献
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Jean-Luc Fillaut Neerja Nagpal Dua Loïc Toupet 《Journal of organometallic chemistry》2006,691(26):5610-5618
Wire like mono- and poly-nuclear molecules based on alkynyl ruthenium complexes whose core unit is trans-[Ru(CC-R)(R′CN)(dppe)2][PF6] are readily formed in soft conditions. The electronic dual character of the metallic unit, donor through the acetylide moiety, acceptor versus the nitrile ligand is exemplified through electrochemical studies of a series of ethynylferrocene and cyanoferrocene derivatives. A single crystal X-ray diffraction analysis of the [(dppe)2(PhCC)Ru(NC-C6H4-CN)Ru(CCPh)(dppe)2][2PF6] bimetallic complex 5 shows that the global structure of such complexes consists of wire type dimetallic units. With the availability of this versatile, direct, and simple route, a new class of extended rigid rod systems of nanometric size with multilevel electron transfers is readily accessed. 相似文献
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More than 85% of 10 mg L(-1) of pentachlorophenol (PCP) was removed by magnesium/silver (206/1.47 mM) bimetal system in the presence of acetic acid. Dechlorination was found to be sequential and phenol was identified as the ultimate hydrocarbon skeleton along with some accumulation of tetra-, tri-, and dichlorophenols. The dechlorination reaction was found to follow second-order kinetics. Lower PCP removal efficiency (35%) was observed when the reaction was carried out in the absence of acid using Mg(0)/Ag system. When the reaction was conducted using Mg(0) alone in the presence of acid, substantial sorption of PCP occurred with very low efficiency of PCP dechlorination. Dechlorination studies on 10 mg L(-1) initial concentrations of 2,3,4,6-tetrachlorophenol (2,3,4,6-TeCP) and 2,4,5-trichlorophenol (2,4,5-TCP), under identical conditions as to PCP, revealed that dechlorination efficiency and reaction rate constants decrease with decreasing number of chlorine atoms on the target compound. A correlation (R(2)>0.9) between the dechlorination rate constants and E(LUMO) for chlorophenols was obtained. 相似文献
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Jeffrey T. Koberstein 《Journal of Polymer Science.Polymer Physics》1982,20(4):593-602
A small-angle neutron scattering method is presented for the determination of single-chain scattering functions in heterogeneous two-phase polymeric materials such as incompatible polymer blends and microphase-separated diblock copolymers. Development of the method makes use of both the discrete and continuum approaches to scattering theory. In this fashion it is shown that extraction of the single-chain scattering function requires only two experimental observations, regardless of the compressibility of the system. These experiments consist of small-angle neutron scattering profiles from two samples: an unlabeled two-phase material and a similar two-phase material in which a portion of the molecules in one phase have been replaced by molecules which are contrast labeled by isotopic deuterium substitution. Anticipated difficulties associated with actual application of the procedure and requirements of the necessary experimental samples are discussed. 相似文献
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Millán A Campaña AG Bazdi B Miguel D de Cienfuegos LA Echavarren AM Cuerva JM 《Chemistry (Weinheim an der Bergstrasse, Germany)》2011,17(14):3985-3994
The allylation, crotylation and prenylation of aldehydes and ketones with stable and easily handled allylic carbonates is promoted by a Ti/Pd catalytic system. This Ti/Pd bimetallic system is especially convenient for the allylation of ketones, which are infrequent substrates in other related protocols, and can be carried out intramolecularly to yield five- and six-membered cyclic products with good stereoselectivities. In addition, Ti/Pd-mediated reductions and Würtz-type dimerisation reactions can be readily carried out from allyl carbonates and carboxylates. 相似文献
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Interpretation of light scattering from supermolecular structures in liquid systems by master curves
By a detailed analysis of light scattering curves, a more complete characterization of colloidal particles may be achieved. For this purpose, a fitting procedure based on theoretical master curves of models of polydisperse systems of homogeneous spheres and Gaussian coils is presented. The use of a suitable logarithmic distribution function makes it possible to separate the influence of polydispersity from that of particle size on the shape of the scattering curve. A double logarithmic plot of master curves reduces the fitting procedure to translations of the experimental curves. The reliability and accuracy of this procedure are demonstrated by light scattering results on solutions of a polyelectrolyte complex with variation of salt content. 相似文献
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Tomsic M Bester-Rogac M Jamnik A Kunz W Touraud D Bergmann A Glatter O 《Journal of colloid and interface science》2006,294(1):194-211
Structural properties of ternary systems composed of nonionic surfactant dodecyl-poly(ethylene oxide-23) ether (C12E23, commercial name: Brij 35), water and various alcohols from ethanol to 1-decanol have been investigated using small-angle X-ray scattering (SAXS) and dynamic light scattering (DLS) techniques. All measurements were performed at the temperature 25 degrees C. SAXS experimental data were put on absolute scale using water as a secondary standard. The data of water-rich mixtures at low to moderate surfactant concentrations were evaluated using the generalized indirect Fourier transformation method (GIFT), which is based on the simultaneous determination of the intra- and inter-particle scattering contributions. In this way, the size and the shape of interacting scattering particles in real space could be deduced. The systems with a relatively low surfactant concentration (5 mass%) were studied most extensively. In these cases, the water-rich regions of the phase diagrams could be investigated into more detail, since in the alcohol-rich regions problems with the GIFT evaluation of the SAXS data were encountered. The presented results demonstrate the level of structural details that can be obtained on the basis of scattering methods and point out the specific stages of data evaluation and interpretation where one must be extremely precautious. As such they reveal the inner structuration of the complex ternary systems of our present interest. In parallel, they also indicate that the longer chain alcohols actually behave as real oil phases in the studied systems, as one might expect, and also confirm the well-known properties of different short to medium chain alcohols that act as co-solvents and/or co-surfactants in microemulsion systems depending on their chain length. 相似文献
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纳米催化介于均相催化与多相催化之间, 也称为”半多相催化”, 目前正受到人们越来越多的关注. 最近几年, 应用双金属纳米材料进行催化研究取得了很大进展, 使用这些催化材料可以增加反应活性和选择性, 而且能很好地得以回收. 本文综述了双金属纳米材料催化的各种有机反应, 如选择性氧化/氢化、偶联和其它反应(脱卤、酰胺化、还原氨化、芳基硼酸与烯酮的1,4-不对称加成和氢解). 将双金属纳米材料用于催化合成更加复杂的有机分子值得期待. 在双金属纳米有机催化领域, 基础理论和实际应用尚有较大的发展空间. 未来该领域的发展需要开展多学科的合作, 包括合理设计和可控制备相关的双金属纳米材料、深入理解催化机理及发展计算催化. 相似文献
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Small angle neutron scattering is a powerful, non-destructive technique that can provide both structural and compositional information. Recently, it has been applied to the field of battery research and has helped elucidate some of the phenomena that are traditionally difficult to probe, including lithiation mechanisms, solid electrolyte interface formation/composition, and electrode microstructure. Specific components of interest can be selectively probed through the application of targeted experiments, contrast variation, and specific composition/structural models gained from complementary data from other analytical techniques. 相似文献