Preparation, structure, and optical properties of nanoporous gold thin films

Thin nanoporous gold (np-Au) films, ranging in thickness from approximately 40 to 1600 nm, have been prepared by selective chemical etching of Ag from Ag/Au alloy films supported on planar substrates. A combination of scanning electron microscopy (SEM) imaging, synchrotron grazing incidence small angle X-ray scattering, and N2 adsorption surface area measurements shows the films to exhibit a porous structure with intertwined gold fibrils exhibiting a spectrum of feature sizes and spacings ranging from several to hundreds of nanometers. Spectroscopic ellipsometry measurements (300-800 nm) reveal the onset of surface plasmon types of features with increase of film thicknesses into the approximately 200 nm film thickness range. Raman scattering measurements for films functionalized with a self-assembled monolayer formed from 4-fluorobenzenethiol show significant enhancements which vary sharply with film thickness and etching times. The maximum enhancement factors reach approximately 10(4) for 632.8 nm excitation, peak sharply in the approximately 200 nm thickness range for films prepared at optimum etching times, and show high spot to spot reproducibility with approximately 1 microm laser spot sizes, an indication that these films could be useful as durable, highly reproducible surface-enhanced Raman substrates.     

Isotachophoretic purification of nanoparticles: tuning optical properties of quantum dots

Synthesized nanoparticles often require fine fractionation according to shape, dimension, mass, chemical composition, charge, and other properties in order to become suitable for practical use. Quantum dots (QDs) are luminescent nanocrystals with narrow emission peaks. This property has been widely utilized for the multiplexed sensing and barcoding of microparticles. QDs with narrower emission peaks are preferred for such applications. The width of the emission peaks can be significantly reduced after purification. A newly developed preparative isotachophoretic method employs the dependence of spectral properties and electrophoretic mobility on the diameter of QDs. Separated fractions of QDs revealed narrower emission peaks (72% of the original width) and improved quantum yield (two-fold). The usefulness of the developed isotachophoresis for purification and analysis of other nanostructures, for example, plasmonic nanoparticles and nanobioconjugates, is expected, too.     

Concept of optical channel as a guide for tuning the optical properties of insulating materials

The utility of the concept of optical channel in understanding the optical properties of insulating materials was briefly reviewed by considering how the indices of refraction n of the seven TiO₂ allotropes, TiOF₂, TiF₄ and the binary compounds MQ (M = Zn, Cd; Q = O, S, Se, Te) are related to their total absorption power per formula unit I(ɛ₂) × V and their formula unit volume V. Important factors governing the optical properties of insulating materials are discussed.     

Luminescence tuning and enhanced nonlinear optical properties of nanocomposites of ZnO-TiO2

In this article we present the spectral and nonlinear optical properties of ZnO-TiO(2) nanocomposites prepared by colloidal chemical synthesis. Emission peaks of ZnO-TiO(2) nanocomposites change from 340 nm to 385 nm almost in proportion to changes in E(g). The nanocomposites show self-defocusing nonlinearity and good nonlinear absorption behaviour. The nonlinear refractive index and the nonlinear absorption increase with increasing TiO(2) volume fraction at 532 nm and can be attributed to the enhancement of exciton oscillator strength. ZnO-TiO(2) is a potential nanocomposite material for the tunable light emission and for the development of nonlinear optical devices with a relatively small limiting threshold.     

Alloyed semiconductor quantum dots: tuning the optical properties without changing the particle size

Alloyed semiconductor quantum dots (cadmium selenium telluride) with both homogeneous and gradient internal structures have been prepared to achieve continuous tuning of the optical properties without changing the particle size. Our results demonstrate that composition and internal structure are two important parameters that can be used to tune the optical and electronic properties of multicomponent, alloyed quantum dots. A surprising finding is a nonlinear relationship between the composition and the absorption/emission energies, leading to new properties not obtainable from the parent binary systems. With red-shifted light emission up to 850 nm and quantum yields up to 60%, this new class of alloyed quantum dots opens new possibilities in band gap engineering and in developing near-infrared fluorescent probes for in vivo molecular imaging and biomarker detection.     

Enhanced electrochromic properties of self-organized nanoporous WO3

Self-organized nanoporous layers of WO₃ were grown by anodization, and their electrochemical and electrochromic properties were investigated and compared to compact anodic layers. As-formed WO₃ layers had an amorphous structure but could be transferred to a monoclinic structure by thermal annealing treatment. Compared to the compact layer, the nanoporous WO₃ layer showed strongly enhanced ion intercalation capacity with reversible characteristics during electrochemical cycling processes. The nanoporous structures showed a significantly enhanced electrochromic contrast, faster switching response, and less sensitivity to intercalation loss by crystallization.     

A simple solvothermal route towards the morphological control of ZnO and tuning of its optical and photocatalytic properties

ZnO nanoparticles with different morphologies were solvothermally synthesized by controlling the alkali (sodium hydroxide) concentration in an isopropanol solution. The products were characterized by means of powder X-ray diffraction, UV-visible absorption spectra, scanning electron microscopy, transmission electron microscopy, and selected area electron diffraction. The morphologies of the formed ZnO nanocrystals were dependent on the concentration of the alkali, and with increases of sodium hydroxide concentration, the ZnO nanocrystals evolved from rod to hexagonal bipyramid, and then to a flower-like nanostructure. The flower-like nanostructure resulted from the etching of the hexagonal bipyramid by the excess alkali. The photoluminescence and photocatalytic properties of the prepared ZnO were investigated. The difference of green emission among the ZnO nanocrystals indicated that a higher sodium hydroxide concentration led to a higher level of defects. The size, the surface structure and defects in the ZnO nanocrystals affected its photo-degradation characteristics.     

From 1D chain to 3D network: tuning hybrid II-VI nanostructures and their optical properties

In an effort to make semiconductor nanomaterials with tunable properties, we have deliberately designed and synthesized a family of novel organic-inorganic hybrid nanocomposites based on II-VI semiconductors with structures ranging from one-dimensional (1-D) chain to two-dimensional layer (2-D) to three-dimensional (3-D) framework. All nanostructures exhibit strong quantum confinement effect (QCE), while possessing a perfectly periodic arrangement. The optical absorption experiments show that all compounds generate a very large blue shift in the absorption edge (1.0-2.0 eV) due to the strong QCE. More significantly, their band edge shift and optical properties can be tuned by changing the dimensionality of inorganic motifs as well as overall crystal structures. Raman studies reveal that not only do these structures have distinctly different vibrational signatures from those of the II-VI host semiconductors, but they also differ significantly from each other as a result of changes in dimensionality. The crystal structures of these nanocomposite materials have been characterized by single crystal and/or powder X-ray diffraction methods. [ZnTe(pda)] (1; pda = propanediamine) is composed of 1-D chains of [ZnTe] with pda chelating to Zn atoms. [ZnTe(N(2)H(4))] (2; N(2)H(4) = hydrazine) and [ZnTe(ma)] (3; ma = MeNH(2) = methylamine) are two-dimensional (2-D) layered structures containing [ZnTe] slabs and terminal hydrazine (2) or methylamine (3) molecules. The crystal structures of [CdSe(en)(0.5)] (4; en = ethylenediamine) and [CdSe(pda)(0.5)] (5) are 3-D networks containing [CdSe] slabs bridged by bidentate organic diamine molecules. Crystal data for 1: Orthorhombic, space group Pbcm, a = 9.997(2), b = 6.997(1), c = 10.332(2) A, Z = 4. For 2: Monoclinic, space group P2(1), a = 4.2222(6), b = 6.9057(9), c = 7.3031(10) A, beta = 98.92(8) degrees, Z = 2. For 3: Orthorhombic, Pbca, a = 7.179(1), b = 6.946(1), c = 18.913(4) A, Z = 8. For 4: Orthorhombic, Pbca, a = 7.0949(3), b = 6.795(3), c = 16.7212(8) A, Z = 8. For 5: Orthorhombic, Cmc2(1), a = 20.6660(12), b = 6.8900(4), c = 6.7513(4) A, Z = 8.     

Advanced functional properties in nanoporous coordination framework materials

Coordination framework materials display a rich array of host-guest properties and are notable amongst porous media for their extreme chemical versatility. This article highlights a number of areas where specific function has been incorporated into these framework host lattices.     

Controlling optical properties and interchain interactions in semiconducting polymers by encapsulation in periodic nanoporous silicas with different pore sizes

The photophysics of MEH-PPV incorporated into the pores of periodic silica hosts has been investigated in an effort to understand the role played by interchain aggregation and chain morphology in polaron production. In this work, guest/host interactions were used to incorporate MEH-PPV into the straight, homogeneous pores of hexagonal surfactant- or polymer-templated mesoporous silicas of varying pore diameters. Polarized photoluminescence and photoluminescence excitation spectroscopy were then used to investigate the polymers' environment within the silica pores. Experiments exploiting luminescence peak shifts and depolarization indicate that depending on the pore size and preparation conditions, the alignment and packing of the polymer chains within the pores could be controlled. Samples could be produced with isolated chains, interacting straight chains, and coiled interacting chains. The sub-bandgap absorption by polarons was then measured with photoinduced absorption as a function of pore size. Small-diameter pores that allowed single polymer chains to reside within the pore showed little evidence of interchain contact and had a low polaron yield. Increasing the number of polymer chains within the pore increased the polaron yield. Finally, when the pores were large enough that the chains could coil, strong polaron absorption was observed, indicative of a further increase in polaron yield or an increase in polaron lifetime. The polaron absorption spectra also sharpen and red shift with increasing pore diameter, suggesting that excitons may migrate to lower energy polymer segments in samples where polymer chains are both coiled and interacting.     

The role of water in the epoxidation over gold-titania catalysts

Water is capable of reducing the rate of deactivation of gold-titania catalysts for propene epoxidation.     

Correlation of structural and permeation properties in sol-gel-made nanoporous membranes

The aim of the present work was to establish a fundamental link between the basic structural properties of ceramic nanoporous membranes made by the sol-gel process and their respective transport properties, for a systematic evaluation of their performance in gas and liquid applications. For this purpose, supported and unsupported gamma-Al2O3 and TiO2 membranes were prepared from different colloidal dispersions (sols) by a sol-gel dipping process followed by drying and calcination, resulting in structures of crystallites of different shape and stacking arrangement. Accordingly, the pore structure of each membrane was simulated employing process-based reconstruction techniques and the permeation properties were predicted by solving the appropriate transport equations in the generated structures. Excellent agreement was achieved between the computed and experimental permeability values in the Knudsen and viscous flow regimes, validating the considerations made regarding the basic structural characteristics and the procedure for generation of the membrane structures. Moreover, it was shown that the shape and stacking arrangement of the primary particles (crystallites) of the sol have a major impact on the formation of pathways in the membrane pore structures and control the transport and therefore also the separation properties of these materials.     

Preparation and thermal properties of chemically prepared nanoporous silica aerogels

This work focuses on the dependence preparation conditions—structure—physical properties of hydrophobic silica aerogels, all of them prepared under subcritical drying conditions (70 °C and 0.4 atm.), thus aiming at potential application as case insulation filling in heat pumps. The so prepared, millimeter scaled nano-porous hydrophobic silica aerogel granules were analyzed with standard electron microscope and atomic force microscopy, IR spectroscopy, UV/Vis spectroscopy, differential scanning calorimetry and thermal conductivity measurements. The physical properties of the aerogels were compared with commercial aerogel granules. A method for contact angle measurement of micro-droplets situated on the silica granules was proposed to quantify the level of their hydrophobicity.     

Electrochemical properties of nanoporous carbon electrodes in various nonaqueous electrolytes

Electrical double layer and electrochemical characteristics at the nanoporous carbon|acetonitrile interface with additions of Et₄NBF₄, Et₃MeNBF₄, EtMe₃NBF₄, LiClO₄, and LiBF₄ have been studied by cyclic voltammetry and impedance spectroscopy methods. A value of zero charge potential, dependent on the structure of the cations as well as on the composition of the anions, the region of ideal polarizability, and other characteristics has been established. Analysis of the complex plane plots shows that the nanoporous carbon|acetonitrile+0.1 M electrolyte (Et₄NBF₄, Et₃MeNBF₄, or EtMe₃NBF₄) interface can be simulated by the equivalent circuit, in which the two parallel conduction parts in the solid and liquid phases are interconnected by the double layer capacitance in parallel with the complex admittance of the hindered reaction of the charge transfer process or of the partial charge transfer (i.e. adsorption stage limited) process. The values of the characteristic frequency depend on the electrolyte composition and on the electrode potential, i.e. on the nature of the ions adsorbed at the surface of the nanoporous carbon electrode. In the region of moderate a.c. frequencies, the modified Randles-like equivalent circuit has been used for simulation of the complex plane plots. In the region of negative surface charge densities, the intercalation process of Li⁺ ions from LiClO₄ and LiBF₄ solutions into the surface film is possible and these data can be simulated using the modified Ho et al. model or Meyer et al. model. Electronic Publication     

Diffusion properties of dye molecules in nanoporous TiO2 networks

The adsorption of ruthenium-dye molecules out of ethanol solution onto TiO2 particles of nanoporous TiO2 films was used to study the molecules' diffusion through these layers by means of optical absorption spectrometry. Dependent on pore size, porosity, and particle size, effective diffusion constants as low as D(eff) = 4 x 10(-9) cm2/s were deduced from the uptake curves by applying a simple model for combined diffusion and adsorption. These diffusion constants for diffusion through the nanoporous network are up to 3 orders of magnitude lower than in bulk ethanol and are discussed with respect to the properties of the nanoporous material.     

Fabrication and electrochemical properties of novel nanoporous platinum network electrodes

Three-dimensional nanoporous Pt networks with a high surface area were directly grown on titanium substrates through a simple hydrothermal-assisted seed growth method.     

Electric transport properties of ultra-and nanoporous glasses in electrolyte solutions

Electric transport characteristics (conductivity, specific surface conductance, and transport numbers of counterions) for nano-and ultraporous glass membranes with pore radii of 1.3–160 nm are studied and compared for chloride solutions containing single-, double-, and triple-charged cations.     

Pi-interaction tuning of the active site properties of metalloproteins

The influence of pi-interactions with a His ligand have been investigated in a family of copper-containing redox metalloproteins. The Met16Phe and Met16Trp pseudoazurin, and Leu12Phe spinach and Leu14Phe Phormidium laminosum plastocyanin variants possess active-site pi-contacts between the introduced residue and His81 and His87/92 respectively. The striking overlap of the side chain of Phe16 in the Met16Phe variant and that of Met16 in wild type pseudoazurin identifies that this position provides an important second coordination sphere interaction in both cases. His-ligand protonation and dissociation from Cu(I) occurs in the wild type proteins resulting in diminished redox activity, providing a [H(+)]-driven switch for regulating electron transfer. The introduced pi-interaction has opposing effects on the pKa for the His ligand in pseudoazurin and plastocyanin due to subtle differences in the pi-contact, stabilizing the coordinated form of pseudoazurin whereas in plastocyanin protonation and dissociation is favored. Replacement of Pro36, a residue that has been suggested to facilitate structural changes upon His ligand protonation, with a Gly, has little effect on the pKa of His87 in spinach plastocyanin. The mutations at Met16 have a significant influence on the reduction potential of pseudoazurin. Electron self-exchange is enhanced, whereas association with the physiological partner, nitrite reductase, is only affected by the Met16Phe mutation, but kcat is halved in both the Met16Phe and Met16Trp variants. Protonation of the His ligand is the feature most affected by the introduction of a pi-interaction.     

Thiadiazoloquinoxalines: tuning physical properties through smart synthesis

The synthesis of π-conjugated acceptors based on thiadiazoloquinoxaline (TQ) derivatives is described. Apart from reporting on the functionalization of the TQ core, the influence of the substituents was studied by UV-vis absorption and emission spectroscopy, cyclic voltammetry measurements, and DFT calculations. By changing the donor as well as the π-spacer, a fine-tuning of the photo- and electrochemical properties was achieved.