Nanostructured gold surfaces as reproducible substrates for surface‐enhanced Raman spectroscopy

Raman spectroscopy is a common tool for the qualitative and quantitative chemical analysis of molecules. Although the unique identification of molecules is possible via their vibrational lines, high concentrations (mmol/l) are needed for their nonresonant excitation owing to their low scattering cross section. The intensity of the Raman spectra is amplified by the use of the surface‐enhanced Raman scattering (SERS) technique. While the use of silver sols results only in a limited reproducibility of the Raman line intensities, lithographically designed, nanostructured gold surfaces used as SERS‐active substrates should, in principle, combine the high sensitivity with better reproducibility. For this purpose, we have produced gratings of gold dots on Si(001) surfaces by means of electron beam lithography. Qualitative and quantitative investigations of crystal violet (CV) performed using nanostructured surfaces give high reproducibility and enhancement of the Raman lines. The substrates are reusable after cleaning; all results presented could be obtained from a single SERS substrate. For the experiments very low laser powers were used. Copyright © 2006 John Wiley & Sons, Ltd.     

Self-assembled all-inclusive organic-inorganic nanoparticles enable cascade reaction for the detection of glucose

Traditional colorimetric glucose biosensor generally involves complex assay procedures. Free labile enzymes and peroxidase substrates are used separately for triggering a chromogenic reaction. These limits result in inferior enzyme stability and defective enzymatic catalytic efficiency, making it hard to routinely utilize them for the direct and fast test of glucose. In this work, we provide an all-inclusive substrates/enzymes nanoparticle employed 3,3′5,5′-tetramethylbenzidine (TMB) as chromogenic substrates and glucose oxidase (GOx)/horseradish peroxidase (HRP) as signal amplifier enzymes (TMB-GH NPs) by the molecule self-assembly technique. The “all-inclusive” nanoparticles can realize the tandem colorimetric reactions, and the oxidation product of TMB (ox-TMB) exhibits a strong NIR laser-driven photothermal effect, thus allowing quantitative photothermal detection of glucose. Owing to the restriction of the molecular motion of GOx, HRP, and TMB, the distance of mass transfer between substrates was shortened largely, leading to improved catalytic activity for glucose. Overall, our strategy will simplify the analysis procedure, furthermore, these integrated nanoparticles not only display higher stability and activity than that of the free GOx/HRP system and possesses an excellent performance for colorimetric and photothermal bioassay of glucose simultaneously. We believe that this unique technique will give good inspirations to develop simple and precise methods for bioassay.     

Fabrication and characterization of Ti-Ba-Ca-Cu-O superconducting films on LaAlO3 substrates

A multi-step process is used to fabricate Tl₂Ba₂Ca₁Cu₂O₈ films on (100) LaA10₃ substrates. Submicron thick precursor films of Ba-Ca-Cu-O are rf magnetron sputter deposited from a single target. Film stoichiometry is measured by ion beam backscattering spectroscopy. Deficiencies of the alkaline earths that are found in the precursor films are then compensated for by the addition of appropriate CaF₂ and/or BaF₂ films onto the surface of the precursor film. Post deposition annealing of the films is then done in an atmosphere of thallium oxide and oxygen in order to form the superconducting phases. The annealed films are examined using x-ray diffraction (XRD), an ac inductance technique, and critical current in an external magnetic field. XRD shows the c-axis length of the superconducting phase to increase as the overall film stoichiometry approaches 2212. The transition widths measured by inductive coupling weakly correlate with 77 K critical current measurements. Our best critical current results are 1.5*10⁶ amps/ cm² for a film measured at 4 K in an 8 T magnetic field (parallel to the films' c-axis).     

Structure-Chemical Analysis of Multiple Complexations by Cyclodextrins

The interactions between cyclodextrin and substrates having two binding sites in aqueous solution are reviewed. For such substrates, multiple equilibria, NMR chemical shift variations with full binding, solution structures of complexes, and the effect of cavity size are analyzed quantitatively. After general treatments of multiple equilibria and chemical shifts are given, they are applied to three bivalent substrates of diheptanoyllecithin, dialkyldimethylammonium bromide, and oxyphenium bromide for demonstrating their usefulness. The solution structures of complexes play a crucial role in these basic researches as well as the applications of cyclodextrins, such as bitter taste reduction and stabilization of labile substrates.     

Excimer laser ablation of thin titanium oxide films on glass

Thin titanium dioxide films are deposited on glass substrates by magnetron sputter deposition. They are irradiated in air, by means of a KrF excimer laser. The ablation rate is measured as a function of the laser fluence per pulse, F, and of the number of pulses, N. Above a fluence threshold, the films are partially ablated. The ablated thickness does not vary linearly with N. This is the signature of a negative feedback between the film thickness and the ablation rate. The origin of this negative feedback is shown to be due to either thermal or electronic effects, or both. At high F, the film detachs from the substrate.     

A new buffer layer for MOCVD growth of GaN on sapphire

High quality GaN films have been grown on sapphire substrates (C face and A face) by atmospheric pressure metalorganic chemical vapor deposition (MOCVD) using a new buffer layer. With our reactor configuration and growth parameters, a GaN film grown on a single GaN buffer layer appears opaque with high density of hexagonal pits. Using a single A1N buffer layer results in extremely nonuniform morphology with mirror-like areas near the edge of the substrates and opaque areas in the center. The double buffer layer we report here, with GaN as the first layer and A1N as the second, each with an optimized thickness, leads to mirror-like films across the entire substrate. Scanning electron microscopy, photoluminescence, x-ray diffraction, and van der Pauw geometry Hall measurement data are presented to establish the quality of our films. The mechanism for this new buffer layer is also discussed.     

Detecting enzymes in living cells using fluorogenic substrates

Characteristics of fluorogenic substrates designed for detection of enzyme activity in living cells are reviewed. Improved retention of the fluorescent products in the cell of origin can be achieved by structural modifications to the substrate that result in association with membrane lipids or conjugation to intracellular glutathione. Newly-developed substrates that yield fluorescent precipitates provide the additional advantage of allowing subcellular localization of sites of enzymatic activity. Improved detection sensitivity can also be achieved by targeted delivery of substrates for processing by specific organelles. Substrates designed for monitoring oxidative activity and lipid metabolism provide examples of this approach.     

提高发光二极管(LED)外量子效率的途径

发光二极管的内量子效率与外量子效率之间存在巨大的差距,主要介绍了提高发光二极管(LED)外量子效率的几种途径,包括生长分布布喇格反射层(DBR)技术,将射向衬底的光反射回表面;制作透明衬底(TS)取代原有的GaAs衬底;改变LED几何外形来缩短光在LED内部反射的路程以及限制全反射现象的表面粗化技术。对比了每种方法的发展过程及效率。     

Polymer brushes on hydrogen-terminated silicon substrates via stable Si—C bond

A universal and straightforward method for the preparation of polymer brushes via the formation of Si-C bond on silicon substrates through the UV-induced photopolymerization is demonstrated.     

Advanced Engineering for Cathode in Lithium–Oxygen Batteries: Flexible 3D Hierarchical Porous Architecture Design and Its Functional Modification

Modern technology constantly requires smaller, more efficient lithium–oxygen batteries (LOBs). To meet this need, a chemical vapor deposition (CVD) method is used to create an innovative cathode design with both a hierarchical porous nanostructure and a 3D flexible macroscopical morphology. This method employs architectural optimization to further improve cathodic ORR and OER performance via heteroatom doping, surface-sprouted carbon nanofibers (CNFs) grafting, and boundary exposing. The cathode consists of a 3D hierarchical porous graphene foam (PGF), along with RuO₂ nanoparticles impregnated and nitrogen doped CNFs (RuO₂@NCNFs), where the PGF serves as a structural support and cathodic current collector, and the RuO₂@NCNFs work as a superior bi-functional catalyst. The cathode delivers an outstanding discharge capacity of 8440 mAh g_cathode⁻¹ while maintaining a recharge plateau at ≈4.0 V, and can cycle for over 700 rounds without obvious degeneration under a fixed capacity. Notably, this free-standing cathode can be directly used in LOBs without the need for additional substrates or current collectors. Therefore, the current densities and capacities herein are calculated based on the total weight of the cathodes. These results demonstrate the RuO₂@NCNFs-PGF cathode's remarkable potential for LOB applications, and this rational cathodic structure may be extended to other highly efficient catalyst applications.