Investigation of DMAB oxidation at a gold microelectrode in base

A gold microdisk has been used to determine the diffusion coefficient Formula for dimethylamine borane (DMAB) in concentrated alkaline solution. Two steady-state oxidation waves were resolved through the use of microelectrodes. Using the Formula value determined, the coulomb number for both oxidation waves was shown to be 3. The first wave may be further resolved in dilute solutions revealing three one-electron steps. The concentration range wherein the maximum coulombic efficiency for DMAB oxidation on gold may be achieved is demonstrated. An oxidation pathway with a variable coulomb number is suggested

Porous alumina thin films on conductive substrates for templated 1-dimensional nanostructuring

The growth of thin porous anodic aluminum oxide (AAO) films on silicon by anodizing Al on Ti/Au/Si and Ti/Pt/Si substrates in oxalic acid was demonstrated. Removal of the Al2O3 barrier layer was effected by selective chemical etching in H3PO4 and a reversed bias method in the anodizing solution. Ion transport and the influence of the Ti adhesion layer at the oxide–metal interface during the critical stages of anodization and pore opening were investigated. The AAO films may be exploited as templates in the creation of silicon-integrated nanostructured wire arrays. Electrodeposition of Pt into the AAO template yielded a nanowire array with superior methanol oxidation activity that can be integrated in a micro direct methanol fuel cell

Nanoporous gold anode catalyst for direct borohydride fuel cell

This paper reports on the direct electrochemical oxidation of borohydride ions at a nanoporous gold catalyst. The catalyst may be incoroporated as an anode in a Direct Borohydride Fuel Cell (DBFC)

DNA-controlled assembly of protein-modified gold nanocrystals

The controlled assembly in solution of gold nanocrystals modified by attachment of complementary protein-DNA conjugates is described. The size of the aggregates formed can be controlled by the addition of single-stranded DNA, which quickly terminates the assembly process. The rate of formation of the aggregates can also be controlled by varying the salt concentration. Consequently, two distinct regimes of aggregation kinetics are observed. At low salt concentrations, aggregation is shown to be dependent on the rate of duplex formation between the modified gold nanocrystals, i.e., reaction-limited. At higher salt concentrations, aggregation is shown to be dependent only on the rate of diffusion of the nanocrystals, i.e., diffusion-limited. The results presented provide important insights into the rates of formation of nanocrystal assemblies. Moreover, the approach adopted is modular, requiring only the relevant biotin linker chemistry to be developed for a given nanoparticle, while also precluding unfavorable interactions between the DNA and the streptavidin-coated nanoparticle. The ability to control the rate of formation and size of nanocrystal aggregates assembled is important new knowledge. Application of this knowledge will inform future studies of nanocrystal assembly in solution involving different types of nanocrystals, which is of increasing technological significance.This research was supported by a grant from the Petroleum Research Fund (Grant No. PRF# 32879-ACS). The Authors also thank Dr. Hakan Rensmo for helpful discussions and express their gratitude for the services provided by D. Cottell and the staff at the Electron Microscopy Centre, National University of Ireland, Dublin.Peer reviewe

Chemically modified electrodes for recessed microelectrode array

Chemical modifications on recessed microelectrode array, achieved via electrodeposition techniques are reported here. Silicon-based gold microelectrode arrays of 10µm microband and microdisc array were selected and functionalised using sol-gel and nanoporous gold (NPG) respectively. For electrochemically assisted self-assembly (EASA) formati6154on of sol-gel, electrode surface was first pre-treated with a self-assembled partial monolayer of mercaptopropyltrimethoxysilane (MPTMS) before transferring it into the sol containing cetyltrimethyl ammonium bromide (CTAB)/tetraethoxysilane (TEOS):MPTMS (90:10) precursors. A cathodic potential is then applied. It was found that larger current densities were required in ensuring successful film deposition when moving from macro- to micro- dimensions. For NPG modification, a chemical etching process called dealloying was employed. NPG of three different thicknesses have been successfully deposited. All the modified and functionalized microelectrode arrays were characterized by both optical (SEM) and electrochemical analysis (cyclic voltammetry and impedance spectroscopy). An increase in surface area and roughness has been observed and such will benefit for future sensing application

3D interconnection by FIB assisted Pt deposition and electroless nickel deposition on the sides and edges of an I-Seed

This paper reports on the development of a 3D interconnection process leading to the successful assembly of a five-layer 3-D 1mm cube module. This proof of concept module demonstrates the capability for successful integration and interconnection of commercial off the shelf components to fabricate functional modules in 1mm cube dimensions. It also demonstrates that use of established volume scale technologies like Flip-chip, dicing and patterning techniques are viable for fabricating these 1mm modules. The demonstrator consists of LED's bonded to the six sides of the 1mm cube, interconnected and powered up. The work will particularly report on two different processes to fabricate the interconnection pattern using direct Focused Ion Beam (FIB) assisted Pt deposition and electroless metal deposition, which again patterned by FIB. Uniform thickness of the deposit and excellent coverage on all six sides is achieved by electroless nickel deposition. Voltage current characterisation of the deposited Pt shows a resistivity value of 1864 +/- 100 mu Omega cm, whereas electroless Ni film shows a resistivity of 25 mu Omega cm due to boron inclusion. 100 nm An layer is deposited by chemical displacement reaction to enhance the conductivity and solderability of the film

Nanoenabling electrochemical sensors for life sciences applications

Electrochemical sensing systems are advancing into a wide range of new applications, moving from the traditional lab environment into disposable devices and systems, enabling real-time continuous monitoring of complex media. This transition presents numerous challenges ranging from issues such as sensitivity and dynamic range, to autocalibration and antifouling, to enabling multiparameter analyte and biomarker detection from an array of nanosensors within a miniaturized form factor. New materials are required not only to address these challenges, but also to facilitate new manufacturing processes for integrated electrochemical systems. This paper examines the recent advances in the instrumentation, sensor architectures, and sensor materials in the context of developing the next generation of nanoenabled electrochemical sensors for life sciences applications, and identifies the most promising solutions based on selected well established application exemplars

Memorials to the victims of Nazism: the impact on tourists in Berlin

This qualitative study explores tourist responses to memorials to the victims of Nazism in Berlin and the impact they have on the tourist experience. The findings are located in the field of study known as dark tourism, of which visiting memorials is a part. The analysis shows that tourists increased their knowledge of the crimes committed by the Nazis, thus fulfilling the educational function of memorials. Tourists were also overwhelmed by their experience; they attested to feelings of sadness, shock, anger, despair and incomprehension. These feelings made it hard for them to resume the role of tourist after their exposure to a memorial. There was acknowledgement of the extent of commemoration practised in Germany