Breakdown of Atomic-Sized Metallic Contacts Measured on Nanosecond Scale

We report on a study of atomic-sized metallic contacts on a time scale of nanoseconds using a combined DC and AC circuit. The approach leads to a time resolution 3−4 orders of magnitude faster than the measurements carried out to date, making it possible to observe fast transient conductance-switching events associated with the breakdown, re-formation, and atomic scale structural rearrangements of the contact. The study bridges the wide gap in the time scales between the molecular dynamic simulations and real world experiments, and the method may be applied to study nano- and subnanosecond processes in other nanoscale devices, such as molecular junctions

Ionic Screening of Charged-Impurity Scattering in Graphene

We have studied the ionic screening effect on the charge transport properties of graphene field effect transistors. By increasing the ionic concentration, we found dramatic increases in the carrier mobilities and systematic changes in the position and magnitude of minimum conductivity, as well as the width of minimum conductivity plateau, which supports the theory of long-range Coulomb scattering. We also observed clear conductivity saturation and systematic crossover from the linear to constant conductivity regimes

Single Molecule Conductance, Thermopower, and Transition Voltage

We have measured the thermopower as well as other important charge transport quantities, including conductance, current–voltage characteristics, and transition voltage of single molecules. The thermopower has little correlation with the conductance, but it decreases with the transition voltage, which is consistent with a theory based on Landauer’s formula. Since the transition voltage reflects the molecular energy level alignment, our finding also shows that the thermopower provides valuable information about the relative alignment between the molecular energy levels and the electrodes’ Fermi energy level

Electron−Phonon Interactions in Single Octanedithiol Molecular Junctions

We study the charge transport properties and electron−phonon interactions in single molecule junctions, each consisting of an octanedithiol molecule covalently bound to two electrodes. Conductance measurements over a wide temperature range establish tunneling as the dominant charge transport process. Inelastic electron tunneling spectroscopy performed on individual molecular junctions provides a chemical signature of the molecule and allows electron−phonon interaction induced changes in the conductance to be explored. By fitting the conductance changes in the molecular junction using a simple model for inelastic transport, it is possible to estimate the phonon damping rates in the molecule. Finally, changes in the inelastic spectra are examined in relation to conductance switching events in the junction to demonstrate how changes in the configuration of the molecule or contact geometry can affect the conductance of the molecular junction

Chemical Sensor Based on Microfabricated Wristwatch Tuning Forks

We report here a chemical sensor based on detecting the mechanical response of a thin (∼10-μm) polymer wire stretched across the two prongs of a wristwatch quartz tuning fork (QTF). When the fork is set to oscillate, the wire is stretched and compressed by the two prongs. The stretching/compression force changes upon adsorption of analyte molecules onto/into the polymer wire, which is detected by the QTF with pico-Newton force sensitivity. An array of such sensors with different polymer wires is used for simultaneous detection of several analytes and for improvement of pattern recognition. The low cost (∼10¢) of the QTF, together with that an array of QTFs can be driven to oscillate simultaneously and their resonance frequencies detected with the same circuit, promises a high performance, low cost, and portable sensor for detecting various chemical vapors. We demonstrate here detection of parts-per-billion-level water, ethylnitrobenzene, and ethanol vapors using the QTF arrays

Detection of Heavy Metal Ions in Water by High-Resolution Surface Plasmon Resonance Spectroscopy Combined with Anodic Stripping Voltammetry

High-resolution differential surface plasmon resonance (SPR) with anodic stripping voltammetry (ASV) capability has been demonstrated for detecting heavy metal ions in water. Metal ions are electroplated onto the gold SPR sensing surface and are quantitatively detected by stripping voltammetry. Both the SPR angular shift and electrochemical current signal are recorded to identify the type and amount of the metal ions in water. The performance of the combined approach is further enhanced by a differential detection approach. The gold sensor surface is divided into a reference and a sensing area, and the difference in the SPR angles from the two areas is detected with a quadrant cell photodetector as a differential signal. Our system demonstrated quantitative detection of copper, lead, and mercury ions in water from part-per-million to sub-part-per-billion levels with good linearity

PM estimation via outdoor image analysis.

<p>PM estimation via outdoor image analysis.</p

Plasmonic-Based Imaging of Local Square Wave Voltammetry

Square wave voltammetry (SWV) is widely used in electrochemical analysis and sensors because of its high sensitivity and efficient rejection of background current, but SWV by the conventional electrochemical detection method does not provide spatial resolution. We report here a plasmonic method to image local SWV, which opens the door for analyzing heterogeneous electrochemical reactions and for high-throughput detections of microarrays. We describe the basic principle, validate the principle by comparing the plasmonic-based SWV with those obtained with the conventional method, and demonstrate imaging capability for local electrochemical analysis

Detection of Heavy Metal Ions in Drinking Water Using a High-Resolution Differential Surface Plasmon Resonance Sensor

We have built a high-resolution differential surface plasmon resonance (SPR) sensor for heavy metal ion detection. The sensor surface is divided into a reference and sensing areas, and the difference in the SPR angles from the two areas is detected with a quadrant cell photodetector as a differential signal. In the presence of metal ions, the differential signal changes due to specific binding of the metal ions onto the sensing area coated with properly selected peptides, which provides an accurate real-time measurement and quantification of the metal ions. Selective detection of Cu2+ and Ni2+ in the ppt−ppb range was achieved by coating the sensing surface with peptides NH2-Gly-Gly-His-COOH and NH2-(His)6-COOH. Cu2+ in drinking water was tested using this sensor