Uri Sivan

DNA-templated assembly and electrode attachment of a conducting silver wire

Recent research in the field of nanometre-scale electronics has focused on two fundamental issues: the operating principles of small-scale devices, and schemes that lead to their realization and eventual integration into useful circuits. Experimental studies on molecular to submicrometre quantum dots and on the electrical transport in carbon nanotubes have confirmed theoretical predictions of an increasing role for charging effects as the device size diminishes. Nevertheless, the construction of nanometre-scale circuits from such devices remains problematic, largely owing to the difficulties of achieving inter-element wiring and electrical interfacing to macroscopic electrodes. The use of molecular recognition processes and the self-assembly of molecules into supramolecular structures, might help overcome these difficulties. In this context, DNA has the appropriate molecular-recognition and mechanical properties, but poor electrical characteristics prevent its direct use in electrical circuits. Here we describe a two-step procedure that may allow the application of DNA to the construction of functional circuits. In our scheme, hybridization of the DNA molecule with surface-bound oligonucleotides is first used to stretch it between two gold electrodes; the DNA molecule is then used as a template for the vectorial growth of a 12 µm long, 100 nm wide conductive silver wire. The experiment confirms that the recognition capabilities of DNA can be exploited for the targeted attachment of functional wires.

From repulsion to attraction and back to repulsion: the effect of NaCl, KCl, and CsCl on the force between silica surfaces in aqueous solution.

The force between silica surfaces in NaCl, KCl and CsCl aqueous solutions is studied at pH 5.5 using an atomic force microscope (AFM). As ion concentration is increased, more cations adsorb to the negatively charged silica, gradually neutralizing the surface charge, hence, suppressing the electrostatic double layer repulsion and revealing van der Waals attraction. At even higher salt concentrations, repulsion reemerges due to surface charge reversal by excess adsorbed cations. Adsorption grows monotonically with cation radius. At pH 5.5 the smallest ion, Na+, neutralizes the surface at 0.5-1 M, K+ at 0.2-0.5 M, and Cs+ at approximately 0.1 M. Titration with HCl to pH 4.0 shifts surface neutralization and charge reversal to lower salt concentrations compared with pH 5.5. When attraction dominates, the force curves are practically identical for the three salts, independent of their concentration.

The Governing Role of Surface Hydration in Ion Specific Adsorption to Silica: An AFM-Based Account of the Hofmeister Universality and Its Reversal

AFM measurements of the force acting between silica surfaces in the presence of varied alkali chloride salts and pHs elucidate the origin of the Hofmeister adsorption series and its reversal. At low pH, electrostatics is shown to be insignificant. The preferential adsorption of Cs(+) to the silica surface is traced to the weak hydration of neutral silanols and the resulting hydrophobic expulsion of weakly hydrated ions from bulk solution to the interface. The same interactions keep the strongly hydrated Na(+) and Li(+) in solution. As pH is increased, a tightly bound hydration layer forms on deprotonating silanols. Cs(+) is correspondingly expelled from the surface, and adsorption of small ions is encouraged. The deduced role of surface hydration is corroborated by hydration repulsion observed at high pH, surface overcharging at low pH, and data in other oxides.

Thermodynamic spin magnetization of strongly correlated two-dimensional electrons in a silicon inversion layer

A method invented to measure the minute thermodynamic magnetization of dilute two-dimensional fermions is applied to electrons in a silicon inversion layer. The interplay between the ferromagnetic interaction and disorderenhances the low temperature susceptibility up to 7.5 folds compared with the Pauli susceptibility of noninteracting electrons. The magnetization peaks in the vicinity of the density, where transition to strong localization takes place. At the same density, the susceptibility approaches the free spins value (Curie susceptibility), indicating an almost perfect compensation of the kinetic energy toll associated with spin polarization by the energy gained from the Coulomb correlation. Yet, the balance favors a paramagnetic phase over spontaneous magnetization in the whole density range.

Hollow nanoneedle array and its utilization for repeated administration of biomolecules to the same cells.

We present a novel hollow nanoneedle array (NNA) device capable of simultaneously delivering diverse cargo into a group of cells in a culture over prolonged periods. The silica needles are fed by a common reservoir whose content can be replenished and modified in real time while maintaining contact with the same cells. The NNA, albeit its submicrometer features, is fabricated in a silicon-on-insulator wafer using conventional, large scale, silicon technology. 3T3-NIH fibroblast cells and HEK293 human embryonic kidney cells are shown to grow and proliferate successfully on the NNAs. Cargo delivery from the reservoir through the needles to a group of HEK293 cells in the culture is demonstrated by repeated administration of fluorescently labeled dextran to the same cells and transfection with DNA coding for red fluorescent protein. The capabilities demonstrated by the NNA device open the door to large scale studies of the effect of selected cells on their environment as encountered, for instance, in the study of cell-fate decisions, the role of cell-autonomous versus nonautonomous mechanisms in developmental biology, and in the study of excitable cell-networks.

Self-assembly of nanoelectronic components and circuits using biological templates

Solid State Institute, Technion –Israel Institute of Technology,Haifa 32000, IsraelA multistep self-assembly process is proposed for the preparation of nanometer-scaleelectronics. The process is based onthe assembly of a DNA network that serves, in turn, as a template for the subsequent assembly of functional elements usingdifferent levels of molecular recognition ability. Inter-element connectivity and connection to the “macr oscopic world” isachieved by instilling electrical functionality to the DNA network. The feasibility of this approach was demonstrated by theDNA-templatedself-assembly of a 12 lm long, ca. 1000 A˚wide, conductive silver wire connecting two macroscopic elec-trodes.

Effect of Cation Size and Charge on the Interaction between Silica Surfaces in 1:1, 2:1, and 3:1 Aqueous Electrolytes

Application of two complementary AFM measurements, force vs separation and adhesion force, reveals the combined effects of cation size and charge (valency) on the interaction between silica surfaces in three 1:1, three 2:1, and three 3:1 metal chloride aqueous solutions of different concentrations. The interaction between the silica surfaces in 1:1 and 2:1 salt solutions is fully accounted for by ion-independent van der Waals (vdW) attraction and electric double-layer repulsion modified by cation specific adsorption to the silica surfaces. The deduced ranking of mono- and divalent cation adsorption capacity (adsorbability) to silica, Mg(2+) < Ca(2+) < Na(+) < Sr(2+) < K(+) < Cs(+), follows cation bare size as well as cation solvation energy but does not correlate with hydrated ionic radius or with volume or surface ionic charge density. In the presence of 3:1 salts, the coarse phenomenology of the force between the silica surfaces as a function of salt concentration resembles that in 1:1 and 2:1 electrolytes. Nevertheless, two fundamental differences should be noticed. First, the attraction between the silica surfaces is too large to be attributed solely to vdW force, hence implying an additional attraction mechanism or gross modification of the conventional vdW attraction. Second, neutralization of the silica surfaces occurs at trivalent cation concentrations that are 3 orders of magnitude smaller than those characterizing surface neutralization by mono- and divalent cations. Consequently, when trivalent cations are added to our cation adsorbability series the correlation with bare ion size breaks down abruptly. The strong adsorbability of trivalent cations to silica contrasts straightforward expectations based on ranking of the cationic solvation energies, thus suggesting a different adsorption mechanism which is inoperative or weak for mono- and divalent cations.

Short range attraction between two similarly charged silica surfaces

Using an atomic force microscope we measure the interaction between two identically charged silica surfaces in the presence of a saline solution. For pure NaCl the interaction is always repulsive. Upon addition of cobalt hexamine ions, Co(NH(3))(6)(+3), the repulsion is gradually suppressed and a pronounced attraction develops at distances much shorter than the screening length. Higher concentrations of cobalt hexamine turn the attraction back into repulsion. Measurements of surface charge renormalization by the trivalent cations provide their surface density and their association constant to the negatively charged silica surface. These estimates tend to exclude interaction between two condensed Wigner crystals as an explanation for the attraction.

Mixed alkanethiol monolayers on submicrometric gold patterns: a controlled platform for studying cell-ligand interactions.

Nanoscale organization of surface ligands often has a critical effect on cell-surface interactions. We have developed an experimental system that allows a high degree of control over the 2-D spatial distribution of ligands. As a proof of concept, we used the developed system to study how T-cell activation is independently affected by antigen density and antigen amount per cell. Arrays of submicrometer gold islands at varying surface coverage were defined on silicon by electron beam lithography (EBL). The gold islands were functionalized with alkanethiol self-assembled monolayers (SAMs) containing a small antigen, 2,4,6-trinotrophenyl (TNP), at various densities. Genetically engineered T-cell hybridomas expressing TNP-specific chimeric T-cell antigen receptor (CAR) were cultured on the SAMs, and their activation was assessed by IL-2 secretion and CD69 expression. It was found that, at constant antigen density, activation increased monotonically with the amount of antigen, while at constant antigen amount activation was maximal at an intermediate antigen density, whose value was independent of the amount of antigen.

The different effect of electron-electron interaction on the spectrum of atoms and quantum dots

Abstract:Though atoms and quantum dots typically contain a comparable number of electrons, the number of discrete levels resolved in spectroscopy experiments is very different for the two systems. In atoms, hundreds of levels are observed while in quantum dots that number is usually smaller than 10. In the present work, this difference is traced to the different confining potentials in these systems. In atoms, the soft confining potential leads to large spatial extent of the excited electrons wave function and hence to weak Coulomb interaction with the rest of the atomic electrons. The resulting level broadening is smaller than the single particle level spacing and decreases as the excitation energy is increased. In quantum dots, on the other hand, the sharp confining potential results in electron-electron scattering rates that grow rapidly with energy and fairly quickly exceed the approximately constant single particle level spacing. The number of discrete levels in quantum dots is hence limited by electron-electron interaction, whose effect is negligible in atoms.