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Richard J Nichols

Publications and source records attributed to Richard J Nichols.

9 recordsLinked to original sources

Precision control of single-molecule electrical junctions.

There is much discussion of molecules as components for future electronic devices. However, the contacts, the local environment and the temperature can all affect their electrical properties. This sensitivity, particularly at the single-molecule level, may limit the use of molecules as active electrical components, and therefore it is important to design and evaluate molecular junctions with a robust and stable electrical response over a wide range of junction configurations and temperatures. Here we report an approach to monitor the electrical properties of single-molecule junctions, which involves precise control of the contact spacing and tilt angle of the molecule. Comparison with ab initio transport calculations shows that the tilt-angle dependence of the electrical conductance is a sensitive spectroscopic probe, providing information about the position of the Fermi energy. It is also shown that the electrical properties of flexible molecules are dependent on temperature, whereas those of molecules designed for their rigidity are not.

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Thermal gating of the single molecule conductance of alkanedithiols.

The temperature dependence of the single molecule conductance (SMC) of alpha,omega-alkanedithiols has been investigated using a scanning tunnelling microscopy (STM) method. This is based on trapping molecules between a gold STM tip and a gold substrate and measuring directly the current across the molecule under different applied potentials. A pronounced temperature dependence of the conductance, which scales logarithmically with T(1), is observed in the temperature range between 293 and 353 K. It is proposed the origin of this dependence is the change in distribution between molecular conformers rather than changes in either the conduction mechanism or the electronic structure of molecule. For alkanedithiols the time averaged conformer distribution shifts to less elongated conformers at higher temperatures thus giving rise to higher conductance across the molecular bridges. This is analysed by first calculating energy differences between different conformers and then calculating their partition distribution. A simple tunnelling model is then used to calculate the temperature dependent conductance based on the conformer distribution. These findings demonstrate that charge transport through single organic molecules at ambient temperatures is a subtle and highly dynamic process that cannot be described by analysing only one molecular conformation corresponding to the lowest energy geometry of the molecule.

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Molecular wire formation from viologen assemblies.

The adsorption behavior of viologen alpha,omega-dithiols (viologen dithiols) on gold has been investigated. At short exposures, a low-coverage phase consisting of flat-lying molecules has been determined by STM and IR spectroscopy. In contrast, multilayer films are formed after long adsorption times. Single molecular wires could be formed between a gold STM tip and a surface with a low coverage of the adsorbed dithiols, and their electrical behavior was investigated. Molecular conductivity was determined either by the repeated measurement of I(s) curves or by recording I-V curves for different tip-sample separations. These methods concurred in producing a value of (0.5 +/- 0.1) nS for the single-molecule conductivity of the alpha,omega-viologen dithiol molecule HS-6V6-SH. The high conductivity of HS-6V6-SH, as compared to that of HS-C12-SH, may be related to the low-lying LUMO, which provides a barrier indentation for electron transport in a two-step electron-transfer mechanism.

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Rational and combinatorial design of peptide capping ligands for gold nanoparticles.

Based on protein folding considerations, a pentapeptide ligand, CALNN, which converts citrate-stabilized gold nanoparticles into extremely stable, water-soluble gold nanoparticles with some chemical properties analogous to those of proteins, has been designed. These peptide-capped gold nanoparticles can be freeze-dried and stored as powders that can be subsequently redissolved to yield stable aqueous dispersions. Filtration, size-exclusion chromatography, ion-exchange chromatography, electrophoresis, and centrifugation can be applied to these particles. The effect of 58 different peptide sequences on the electrolyte-induced aggregation of the nanoparticles was studied. The stabilities conferred by these peptide ligands depended on their length, hydrophobicity, and charge and in some cases resulted in further improved stability compared with CALNN, yielding detailed design criteria for peptide capping ligands. A simple strategy for the introduction of recognition groups is proposed and demonstrated with biotin and Strep-tag II.

Amino Acid Sequence↗

Wiring nanoparticles with redox molecules.

Gold nanoparticles were used to make electrical contact to redox-active organic molecules. Viologen based dithiols were self-assembled from solution on Au(111) for use as tethers to attach nanoparticles to a conducting substrate. The topography and electrical properties of the resulting films were investigated by STM and STS and the orientation of these linkers was investigated by FTIR. Surface coverage increased with increasing reaction time, resulting in a change of film orientation from a flat to a more upright standing conformation. Gold nanoparticles attached to these self-assembled films were characterised by STM. It was possible to isolate a single redox-active molecule in an alkanethiol matrix and by subsequent attachment of a single gold nanoparticle the electrical properties of single wired molecules could be investigated. This method allowed the measurement of the conductivity of single molecules connecting a nanoparticle to the substrate chemically, thus forming stable electrical contacts at both ends.

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Redox state dependence of single molecule conductivity.

Spontaneous formation of stable molecular wires between a gold scanning tunneling microscopy (STM) tip and substrate is observed when the sample has a low coverage of alpha,omega-dithiol molecules and the tunneling resistance is made sufficiently small. Current-distance curves taken under these conditions exhibit characteristic current plateaux at large tip-substrate separations from which the conductivity of a single molecule can be obtained. The versatility of this technique is demonstrated using redox-active molecules under potential control, where substantial reversible conductivity changes from 0.5 to 2.8 nS were observed when the molecule was electrochemically switched from the oxidized to the reduced state.

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An FTIR study of the surface chemistry of the dynamic Si(100) surface during etching in alkaline solution.

In situ FTIR spectroscopy has been used in the attenuated total reflectance (ATR) mode to investigate the surface chemistry of etching Si(100) surfaces in aqueous KOH. The effect of solution concentration and electrode potential on the Si-H vibrations has been explored and the experimental results compared with density functional theory calculations. In addition. the kinetics of surface passivation of n-Si(100) has been investigated using FTIR spectroscopy.

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