Chromatic Conductive Polymer Nanocomposites of Poly (p-Phenylene Ethynylene)s and Single-Walled Carbon Nanotubes

We report on dispersions and thin films of chromatic conductive nanocomposites of poly(p-phenylene ethynylene)s (PPEs) and single-walled carbon nanotubes (SWNTs) generated via solution mixing. The linear, conjugated PPEs with dialkyl- and dialkyloxy-side chain groups are shown to debundle and disperse high concentration (up to 2.5 mg/mL) SWNTs in various organic solvents. The solubilization of SWNTs and PPE wrapping is accompanied with the change in the solution color. Ultraviolet visible absorption spectra of nanocomposite solutions demonstrate a new absorption peak at a higher wavelength, supporting the observed chromatism. Fluorescence spectra of nanocomposite solutions display significant quenching of the fluorescence intensity and the Stern–Volmer model is used to analyze fluorescence quenching. Electron microscopy of the chromatic solid films of high mass fraction PPE/SWNT nanocomposites obtained by vacuum filtration reveals the debundled SWNTs in the PPE matrix. The tensile strength and Young’s modulus of these PPE/SWNT nanocomposite films are as high as 150 MPa and 15 GPa, respectively. The composite films exhibit remarkably high conductivities, ranging from ~1000 S/m to ~10,000 S/m for 10 wt% and 60 wt% SWNT nanocomposites, respectively.

The Effect of Anchor Group on the Phonon Thermal Conductance of Single Molecule Junctions

There is a worldwide race to convert waste heat to useful energy using thermoelectric materials. Molecules are attractive candidates for thermoelectricity because they can be synthesised with the atomic precision, and intriguing properties due to quantum effects such as quantum interference can be induced at room temperature. Molecules are also expected to show a low thermal conductance that is needed to enhance the performance of thermoelectric materials. Recently, the technological challenge of measuring the thermal conductance of single molecules was overcome. Therefore, it is timely to develop strategies to reduce their thermal conductance for high performance thermoelectricity. In this paper and for the first time, we exploit systematically the effect of anchor groups on the phonon thermal conductance of oligo (phenylene ethynylene) (OPE3) molecules connected to gold electrodes via pyridyl, thiol, methyl sulphide and carbodithioate anchor groups. We show that thermal conductance is affected significantly by the choice of anchor group. The lowest and highest thermal conductances were obtained in the OPE3 with methyl sulphide and carbodithioate anchor groups, respectively. The thermal conductance of OPE3 with thiol anchor was higher than that with methyl sulphide but lower than the OPE3 with pyridyl anchor group.

Three-state molecular potentiometer based on a non-symmetrically positioned in-backbone linker

We report on the synthesis and single-molecule conductance of a para-oligo(phenylene)ethynylene (p-OPE) derivative with three well-defined conductance states. Employing theoretical models and comparing to reference compounds we show that this...

Self-assembly of chiral oligo(methylene-p-phenylene-ethynylene)s into vesicle-like particles independent of hydrophobicity/hydrophilicity of side chains and solvents

Chiral oligo(methylene-p-phenyleneethynylene)s can form vesicular assemblies no matter whether side chains and solvents are hydrophilic or hydrophobic. The self-assembly processes are highly independent of molecular design and chemical environments.

Calcium-induced reversible assembly of phosphorylated amphiphile within lipid bilayer membranes

Inspired by calcium-induced reversible assembly and disassembly of membrane proteins found in nature, here we developed a phosphorylated amphiphile (PA) that contains an oligo(phenylene-ethynylene) unit as a hydrophobic unit and...

Folding and duplex formation in mixed sequence recognition-encoded m-phenylene ethynylene polymers

One pot oligomerisation reactions give access to families of oligomers that allow facile analysis of folding propensity and assessment of suitability for sequence-selective duplex formation.