Detection of volatile organic compounds by weight-detectable sensors coated with metal-organic frameworks.

Detection of volatile organic compounds (VOCs) using weight-detectable quartz microbalance and silicon-based microcantilever sensors coated with crystalline metal-organic framework (MOF) thin films is described in this paper. The thin films of two MOFs were grown from COOH-terminated self-assembled monolayers onto the gold electrodes of sensor platforms. The MOF layers worked as the effective concentrators of VOC gases, and the adsorption/desorption processes of the VOCs could be monitored by the frequency changes of weight-detectable sensors. Moreover, the MOF layers provided VOC sensing selectivity to the weight-detectable sensors through the size-selective adsorption of the VOCs within the regulated nanospace of the MOFs.

Macroporous conductive polymer films fabricated by electrospun nanofiber templates and their electromechanical properties.

We demonstrate a facile method to fabricate macroporous poly (3,4-ethylenedioxythiophene)/poly (4-styrene sulfonate) (PEDOT/PSS) films with empty channels by using electrospun nanofiber as a sacrificial template. The channels within the PEDOT/PSS films were prepared by depositing PEDOT/PSS aqueous dispersion onto poly (vinyl pyrrolidone)/poly(methyl methacrylate) (PVP/PMMA) nanofiber template, and then the nanofibers were removed by solvent extraction. The average diameter of the channels is 313±45 nm, which is almost the same as the parent PVP/PMMA nanofibers. The macroporous PEDOT/PSS film with the empty channels showed an enhancement of electromechanical properties compared to the nonporous PEDOT/PSS film.

Rodlike macromolecules through spatial overlapping of thiophene dendrons.

Two novel dendritic macromonomers 7 and 8 functionalized with electroactive conjugated thiophene oligomers were synthesized by stepwise cross-coupling reactions and the introduction of a vinyl group at the focal point. Both macromonomers were polymerized into dendronized polymers 9 and 10 by using a radical polymerization method. The photophysical and redox behaviors of dendronized polymers 9 and 10 are significantly different from those of the corresponding macromonomers. This difference may result from the spatial overlapping of thiophene dendrons through π-π interactions when the dendrons are connected to a polymer backbone. The dendronized polymers can organize into large-area two-dimensional sheets with a thickness of 4.8 nm. Polymer 9, which has all-dendritic thiophene side chains, exhibited enhanced conductivity by partial doping with iodine or nitrosonium tetrafluoroborate (NOBF(4)). The novel amphiphilic dendronized polymer 15 was synthesized by the atom-transfer radical polymerization of macromonomer 7 from a poly(ethylene glycol) (PEG) macroinitiator and was found to have a self-organized structure in water.

Site-selective electroless nickel plating on patterned thin films of macromolecular metal complexes.

We demonstrate a simple route to depositing nickel layer patterns using photocross-linked polymer thin films containing palladium catalysts, which can be used as adhesive interlayers for fabrication of nickel patterns on glass and plastic substrates. Electroless nickel patterns can be obtained in three steps: (i) the pattern formation of partially quaterized poly(vinyl pyridine) by UV irradiation, (ii) the formation of macromolecular metal complex with palladium, and (iii) the nickel metallization using electroless plating bath. Metallization is site-selective and allows for a high resolution. And the resulting nickel layered structure shows good adhesion with glass and plastic substrates. The direct patterning of metallic layers onto insulating substrates indicates a great potential for fabricating micro/nano devices.