Counterion-mediated micellar growth for cetyltrimethylammonium 2,6-dichlorobenzoate alone and together with cetyltrimethylammonium chloride has been investigated using small-angle scattering techniques. Variations in counterion composition at constant ionic strength cause large changes in micelle size. The selectivity coefficient for adsorption of the aromatic counterion over chloride ions at CTA+ surfaces has been determined. The effects of the two counterions on micellar surface potentials, together with 1H NMR chemical shift data, allow inferences to be drawn about the penetration of the aromatic counterion into the head group region of the micelles. The aromatic ion increases the surfactant-packing parameter by both increasing the average volume per surfactant monomer, a cosurfactant-like effect, and decreasing the area per head group by screening electrostatic repulsions. Counterions such as chloride, which show only surface adsorption, affect only area and are much less effective at driving micellar growth. Some comparisons are also made with literature data for CTABr.

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A new surface functionalization scheme for nano‐Bio field effect transistors (FETs) using biocompatible polyelectrolyte thin films (PET) is developed. PET assemblies on Si nanowires (Si‐NWs) are driven by electrostatic interactions between the positively charged polymer backbone and negatively charged Si/SiO2 surface. Such assemblies can be directly coated from PET aqueous solutions and result in a uniform nanoscale thin film, which is more stable compared to the conventional amine silanization. Short oligo‐ethylene glycol chains are grafted on the PETs to prevent nonspecific protein binding. Moreover, the reactive groups of the polymer chains can be further functionalized to other chemical groups in specific stoichiometry for biomolecules detection. Therefore, it opens a new strategy to precisely control the functional group densities on various biosensor surfaces at the molecular level. In addition, such assemblies of the polymers together with the bound analytes can be removed with the pH stimulation resulting in regeneration of a bare sensor surface without compromising the integrity and performance of the Si‐NWs. Thus, it is believed that the developed PET coating and sensing systems on Si‐NW FETs represent a versatile, promising approach for regenerative biosensors which can be applied to other biosensors and will benefit real device applications, enhancing sensor lifetime, reliability, and repeatability.

One-dimensional organic nanostructures are essential building blocks for high performance gas sensors. Constructing an e-nose type sensor array is the current golden standard in developing portable systems for the detection of gas mixtures. However, facile fabrication of nanoscale sensor arrays is still challenging due to the high cost of the conventional nanofabrication techniques. In this work, we fabricate a chemiresistive gas sensor array composed of well-ordered sub-100 nm wide conducting polymer nanowires using cost-effective nanoscale soft lithography. Poly(3,4-ethylene-dioxythiophene)-poly(styrene sulfonate) (PEDOT:PSS) nanowires functionalized with different self-assembled monolayers (SAMs) are capable of identifying volatile organic compounds (VOCs) at a low concentration range. The side chains and functional groups of the SAMs introduce different sensitivities and selectivities to the targeted analytes. The distinct response pattern of each chemical is subjected to pattern recognition protocols, which leads to a clear separation towards ten VOCs, including ketones, alcohols, alkanes, aromatics and amines. These results of the chemiresistive gas sensor array demonstrate that nanoscale soft lithography is a reliable approach for fabricating nanoscale devices and has the potential of mass producibility.

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