For several centuries fluid dynamics studies have relied upon the assumption that when a liquid flows over a solid surface, the liquid molecules adjacent to the solid are stationary relative to the solid. This no-slip boundary condition (BC) has been applied successfully to model many macroscopic experiments, but has no microscopic justification. In recent years there has been an increased interest in determining the appropriate BCs for the flow of Newtonian liquids in confined geometries, partly due to exciting developments in the fields of microfluidic and microelectromechanical devices and partly because new and more sophisticated measurement techniques are now available. An increasing number of research groups now dedicate great attention to the study of the flow of liquids at solid interfaces, and as a result a large number of experimental, computational and theoretical studies have appeared in the literature. We provide here a review of experimental studies regarding the phenomenon of slip of Newtonian liquids at solid interfaces. We dedicate particular attention to the effects that factors such as surface roughness, wettability and the presence of gaseous layers might have on the measured interfacial slip. We also discuss how future studies might improve our understanding of hydrodynamic BCs and enable us to actively control liquid slip.

Polymers are lightweight, flexible, solution-processable materials that are promising for low-cost printed electronics as well as for mass-produced and large-area applications. Previous studies demonstrated that they can possess insulating, semiconducting or metallic properties; here we report that polymers can also be semi-metallic. Semi-metals, exemplified by bismuth, graphite and telluride alloys, have no energy bandgap and a very low density of states at the Fermi level. Furthermore, they typically have a higher Seebeck coefficient and lower thermal conductivities compared with metals, thus being suitable for thermoelectric applications. We measure the thermoelectric properties of various poly(3,4-ethylenedioxythiophene) samples, and observe a marked increase in the Seebeck coefficient when the electrical conductivity is enhanced through molecular organization. This initiates the transition from a Fermi glass to a semi-metal. The high Seebeck value, the metallic conductivity at room temperature and the absence of unpaired electron spins makes polymer semi-metals attractive for thermoelectrics and spintronics.

The reduced pressure synthesis of poly(3,4-ethylenedioxythiophene) (PEDOT) with sheet-like morphology has been achieved with the introduction of an amphiphilic triblock copolymer into the oxidant thin film. Addition of the copolymer not only results in an oxidant thin film which remains liquid-like under reduced pressure but also induces structured growth during film formation. PEDOT films were polymerized using the vacuum vapor phase polymerization (VPP) technique, in which we show that maintaining a liquid-like state for the oxidant is essential. The resulting conductivity is equivalent to commercially available indium tin oxide (ITO) with concomitant optical transmission values. PEDOT films can be produced with a variety of thicknesses across a range of substrate materials from plastics to metals to ceramics, with sheet resistances down to 45 Ω/□ (ca. 3400 S•cm −1 ), and transparency in the visible spectrum of >80% at 65 nm thickness. This compares favorably to ITO and its currently touted replacements.

Suspended microdevices are employed to measure the in-plane electrical conductivity, thermal conductivity, and Seebeck coefficient of suspended poly(3,4-ethylenedioxythiophene) (PEDOT) thin films. The measured thermal conductivity is higher than previously reported for PEDOT and generally increases with the electrical conductivity. The increase exceeds that predicted by the Wiedemann-Franz law for metals and can be explained by significant electronic thermal transport in PEDOT.

Funding Agencies|US National Science Foundation Thermal Transport Processes Program [CBET-0933454]; European Research Council (ERC) [307596]; Swedish foundation for strategic research; Knut and Alice Wallenberg foundation; Swedish Energy Agency; NSF Graduate Research Fellowship Program

Superhydrophobic coatings are reported as promising candidates for anti-icing applications. Various studies have shown that as well as having ultra water repellency the surfaces have reduced ice adhesion and can delay water freezing. However, the structure or texture (roughness) of the superhydrophobic surface is subject to degradation during the thermocycling or wetting process. This degradation can impair the superhydrophobicity and the icephobicity of those coatings. In this review, a brief overview of the process of droplet freezing on superhydrophobic coatings is presented with respect to their potential in anti-icing applications. To support this discussion, new data is presented about the condensation of water onto physically decorated substrates, and the associated freezing process which impacts on the freezing of macroscopic droplets on the surface.