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Abstract Superhydrophobic (SHPo) surfaces have been investigated vigorously since around 2000 due in large part to their unique potential for hydrodynamic frictional drag reduction without any energy or material input. The mechanisms and key factors affecting SHPo drag reduction have become relatively well understood for laminar flows by around 2010, as has been reviewed before [Lee et al. Exp Fluids 57:176 (2016)], but the progress for turbulent flows has been rather tortuous. While improved flow tests made positive SHPo drag reduction in fully turbulent flows more regular since around 2010, such a success in a natural, open water environment was reported only in 2020 [Xu et al. Phys Rev Appl 13:034056 (2020b)]. In this article, we review studies from the literature about turbulent flows over SHPo surfaces, with a focus on experimental studies. We summarize the key knowledge obtained, including the drag-reduction mechanism in the turbulent regime, the effect of the surface roughness morphology, and the fate and role of the plastron. This review is aimed to help guide the design and application of SHPo surfaces for drag reduction in the large-scale turbulent flows of field conditions. Graphic abstract 

For organic semiconductor crystals exhibiting anisotropic charge transport along different crystallographic directions, nanoconfinement is a powerful strategy to control crystal orientation by aligning the fast crystallographic growth direction(s) with the unconfined axis(es) of nanoconfining scaffolds. Here, design rules are presented to relate crystal morphology, scaffold geometry, and orientation control in solution-processed small-molecule crystals. Specifically, organic semiconductor triisopropylsilylethynyl pyranthrene needle-like crystals with a dimensionality of n = 1 and perylene platelike crystals with n = 2 were grown from solution within nanoconfining scaffolds comprising cylindrical nanopores with a dimensionality of m = 1, representing one unconfined dimension along the cylinder axis, and those comprising nanopillar arrays with a dimensionality of m = 2. For m = n systems, native crystal growth habits were preserved while the crystal orientation in n = m direction(s) was dictated by the geometry of the scaffold. For n ≠ m systems, on the other hand, orientation control was restricted within a single plane, either parallel or perpendicular to the substrate surface. Intriguingly, control over crystal shape was also observed for perylene crystals grown in cylindrical nanopores ( n > m ). Within the nanopores, crystal growth was restricted along a single direction to form a needle-like morphology. Once growth proceeded above the scaffold surface, the crystals adopted their native growth habit to form asymmetric T-shaped single crystals with concave corners. These findings suggest that nanoporous scaffolds with spatially-varying dimensionalities can be used to grow single crystals of complex shapes.