By adding a small amount of a vesicle surfactant, “unavoidable” splashing is considerably reduced on superhydrophobic surfaces.

Surfaces designed to reduce the contact time of impacting droplets are potentially of great importance for fundamental science and technological applications, for example, anti-icing, self-cleaning and heating transfer applications. Previous studies have shown that the contact time can be reduced via introducing one or several crossing macroscale wires on superhydrophobic surfaces (SHSs). However, the impacts that strike far from the wires (off-center impacts) have contact times that are equal to those obtained on SHSs. Here we demonstrate that this problem can be largely solved by using macro anisotropic SHSs (macro-aniso-SHSs)—in which the wires are parallel and macroscaled. The droplet contact time depends on the spacing between the macrostripes and is remarkably reduced by 40–50% when the spacing is comparable to the droplet size. Obvious differences in the contact time are not observed for impacts that are centered on the stripe and in the groove. The impacts centered in the groove produce new hydrodynamics that are characterized by extended spreading, easy break up and bouncing in a flying-eagle configuration. The study discusses the underlying mechanisms of the impact processes. Moreover, the effect of parallel wires on the contact time is discussed by comparing the droplet impact data for grooved rice leaves and non-grooved cabbage leaves. The enhanced drop mobility associated with the macro-aniso-SHSs should be very useful in many industrial applications.

Compared with currently prevailing Li-ion technologies, sodium-ion energy storage devices play a supremely important role in grid-scale storage due to the advantages of rich abundance and low cost of sodium resources. As one of the crucial components of the sodium-ion battery and sodium-ion capacitor, electrode materials based on biomass-derived carbons have attracted enormous attention in the past few years owing to their excellent performance, inherent structural advantages, cost-effectiveness, renewability, etc. Here, a systematic summary of recent progress on various biomass-derived carbons used for sodium-ion energy storage (e.g., sodium-ion storage principle, the classification of bio-microstructure) is presented. Current research on the design principles of the structure and composition of biomass-derived carbons for improving sodium-ion storage will be highlighted. The prospects and challenges related to this will also be discussed. This review attempts to present a comprehensive account of the recent progress and design principle of biomass-derived carbons as sodium-ion storage materials and provide guidance in future rational tailoring of biomass-derived carbons.

Various photoactive building blocks can be incorporated into porous organic polymers (POPs). The intrinsic properties, such as various synthetic methods, outstanding inherent porosity, easy tunability, rigid conjugated skeletons and high stability, endow the polymeric organic networks with wonderful potential to act as heterogeneous photocatalytic platforms. However, exploitation of efficient synthetic strategies for metal-free and nontoxic heterogenous photocatalysts, and further insights into the photocatalytic process in organic transformations are still necessary. In this context, we report the concise synthesis of two polymeric frameworks (BTP-CMP and TBTP-CMP) incorporated into bithiophene and thiophthene units via a “bottom-up” strategy. BTP-CMP and TBTP-CMP were employed as heterogeneous photocatalysts in the synthesis of benzimidazoles, and exhibited excellent catalytic activity (up to 98% yield, at least 15 iterative runs). Therefore, the thiophene-embedded networks can serve as stable efficient and recyclable heterogeneous photocatalysts. Additionally, based on the catalytic results of control experiments and the energy band structures of the materials and intermediates, a possible photocatalytic reaction mechanism has been proposed.

This study discovered a “seesaw effect” in the underlying physics of the directional bouncing behavior of a droplet on superhydrophobic heterogeneous surfaces, leading to projectile motion.

Control of the directional bounce of droplets impacting solid surfaces is crucial for many agricultural and industrial applications. However, for the universal impact process of raindrops on plant leaves, little is known about how the highly coupled and complicated fluid–structure interaction controls the postimpact motion of droplets and endows the leaves with tenacious vitality. Here, we report a leaf‐like superhydrophobic cantilever to flexibly bounce droplets with well‐defined directionality and controllability. Through theoretical modeling and three‐dimensional fluid–solid coupling simulations, we find that the flexible cantilever significantly relieves the impacting forces of raindrops to reduce droplet fragmentation and enhance water repellency. The results further uncover the scaling relations of the droplet bouncing direction with respect to Weber number and cantilever stiffness. By this technique, the seemed disorganized postimpact movements of droplets are programmable and predictable, achieving the goal of where to point and where to hit automatically. This work advances the understanding of natural droplet impact phenomena, opens a new avenue for delicately controlling liquid motion in space with soft materials, and inspires a plethora of applications like soft robots to transport materials and energies, monitor plant growth as well as predict pathogen transmission in plants.