Despite highly promising characteristics of three-dimensionally (3D) nanostructured catalysts for the oxygen evolution reaction (OER) in polymer electrolyte membrane water electrolyzers (PEMWEs), universal design rules for maximizing their performance have not been explored. Here we show that woodpile (WP)-structured Ir, consisting of 3D-printed, highly-ordered Ir nanowire building blocks, improve OER mass activity markedly. The WP structure secures the electrochemically active surface area (ECSA) through enhanced utilization efficiency of the extended surface area of 3D WP catalysts. Moreover, systematic control of the 3D geometry combined with theoretical calculations and various electrochemical analyses reveals that facile transport of evolved O₂ gas bubbles is an important contributor to the improved ECSA-specific activity. The 3D nanostructuring-based improvement of ECSA and ECSA-specific activity enables our well-controlled geometry to afford a 30-fold higher mass activity of the OER catalyst when used in a single-cell PEMWE than conventional nanoparticle-based catalysts.

The way two liquids interact depends on how miscible they are. A remarkable phenomenon involving two miscible liquids is now reported: placing a drop of isopropanol on a water surface results in a Marangoni flow, and a static lens in the middle. Mixing and spreading of different liquids are omnipresent in nature, life and technology, such as oil pollution on the sea1,2, estuaries3, food processing4, cosmetic and beverage industries5,6, lab-on-a-chip devices7, and polymer processing8. However, the mixing and spreading mechanisms for miscible liquids remain poorly characterized. Here, we show that a fully soluble liquid drop deposited on a liquid surface remains as a static lens without immediately spreading and mixing, and simultaneously a Marangoni-driven convective flow is generated, which are counterintuitive results when two liquids have different surface tensions. To understand the dynamics, we develop a theoretical model to predict the finite spreading time and length scales, the Marangoni-driven convection flow speed, and the finite timescale to establish the quasi-steady state for the Marangoni flow. The fundamental understanding of this solutal Marangoni flow may enable driving bulk flows and constructing an effective drug delivery and surface cleaning approach without causing surface contamination by immiscible chemical species.

We investigate experimentally and theoretically how a droplet of a binary mixture evaporates when placed on a solid substrate. Our focus is the limit at which the two liquid components have different vapour pressures. Using physicochemical effects, we directly visualize the selective evaporation of the more volatile component and so document the space and time dependence of the chemical distribution in the droplet. In particular, we observe that a mixture consisting of an organic solvent and deionized water dissolves suspended fluorescent polystyrene particles if the lower volatility organic solvent reaches a critical concentration. Consequently, we show that for a small contact angle ( $\unicode[STIX]{x1D703}<\unicode[STIX]{x03C0}/2$ ) the suspended polystyrene particles begin to disappear from near the contact line, which indicates that the volatile component, here water, evaporates rapidly compared to the other component(s). Finally, we show that a diffusion-dominated model for evaporation of a binary mixture can predict well the experimental results where convective and diffusive mixing effects are negligible, in which case there is significant chemical segregation in the drop.

An acoustofluidic device for in-droplet microparticle washing and enrichment.