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W/W2C heterostructured nanoparticles encapsulated by N,P dual-doped carbon (W/W2C@NPC) fabricated by the carbonization of in situ polymerized polyaniline (PANI) and phosphotungstic acid require low overpotentials of 55 mV and 82 mV vs. RHE to achieve a cathodic current density of 10 mA cm−2 in acidic and alkaline electrolytes, respectively. [ABSTRACT FROM AUTHOR]

Here, we report a facile method to synthesize ruthenium phosphides with diameter 1 nm and an amorphous structure at room temperature. Only 31 mV vs. RHE overpotential is required to deliver 10 mA cm−2 and no degradation in hydrogen evolution reaction (HER) performance is recorded after 24 h of catalysis at 100 mA cm−2. [ABSTRACT FROM AUTHOR]

Precise control over the configuration, size and density of Au nanoparticles (NPs) has offered an efficient route to enhance and optimize the performance and usability of various NP-based applications. In this study we successfully demonstrate precise control of the configuration, size and density of self-assembled Au nanostructures on 4H-SiC (0001) via systematic variation of the deposition amount, annealing temperature and duration. Depending on the deposition amount at a fixed annealing temperature and duration, the self-assembled Au NPs are successfully fabricated based on the Volmer–Weber growth model, and the NPs nucleate as round dome shapes and evolve into hexagonal nano-crystals with facet formation along with the increased deposition amounts. For the variation of annealing temperature, the Au nanostructures radically develop into two distinct regimes: i.e. irregular Au nano-mounds (regime I) between 400 and 700 °C based on the diffusion limited agglomeration (DLA) model and round dome-shaped droplets (DPs) (regime II) between 750 and 1000 °C. The dwelling time, size and density evolution of the round dome-shaped Au DPs are discussed based on the Ostwald ripening theory. [ABSTRACT FROM AUTHOR]