Promoting the formation of high-oxidation-state transition metal species in a hydroxide catalyst may improve its catalytic activity in the oxygen evolution reaction, which remains difficult to achieve with current synthetic strategies. Herein, we present a synthesis of single-layer NiFeB hydroxide nanosheets and demonstrate the efficacy of electron-deficient boron in promoting the formation of high-oxidation-state Ni for improved oxygen evolution activity. Raman spectroscopy, X-ray absorption spectroscopy, and electrochemical analyses show that incorporation of B into a NiFe hydroxide causes a cathodic shift of the Ni²⁺(OH)₂ → Ni^3+δOOH transition potential. Density functional theory calculations suggest an elevated oxidation state for Ni and decreased energy barriers for the reaction with the NiFeB hydroxide catalyst. Consequently, a current density of 100 mA cm^–2 was achieved in 1 M KOH at an overpotential of 252 mV, placing it among the best Ni-based catalysts for this reaction. This work opens new opportunities in electronic engineering of metal hydroxides (or oxides) for efficient oxygen evolution in water-splitting applications.

We report that fully alloyed Ag/Au nanospheres with high compositional homogeneity ensured by annealing at elevated temperatures show large extinction cross sections, extremely narrow bandwidths, and remarkable stability in harsh chemical environments. Nanostructures of Ag are known to have much stronger surface plasmon resonance than Au, but their applications in many areas have been very limited by their poor chemical stability against nonideal chemical environments. Here we address this issue by producing fully alloyed Ag/Au nanospheres through a surface-protected annealing process. A critical temperature has been found to be around 930 °C, below which the resulting alloy nanospheres, although significantly more stable than pure silver nanoparticles, can still gradually decay upon extended exposure to a harsh etchant. Nanospheres annealed above the critical temperature show a homogeneous distribution of Ag and Au, minimal crystallographic defects, and the absence of structural and compositional interfaces, which account for the extremely narrow bandwidths of the surface plasmon resonance and may enable many plasmonic applications with high performance and long lifetime, especially for those involving corrosive species.