Answers are grounded in this paper and cite their sources.
Phase tailoring engineering of two-dimensional RuNi alloys was achieved via a host–guest exchange strategy, which endowed oxygen evolution reaction (OER) activity exceeding that of RuO2 to the RuNi (40:250) alloy with an fcc-Ni host and hcp-Ru guest as well as hydrogen evolution reaction (HER) activity exceeding that of Pt/C to the RuNi (250:40) alloy with an fcc/hcp-Ru host and fcc-Ni guest. X-ray photoelectron spectroscopy and in situ shell-isolated nanoparticle-enhanced Raman spectroscopy revealed that their differentiated surface reconstruction induced the respective two-site synergistic catalytic effect. The hcp-Ru site in the RuNi (40:250) alloy catalyzed the oxidation of OH– ions to O–O* and then generated a bridge-mode configuration of Ru–O–O–Ni by coupling with the adjacent Ni site to facilitate O2 evolution, while the fcc-Ru site in the RuNi (250:40) alloy acted as a transfer station for H2O by forming a Ru–OH2 adsorption state, followed by fabricating a bridge-mode configuration of Ru–HO–H–Ni through connection with the adjacent Ni site to promote H2O dissociation and H2 evolution. The integrated RuNi (40:250) || RuNi (250:40) electrolyzer achieved overall water splitting at 1.49 V (10 mA cm–2), outperforming the Pt/C || RuO2 benchmark (1.54 V), and stable operation for 650 h. This work provides fresh insights into phase-dependent dual-site synergistic catalytic behaviors for advanced alloy catalysts.
No takes yet. Share an insight, caveat, or question.
Hong et al. (2025) studied this question.
Synapse has enriched 10 related papers. Consider them for comparative context: