Electrochemically assisted synthesis of ultra-small Ru@IrOx core-shell nanoparticles for water splitting electro-catalysis
Carbon-free use of hydrogen as a clean fuel and a viable energy storage medium has been impeded by the efficiency of water electrolysis, which in turn, is limited by the bottleneck anodic oxygen evolution reaction (OER). The discovery of potentially efficient catalysts for OER is a key factor to fac...
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Veröffentlicht in: | Electrochimica acta 2020-05, Vol.341, p.136058, Article 136058 |
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Sprache: | eng |
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Zusammenfassung: | Carbon-free use of hydrogen as a clean fuel and a viable energy storage medium has been impeded by the efficiency of water electrolysis, which in turn, is limited by the bottleneck anodic oxygen evolution reaction (OER). The discovery of potentially efficient catalysts for OER is a key factor to facilitate the overall kinetics of water splitting, in which, noble metals such as Ru and Ir are still the conventional benchmarks. However, besides the high cost, such catalysts are also suffered from rapid performance degradation under OER conditions, particularly for Ru. In this work, Ru@IrOx core-shell nanoparticles (NPs) are successfully obtained through a wet chemical synthesis with the assistance of electro-oxidation. The NPs possess an ultra-small size of about 3.4 nm, achieving high specific OER activities of 51.99 μA/cm2oxide and 3.44 μA/cm2oxide as well as mass activities of 44.85 A/goxide and 3.03 A/goxide at overpotential of 250 mV (vs. RHE) in 0.1 M HClO4 and in 0.1 M KOH respectively. Furthermore, as-synthesized Ru@IrOx core-shell NPs are also proven to have excellent catalytic stability in both electrolytes, exhibiting great potential for application in both acidic and alkaline water electrolyzers.
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•Ru@IrOx core-shell NPs are prepared by an electrochemically assisted synthetic method.•Ru@IrOx NPs indicate an ultra-small particle size of about 3.4 nm.•As-synthesized Ru@IrOx NPs exhibit excellent OER activity and stability in both acidic and alkaline media. |
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ISSN: | 0013-4686 1873-3859 |
DOI: | 10.1016/j.electacta.2020.136058 |