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Updated: May 29, 2025

The Synthesis, Characterization and Reactivity of a Series of Ruthenium N-triphosPh Complexes
Published on: April 10, 2015
Electron donation from carbon support enhances the activity and stability of ultrasmall ruthenium dioxide
Luo Huang1, Lixia Ma1, Jie Yang1
1Shaanxi Key Laboratory for Advanced Energy Devices, Shaanxi Engineering Lab for Advanced Energy Technology, School of Materials Science and Engineering, Shaanxi Normal University, Xi'an 710119 China.
Abstract:
Developing non-iridium (Ir)-based electrocatalysts with good stability and activity for acid oxygen evolution reaction (OER) is of great importance for electrocatalytic water splitting. Ruthenium dioxide (RuO2), which has lower price and higher OER activity, has been recognized as an attractive alternative to Ir-based electrocatalyst for acidic OER. However, the stability of most Ru-based electrocatalysts faces a great challenge in acidic condition. Here, a highly stable and active RuO2-based catalyst, tiny RuO2 nanoparticles inlaid onto carbon support (RuO2/C), is successfully prepared for acidic OER. Such a structure can efficiently inhibit the over-growth of RuO2 nanoparticles and prevent the agglomeration of RuO2 nanoparticles. Moreover, it is found that carbon support donate electron to RuO2 nanoparticles, which enhances the OER activity and stability of RuO2 during acidic OER. The RuO2/C exhibits an impressive OER performance with a low overpotential (197 mV at 10 mA cm-2) and low degradation rate (0.035 mV h-1) over a 450-h stability test in 0.5 M H2SO4, which are much better than the commercial Ir/C, RuO2 and the reported Ru-based electrocatalysts. This work provides an efficient strategy to simultaneously improve both stability and activity of Ru-based catalysts for acidic water oxidation.
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