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Boosting oxygen evolution of single-atomic ruthenium through electronic coupling with cobalt-iron layered double hydroxides

Single atom catalyst, which contains isolated metal atoms singly dispersed on supports, has great potential for achieving high activity and selectivity in hetero-catalysis and electrocatalysis. However, the activity and stability of single atoms and their interaction with support still remains a mys...

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Bibliographic Details
Published in:Nature communications 2019-04, Vol.10 (1), p.1711-1711, Article 1711
Main Authors: Li, Pengsong, Wang, Maoyu, Duan, Xinxuan, Zheng, Lirong, Cheng, Xiaopeng, Zhang, Yuefei, Kuang, Yun, Li, Yaping, Ma, Qing, Feng, Zhenxing, Liu, Wen, Sun, Xiaoming
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Language:English
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Summary:Single atom catalyst, which contains isolated metal atoms singly dispersed on supports, has great potential for achieving high activity and selectivity in hetero-catalysis and electrocatalysis. However, the activity and stability of single atoms and their interaction with support still remains a mystery. Here we show a stable single atomic ruthenium catalyst anchoring on the surface of cobalt iron layered double hydroxides, which possesses a strong electronic coupling between ruthenium and layered double hydroxides. With 0.45 wt.% ruthenium loading, the catalyst exhibits outstanding activity with overpotential 198 mV at the current density of 10 mA cm −2 and a small Tafel slope of 39 mV dec −1 for oxygen evolution reaction. By using operando X-ray absorption spectroscopy, it is disclosed that the isolated single atom ruthenium was kept under the oxidation states of 4+ even at high overpotential due to synergetic electron coupling, which endow exceptional electrocatalytic activity and stability simultaneously. While water splitting offers a carbon-neutral means to store energy, water oxidation is sluggish and corrosive over earth-abundant electrocatalysts. Here, authors show single ruthenium atoms over cobalt-iron layered double hydroxides to be effective and stable oxygen evolution electrocatalysts.
ISSN:2041-1723
2041-1723
DOI:10.1038/s41467-019-09666-0