Efficient water oxidation with amorphous transition metal boride catalysts synthesized by chemical reduction of metal nitrate salts at room temperature
|dc.identifier.citation||Yang, Y. and Zhuang, L. and Rufford, T. and Wang, S. and Zhu, Z. 2017. Efficient water oxidation with amorphous transition metal boride catalysts synthesized by chemical reduction of metal nitrate salts at room temperature. RSC Advances. 7 (52): pp. 32923-32930.|
© 2017 The Royal Society of Chemistry. We present a variety of amorphous transition-metal borides prepared at room temperature by a chemical reduction method as highly active catalysts for the oxygen evolution reaction (OER). The amorphous borides exhibit activities much higher than the corresponding crystalline (spinel, layered double hydroxide and perovskite) metal oxides containing the identical metal compositions, which have already been regarded as promising OER catalysts. The amorphous Ni/Fe borides showed the best mass normalized OER current density of 50 A g -1 at an overpotential of 0.35 V, transcending the performance of the state-of-the-art OER catalyst, RuO 2 . Amorphous transition-metal borides demonstrated extremely high active OER catalytic activity. The outstanding catalytic activity can be attributed to the amorphous structure, the large specific surface areas (above 110 m 2 g -1 ) and the electron-enriched transition metal sites stemming from boron doping. The stoichiometry of the catalysts can be controlled precisely even for the synthesis of quaternary metal boride catalysts, which made it feasible to further optimize the catalytic activity. These results indicated that it is facile to prepare highly active OER catalysts by the one-step chemical reduction process at room temperature.
|dc.publisher||Royal Society of Chemistry|
|dc.title||Efficient water oxidation with amorphous transition metal boride catalysts synthesized by chemical reduction of metal nitrate salts at room temperature|
|curtin.department||Department of Chemical Engineering|
|curtin.accessStatus||Fulltext not available|
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