Abstract

AbstractA key challenge for the large‐scale application of the oxygen evolution reaction (OER) is the synthesis of active, cheap and robust catalysts. Here, a straightforward procedure to form novel porous and highly active multimetallic oxygen evolution catalysts was reported. They were derived from an original dendritic nickel foam (NiNF) using two strategies: i) Fe‐doping; and ii) Fe/Cr‐doping. A bimetallic NiFe catalyst, formed through controlled acid treatment followed by a simple galvanic exchange procedure proved remarkably active in 1 m KOH with a very low overpotential value of η200=276 mV at 200 mA cm−2 and a very low Tafel slope of 25 mV dec−1. A trimetallic FeNiCr catalyst, containing 11 % Cr, was also synthesised through electrodeposition and partial Cr leaching, to form a stable OER catalyst displaying a very low overpotential value of η200=279 mV at 200 mA cm−2 and a Tafel slope of 29 mV dec−1. These two novel catalysts are among the best performing OER catalysts reported so far.

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