| Abstract: | Among the bifunctional catalysts for water splitting, recently emerged transition‐metal single‐atom catalysts are theoretically considered to possess high potential, while the experimental activity is not satisfactory yet. Herein, an exceptionally efficient trifunctional metal–nitrogen–carbon (M–N–C) catalyst electrode, composed of a hierarchical carbon matrix embedding isolated nickel atoms with nickel–iron (NiFe) clusters, is presented. 1D microfibers and nanotubes grow sequentially from 2D nanosheets as sacrificial templates via two stages of solution‐ and solid‐phase reactions to form a 1D hierarchy. Exceptionally efficient bifunctional activity with an overpotential of only 13 mV at 10 mA cm?2 toward hydrogen evolution reaction (HER) and an overpotential of 210 mV at 30 mA cm?2 toward oxygen evolution reaction (OER) is obtained, surpassing each monofunctional activity ever reported. More importantly, an overpotential of only 126 and 326 mV is required to drive 500 mA cm?2 toward the HER and OER, respectively. For the first time, industrial‐scale water splitting with two bifunctional catalyst electrodes with a current density of 500 mA cm?2 at a potential of 1.71 V is demonstrated. Lastly, trifunctional catalytic activity including oxygen reduction reaction is also proven with a half‐wave potential at 0.848 V. |
