Boosting cascade electron transfer in NiFe oxyhydroxide for overall water splitting.

Nickel–iron oxyhydroxides are among the most active electrocatalysts, but their sluggish kinetic of oxygen evolution reaction (OER) limits the energy efficiency toward overall water splitting. Here, we present a "cascade electron transfer" strategy through spurring unidirectional electron transfer among different metal sites in Mn-doped FeNiOOH@FeNiP to boost OER and overall water splitting. The Mn doping induces a cascade electron transfer from Ni to Fe and then to Mn via metal-O-metal bridge, thus promoting the oxidation Ni and Fe centers, which in turn help charge transfer by increasing the covalency between metal-O bonds to optimize the bonding strength between metal and adsorbed oxygen species. Consequently, the optimal Mn–FeNiOOH@FeNiP delivers a fast OER kinetics (32.1 mV dec−1) along with a low overpotential of 215 mV@10 mA cm−2. Benefiting from the synergistic effect of high conductivity, large specific surface area, and favorable OER kinetics, the catalyst only requires a low cell voltage of 1.456 V to achieve 20 mA cm−2 for overall water splitting, superior to that of a commercial RuO2ǁPt/C catalyst. [ABSTRACT FROM AUTHOR]