Pressure-promoted highly-ordered Fe-doped-Ni2B for effective oxygen evolution reaction and overall water splitting

Accurate doping at special atomic sites can achieve effective control of active centers for the oxygen evolution reaction (OER), leading to the synthesis of active intermediates with higher conversion efficiency. Here we report the successful doping of Ni2B with Fe/Co to form highly ordered FeNiB and CoNiB electrocatalysts with a tetragonal Ni2B structure. A highly crystalline FeNiB electrode is found to have a very low polarization overpotential of 257 mV for the OER and a water splitting potential of 1.54 V at a current density of 10 mA cm(-2). XRD refinement, XPS and XAFS characterization found that doping with iron leads to the weakening of the bond strength of TM-B, which facilitates the adsorption of oxygen. During the OER process, the increasing dissolution of boron oxides promotes the effective exposure of metal active centers and boosts the catalytic performance. Theoretical calculations reveal that the substitution of Fe atoms in Ni2B make its DOS near the Fermi level higher by 2.78 times compared to that of the original Ni2B, which helps to increase the electronic conductivity and the catalytic performance.

Automated summary

Accurate doping at special atomic sites can effectively control the active centers for the oxygen evolution reaction (OER). Doping Fe/Co into Ni2B forms highly ordered FeNiB and CoNiB electrocatalysts, which exhibit low overpotential and high water splitting potential. The substitution of Fe atoms in Ni2B increases the electronic conductivity and catalytic performance, leading to enhanced OER efficiency.