Electronic modulation and proton transfer by iron and borate co-doping for synergistically triggering the oxygen evolution reaction on a hollow NiO bipyramidal prism

Designing an Earth-abundant and inexpensive electrocatalyst to drive the oxygen evolution reaction (OER) for high-purity hydrogen production is of great importance. Herein, the cation (iron) and anion (borate) co-doping strategy was proposed to effectively trigger the OER performance on a low-cost NiO material. The optimal hollow Fe/B-i-NiO bipyramidal prism shows superior OER performance, and displays a low overpotential (261 mV) at 10 mA cm(-2), accompanied by a low Tafel slope (46 mV dec(-1)), excellent intrinsic activity and robust stability. The overall alkaline water splitting using Fe/B-i-NiO/NF as an anode affords low cell voltages of 1.50 and 1.63 V at 10 and 100 mA cm(-2), and operates steadily at a high current density of 100 mA cm(-2) for 55 h without decay. The excellent electrocatalytic activity could be ascribed to the hollow structure to shorten the mass transfer pathway, the electronic modulation by Fe doping, the increased accessible electroactive sites created by oxygen vacancies through borate doping, and the formation of BO33--OH- to accelerate the deprotonation of OHads.

Automated summary

The cation and anion co-doping strategy proposed in this study effectively enhanced the OER performance on a low-cost NiO material, resulting in superior OER activity for high-purity hydrogen production. The excellent electrocatalytic activity of the Fe/B-i-NiO bipyramidal prism can be attributed to its hollow structure, electronic modulation by Fe doping, increased accessible electroactive sites through borate doping, and the formation of BO33--OH- to accelerate the deprotonation of OHads.