N, Fe co-incorporated CoO nanoarray enhanced by magnetic field for efficient water oxidation†
Abstract
CoO, as a typical water oxidation electrocatalyst, has gradually entered the bottleneck stage of performance modulation through composition optimization. Herein, the N, Fe co-bonded CoO was achieved by N plasma, which suggests further potential to be enhanced by a magnetic field during oxygen evolution reaction (OER) electrocatalysis. N atoms are a bridge for bonding Fe and Co centers, which serve as a fast channel for electron transfer. N, Fe co-doping decreases the electron density around Co2+ centers, which increases the unpaired electrons for electron acceptors. As a result, the intrinsic OER activities are boosted, which is further beneficial for amplifying the magnetic enhancement effect. The best performance emerges under a parallel magnetic field with 420 mT intensity, which results in a lowered overpotential of 217 mV and a Tafel slope of 25.1 mV dec−1 in alkaline media. The magnetic enhancement comes from the magnetohydrodynamic effect and the escape energy barrier reduction of the paramagnetic triplet state of O2. The magnetic enhancement effect would be amplified when the catalytic current becomes larger (magnetic current is 8 mA and 22 mA under 500 mA and 1000 mA total current, respectively). This work provides an in-depth insight into the magnetic enhancing mechanism and a highly feasible strategy for coupling heteroatoms with the magnetic field to operate and break through the bottleneck of non-noble electrocatalysis performance.