Tuning the Fe-N4 sites by introducing Bi-O bond in Fe-N-C system for promoting oxygen reduction reaction

Elemental Bi is effective in optimizing the electrocatalytic activity of perovskite oxides and noble metals, but has never been used to adjust the oxygen reduction activity of Fe/N-C catalysts. Here, in order to introduce the Bi element into the Fe/N-C system with atomic-level dispersion, by means of a rod-like C3N4 template carrying with Fe and Bi atoms as a sacrificial agent, we successfully dope Bi atoms into the ZIF-8 derived Fe/N-C carbon system with a porous rod-like structure in the form of Bi-O (Fe/Bi-RNC). Mossbauer spectroscopy and electron paramagnetic resonance tests prove that Bi doping leads to the formation of higher active Fe-N sites in Fe/Bi-RNC. The oxygen reduction reaction (ORR) of as-prepared Fe/Bi-RNC is highly superior to the catalyst without Bi doping (Fe-RNC) in both alkaline and acidic electrolytes. Density functional theory (DFT) calculation results further unveil that the existence of the Bi-O bond reduces the band gap of Fe-N4, and their cooperation is very favorable for electron transfer in the ORR rate-determining step, thereby triggering excellent oxygen reduction performance. These findings demonstrate that Bi atoms have a facilitating role in Fe/N-C oxygen reduction catalysts.