A Two‐in‐One Strategy to Simultaneously Boost the Site Density and Turnover Frequency of Fe−N−C Oxygen Reduction Catalysts

Site density and turnover frequency are the two fundamental kinetic descriptors that determine the oxygen reduction activity of iron-nitrogen-carbon (Fe-N-C) catalysts. However, it remains a grand challenge to simultaneously optimize these two parameters in a single Fe-N-C catalyst. Here we show that treating a typical Fe-N-C catalyst with ammonium iodine (NH4I) vapor via a one-step chemical vapor deposition process not only increases the surface area and porosity of the catalyst (and thus enhanced exposure of active sites) via the etching effect of the in-situ released NH3, but also regulates the electronic structure of the Fe-N4 moieties by the iodine dopants incorporated into the carbon matrix. As a result, the NH4I-treated Fe-N-C catalyst possesses both high values in the site density of 2.15×1019 sites g-1 (×2 enhancement compared to the untreated counterpart) and turnover frequency of 3.71 electrons site-1 s-1 (×3 enhancement) that correspond to a high mass activity of 12.78 A g-1, as determined by in-situ nitrite stripping technique. Moreover, this catalyst exhibits an excellent oxygen reduction activity in base with a half-wave potential (E1/2) of 0.924 V and acceptable activity in acid with E1/2 = 0.795 V, and superior power density of 249.1 mW cm-2 in zinc-air batteries.