“…[54,63,64] Another possible reason is the presence of Fe 3+ stimulating the oxidation of M 2+ (M:Coand Ni)toM 3+/4+ instead of its further oxidation to Fe 4+ . [56,57,65] As seen in Figure S23, the Ag 2 Oitself showed avery poor OER activity even in the presence of an excess amount of iron impurity.Therefore,itdoes make sense to postulate either (i) the interaction between Ag 2 Oa dsorbed by iron impurities and Co 3 O 4 or (ii)t he formation of new active species consisting of cobalt-silver-iron synergistically facilitated the OER kinetics.R esultantly,m uch higher current density at 1.7 V RHE was achieved on the activated Co 8 Ag oxide (211 mA cm À2 ), more than twice of that of Co 3 O 4 (102 mA cm À2 ). Even compared with the recent-reported benchmarked cobalt electrocatalysts,C o 8 Ag oxide displayed competitive catalytic performance,a slisted in Table S2.…”