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Fe single-atom catalysts (Fe-SACs) have been extensively studied as a highly efficient electrocatalyst toward the oxygen reduction reaction (ORR). Nonetheless, they suffer from stability issue induced by dissolution of Fe metal center and the OH− blocking. Herein, a surface molecular engineering strategy is developed by using β-cyclodextrins (CDs) as a localized molecular encapsulation. The CD-modified Fe-SAC (Fe-SNC-β-CD) shows obviously improved activity toward the ORR with 0.90 V, 4.10 and 4.09 mA cm−2 for E1/2, J0 and Jk0.9, respectively. Meanwhile, the Fe-SNC-β-CD shows the excellent long-term stability against aggressive stress and the poisoning. It is confirmed through electrochemical investigation that modification of β-CD can, on one hand, regulate the atomic Fe coordination chemistry through the interaction between the CD and FeNx moiety, while on the other mitigate the strong adsorption of OH− and function as protective barrier against the poisoning molecules leading to enhanced ORR activity and stability for the Fe-SACs. The molecular encapsulation strategy demonstrates the uniqueness of post-pyrolysis surface molecular engineering for the design of single-atom catalyst.
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