Abstract
Single atom Fe-nitrogen-carbon (Fe-N-C) catalysts have high catalytic activity and selectivity for the oxygen reduction reaction (ORR), and are possible alternatives for Pt-based materials. However, the reasonable design and selection of precursors to establish their relationship with Fe-N-C catalyst performance is still a formidable task. Herein, precursors with controllable structures are easily achieved through isomer engineering, with the purpose of regulating the active site density and microscopic morphology of the final electrocatalyst. As-proof-of-concept, phenylenediamine isomers-based polymers are used as precursors to fabricate Fe-N-C catalysts. The Fe-PpPD-800 derived from p-phenylenediamine shows that the best ORR activity with a half-wave potential (E1/2 ) reaches 0.892 V vs reversible hydrogen electrode (RHE), which is better than the counterparts derived from o-phenylenediamine (Fe-PoPD-800) and m-phenylenediamine (Fe-PmPD-800), even surpassing commercial Pt/C (E1/2 = 0.881 V vs RHE). Furthermore, the self-made zinc-air battery based on Fe-PpPD-800 achieves high power density and specific capacity up to 242 mW cm-2 and 873 mA h gZn -1 respectively, a stable open circuit voltage of 1.45 V, and excellent cycling stability. This work not only proves the practicability of adjusting the catalytic activity of single-atom catalysts through isomer engineering, but also provides an approach to understand the relationship between precursors and target catalysts performance.
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