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Herein, we reported a special Fe–N-doped double-shelled hollow carbon microsphere (Fe–N-DSC) which was prepared by a facile, in situ polymerization followed by pyrolysis. With porous ferroferric oxide (Fe 3 O 4 ) hollow microspheres as the templates, where pyrrole monomers were dispersed around the outer surface and prefilled the interior space. By adding hydrochloric acid, Fe 3+ ions were released to initiate polymerization of pyrrole on both the outer and inner surfaces of Fe 3 O 4 microspheres until they were completely dissolved, resulting in the Fe-containing polypyrrole double-shelled hollow carbon microspheres (Fe-PPY-DSC). The Fe-PPY-DSC was then pyrolyzed to generate the Fe-N-DSC. The Fe 3 O 4 hollow microspheres played trifunctional roles, i.e., the template to prepare a double-shelled hollow spherical structure, the initiator ( i.e., Fe 3+ ions) for the polymerization of pyrrole, and the Fe source for doping. The Fe–N-DSC exhibited a superior catalytic activity for oxygen reduction as comparable to commercial Pt/C catalysts in both alkaline and acidic media. The high catalytic performance was ascribed to the special porous double-shelled hollow spherical structure, which provided more active sites and was beneficial to a high-flux mass transportation.
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Huang et al. (2017) studied this question.
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