In Situ Self-Template Synthesis of Fe-N-Doped Double-Shelled Hollow Carbon Microspheres for Oxygen Reduction Reaction.
basic_science · Level V
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- Record sourced from PubMed, PMID 29286637.
- Also identified by DOI 10.1021/acsnano.7b05832.
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Abstract
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<sub>3</sub>O<sub>4</sub>) hollow microspheres as the templates, where pyrrole monomers were dispersed around the outer surface and prefilled the interior space. By adding hydrochloric acid, Fe<sup>3+</sup> ions were released to initiate polymerization of pyrrole on both the outer and inner surfaces of Fe<sub>3</sub>O<sub>4</sub> 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<sub>3</sub>O<sub>4</sub> hollow microspheres played trifunctional roles, i.e., the template to prepare a double-shelled hollow spherical structure, the initiator (i.e., Fe<sup>3+</sup> 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.