A large-scale synthesis of heteroatom (N and S) co-doped hierarchically porous carbon (HPC) derived from polyquaternium for superior oxygen reduction reactivity
A simple, large-scale and green synthetic route is demonstrated for the preparation of polyquaternium derived heteroatom (N and S) co-doped hierarchically porous carbon (HPC). Our protocol allows for the simultaneous optimization of both porous structures and surface functionalities of (N and S) co-...
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Published in | Green chemistry : an international journal and green chemistry resource : GC Vol. 18; no. 9; pp. 2699 - 279 |
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Main Authors | , , , , , |
Format | Journal Article |
Language | English |
Published |
Royal Society of Chemistry
01.01.2016
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Subjects | |
Online Access | Get full text |
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Summary: | A simple, large-scale and green synthetic route is demonstrated for the preparation of polyquaternium derived heteroatom (N and S) co-doped hierarchically porous carbon (HPC). Our protocol allows for the simultaneous optimization of both porous structures and surface functionalities of (N and S) co-doped carbon (N-S-HPC). As a result, the obtained N-S-HPC shows a superior catalytic ORR performance to the commercial Pt/C catalyst in alkaline media, including high catalytic activity, remarkable long-term stability and strong methanol tolerance. Even in acidic media where most non-precious metal catalysts are suffered from high overpotential and low durability, our N-S-HPC exhibits an amazing ORR activity with a half-wave potential of 0.73V, and 40% enhanced limited diffusion-current density when compared to Pt/C catalyst. Particularly, when used for constructing a zinc–air battery cathode, such an N-S-HPC catalyst can give a discharge peak power density as high as 536 mW cm-2. At 1.0 V of cell voltage, a current density of 317 mA cm-2 is achieved. This performance is superior to all reported non-precious metal catalysts in literature for zinc–air batteries and significantly outperforms the state-of-the-art platinum-based catalyst. NRC publication: Yes |
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Bibliography: | 10.1039/c5gc02625c Electronic supplementary information (ESI) available. See DOI ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 1463-9262 1463-9270 1463-9270 |
DOI: | 10.1039/C5GC02625C |