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 inGreen chemistry : an international journal and green chemistry resource : GC Vol. 18; no. 9; pp. 2699 - 279
Main Authors Wu, Mingjie, Qiao, Jinli, Li, Kaixi, Zhou, Xuejun, Liu, Yuyu, Zhang, Jiujun
Format Journal Article
LanguageEnglish
Published Royal Society of Chemistry 01.01.2016
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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
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