Novel (Pt-Ox )-(Co-Oy ) Nonbonding Active Structures on Defective Carbon from Oxygen-Rich Coal Tar Pitch for Efficient HER and ORR
© 2022 Wiley-VCH GmbH.
| Publié dans: | Advanced materials (Deerfield Beach, Fla.). - 1998. - 34(2022), 45 vom: 16. Nov., Seite e2206960 |
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| Auteur principal: | |
| Autres auteurs: | , , , , , |
| Format: | Article en ligne |
| Langue: | English |
| Publié: |
2022
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| Accès à la collection: | Advanced materials (Deerfield Beach, Fla.) |
| Sujets: | Journal Article (Pt-Ox)-(Co-Oy) sites CTP-derived defective carbon electrocatalysis nonbonding structures |
| Résumé: | © 2022 Wiley-VCH GmbH. Atomic-scale utilization and coordination structure of Pt electrocatalyst is extremely crucial to decrease loading mass and maximize activity for hydrogen evolution reactions (HERs) and oxygen reduction reactions (ORRs). A novel atomic-scale (Pt-Ox )-(Co-Oy ) nonbonding active structure is designed and constructed by anchoring Pt single atoms and Co atomic clusters on the defective carbon derived from oxygen-rich coal tar pitch (CTP). The Pt loading mass is extremely low and only 0.56 wt%. A new nonbonding interaction phenomenon between Pt-Ox and Co-Oy is found and confirmed based on X-ray absorption spectroscopy and density functional theory calculations. Based on the (Pt-Ox )-(Co-Oy ) nonbonding active structure, surface chemical field coupling with electrocatalysis for the HER and ORR is confirmed. It is found that the (Pt-Ox )-(Co-Oy ) nonbonding active structure exhibits high mass activities of 64.4 A cm-2 mgPt -1 (at an overpotential of 100 mV) and 7.2 A cm-2 mgPt -1 (at 0.8 V vs reversible hydrogen electrode) for the HER and ORR, respectively. The values are 6.5 and 11.6 times as much as those of commercial 20% Pt/C. The work provides innovative insight to design and understand efficient active sites of atomic-scale Pt on oxygen-rich CTP-derived carbon supports for electrocatalysis |
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| Description: | Date Revised 10.11.2022 published: Print-Electronic Citation Status PubMed-not-MEDLINE |
| ISSN: | 1521-4095 |
| DOI: | 10.1002/adma.202206960 |