| Autor: |
Xiang Yang, Baohui Zhu, Zhiyang Gao, Can Yang, Jingbo Zhou, Aijuan Han, Junfeng Liu |
| Jazyk: |
angličtina |
| Rok vydání: |
2024 |
| Předmět: |
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| Zdroj: |
Advanced Science, Vol 11, Iss 34, Pp n/a-n/a (2024) |
| Druh dokumentu: |
article |
| ISSN: |
2198-3844 |
| DOI: |
10.1002/advs.202306594 |
| Popis: |
Abstract Iron single‐atom catalysts (SACs) have garnered increasing attention as highly efficient catalysts for the oxygen reduction reaction (ORR), yet their performance in practical devices remains suboptimal due to the low density of accessible active sites. Anchoring iron single atoms on 2D support is a promising way to increase the accessible active sites but remains difficult attributing to the high aggregation tendency of iron atoms on the 2D support. Herein, a vacuum vapor deposition strategy is presented to fabricate an iron SAC supported on ultrathin N‐doped carbon nanosheets with densely active sites (FeSAs‐UNCNS). Experimental analyses confirm that the FeSAs‐UNCNS achieves densely accessible active sites (1.11 × 1020 sites g−1) in the configuration of Fe─N4O. Consequently, the half‐wave potential of FeSAs‐UNCNS in 0.1 m KOH reaches a remarkable value of 0.951 V versus RHE. Moreover, when employed as the cathode of various kinds of Zn–air batteries, FeSAs‐UNCNS exhibits boosting performances by achieving a maximum power density of 306 mW cm−2 and long cycle life (>180 h) at room temperature, surpassing both Pt/C and reported SACs. Further investigations reveal that FeSAs‐UNCNS facilitates the mass and charge transfer during catalysis and the atomic configuration favors the desorption of *OH kinetically. |
| Databáze: |
Directory of Open Access Journals |
| Externí odkaz: |
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