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  Enhanced oxygen evolution reaction activity of flower-like FeOOH via the synergistic effect of sulfur

Guo, R., He, Y., Yu, T., Cheng, P., You, J., Lin, H., et al. (2020). Enhanced oxygen evolution reaction activity of flower-like FeOOH via the synergistic effect of sulfur. Chemical Engineering Journal. doi:10.1016/j.cej.2020.127587.

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Guo, Rui1, Autor
He, Yan1, Autor
Yu, Tao1, Autor
Cheng, Peng1, Autor
You, Junhua1, Autor
Lin, Hongji1, Autor
Chen, Chien-Te1, Autor
Chan, Tingshan1, Autor
Liu, Xuanwen1, Autor
Hu, Zhiwei2, Autor           
Affiliations:
1External Organizations, ou_persistent22              
2Zhiwei Hu, Physics of Correlated Matter, Max Planck Institute for Chemical Physics of Solids, Max Planck Society, ou_1863461              

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 Zusammenfassung: Surface modification of electrocatalysts is a convenient strategy for addressing the drawbacks arising from the sluggish kinetics of the oxygen evolution reaction (OER). However, the preparation of electrocatalysts usually involves complex procedures, rendering investigation of the catalytic mechanism difficult. In this study, S-modified FeOOH electrocatalysts were prepared via a facile hydrothermal method at 120 °C. The electrocatalyst exhibited an outstanding OER performance with an overpotential of 254 mV at 50 mA·cm−2. Morphological, structural, and electrochemical characterizations revealed that Fe ion is the most important active center. The effect of S on the catalytic process was investigated based on the steric hindrance for OH* adsorption, changes in ΔG of the rate-determining step, and coordination mode of the active species. This is the first report on the formation of an (Fe-S)-O* bond that plays a key role in enhancing the electrochemical performance. © 2020 Elsevier B.V.

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Sprache(n): eng - English
 Datum: 2020-11-032020-11-03
 Publikationsstatus: Erschienen
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 Identifikatoren: DOI: 10.1016/j.cej.2020.127587
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Titel: Chemical Engineering Journal
Genre der Quelle: Zeitschrift
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Ort, Verlag, Ausgabe: Lausanne : Elsevier
Seiten: - Band / Heft: - Artikelnummer: - Start- / Endseite: - Identifikator: ISSN: 1385-8947
CoNE: https://pure.mpg.de/cone/journals/resource/954925622211