Vacancy Defects Inductive Effect of Asymmetrically Coordinated Single-Atom Fe─N3 S1 Active Sites for Robust Electrocatalytic Oxygen Reduction with High Turnover Frequency and Mass Activity

© 2023 Wiley-VCH GmbH.

Bibliographische Detailangaben
Veröffentlicht in:Advanced materials (Deerfield Beach, Fla.). - 1998. - 36(2024), 11 vom: 01. März, Seite e2308243
1. Verfasser: Zhao, Yilin (VerfasserIn)
Weitere Verfasser: Chen, Hsiao-Chien, Ma, Xuelu, Li, Jiaye, Yuan, Qing, Zhang, Peng, Wang, Minmin, Li, Junxi, Li, Min, Wang, Shifu, Guo, Han, Hu, Ruanbo, Tu, Kun-Hua, Zhu, Wei, Li, Xuning, Yang, Xuan, Pan, Yuan
Format: Online-Aufsatz
Sprache:English
Veröffentlicht: 2024
Zugriff auf das übergeordnete Werk:Advanced materials (Deerfield Beach, Fla.)
Schlagworte:Journal Article controllable synthesis electrocatalysis oxygen reduction reaction single-atom catalyst
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520 |a The development of facile, efficient synthesis method to construct low-cost and high-performance single-atom catalysts (SACs) for oxygen reduction reaction (ORR) is extremely important, yet still challenging. Herein, an atomically dispersed N, S co-doped carbon with abundant vacancy defects (NSC-vd) anchored Fe single atoms (SAs) is reported and a vacancy defects inductive effect is proposed for promoting electrocatalytic ORR. The optimized catalyst featured of stable Fe─N3 S1 active sites exhibits excellent ORR activity with high turnover frequency and mass activity. In situ Raman, attenuated total reflectance surface enhanced infrared absorption spectroscopy reveal the Fe─N3 S1 active sites exhibit different kinetic mechanisms in acidic and alkaline solutions. Operando X-ray absorption spectra reveal the ORR activity of Fe SAs/NSC-vd catalyst in different electrolyte is closely related to the coordination structure. Theoretical calculation reveals the upshifted d band center of Fe─N3 S1 active sites facilitates the adsorption of O2 and accelerates the kinetics process of *OH reduction. The abundant vacancy defects around the Fe─N3 S1 active sites balance the OOH* formation and *OH reduction, thus synergetically promoting the electrocatalytic ORR process 
650 4 |a Journal Article 
650 4 |a controllable synthesis 
650 4 |a electrocatalysis 
650 4 |a oxygen reduction reaction 
650 4 |a single-atom catalyst 
700 1 |a Chen, Hsiao-Chien  |e verfasserin  |4 aut 
700 1 |a Ma, Xuelu  |e verfasserin  |4 aut 
700 1 |a Li, Jiaye  |e verfasserin  |4 aut 
700 1 |a Yuan, Qing  |e verfasserin  |4 aut 
700 1 |a Zhang, Peng  |e verfasserin  |4 aut 
700 1 |a Wang, Minmin  |e verfasserin  |4 aut 
700 1 |a Li, Junxi  |e verfasserin  |4 aut 
700 1 |a Li, Min  |e verfasserin  |4 aut 
700 1 |a Wang, Shifu  |e verfasserin  |4 aut 
700 1 |a Guo, Han  |e verfasserin  |4 aut 
700 1 |a Hu, Ruanbo  |e verfasserin  |4 aut 
700 1 |a Tu, Kun-Hua  |e verfasserin  |4 aut 
700 1 |a Zhu, Wei  |e verfasserin  |4 aut 
700 1 |a Li, Xuning  |e verfasserin  |4 aut 
700 1 |a Yang, Xuan  |e verfasserin  |4 aut 
700 1 |a Pan, Yuan  |e verfasserin  |4 aut 
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773 1 8 |g volume:36  |g year:2024  |g number:11  |g day:01  |g month:03  |g pages:e2308243 
856 4 0 |u http://dx.doi.org/10.1002/adma.202308243  |3 Volltext 
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