青岛科技大学  English 
姜鲁华
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教师拼音名称:jiangluhua

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2023-09-01 山东省教书育人楷模

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Boosting Oxygen Reduction Reaction via N, S-Doped Carbon Shell-Encapsulated Fe<sub>5</sub>C<sub>2</sub>: Leveraging Lateral and Axial Synergy

关键字:ACTIVE-SITES; ELECTROCATALYSIS; PERFORMANCE; CATALYSTS

摘要:Herein, a novel oxygen reduction reaction (ORR) electrocatalyst, consisting of an N,S-codoped carbon shell encapsulating Fe5C2 nanoparticles, is developed through self-assembled supramolecular structures and controlled pyrolysis. The resulting Fe5C2@SNC catalyst exhibits exceptional electrocatalytic performance, with a high half-wave potential (E-1/2) of 0.86 V, comparable to that of commercial Pt/C. The distinctive core-shell structure contributes to excellent stability, demonstrating an 89% current maintenance after 20 h of continuous chronoamperometry testing. In Zn-air battery applications, the catalyst achieved a peak power density of 222 mW cm(-2), surpassing that of its Pt/C counterpart. Combining the experiments and density functional theory calculations, the synergistic effects of axial Fe5C2 nanoparticles and laterally SOx-functionalized Fe-N-x carbon planes within Fe5C2@SNC have been comprehensively unveiled. The electron-withdrawing nature of sulfur leads to charge redistribution, particularly on N sites proximal to the SOx group. Additionally, the axial Fe5C2 nanoparticles have precisely modulated the d-band center of the Fe5C2@SNC catalyst, optimizing oxygen intermediate adsorption and enhancing the ORR activity. This work highlights the understanding and harnessing of synergistic catalysis via a controllable core-shell structure, providing an effective way for developing highly efficient and stable electrocatalysts for energy conversion and storage applications.

卷号:12

期号:11

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