Construction of Fe nanoclusters/nanoparticles to engineer FeN4 sites on multichannel porous carbon fibers for boosting oxygen reduction reaction

• Main Authors: Wang, Zhe, Lu, Zhe, Ye, Qitong, Yang, Zhenbei, Xu, Ruojie, Kong, Kexin, Zhang, Yifan, Yan, Tao, Liu, Yipu, Pan, Zhijuan, Huang, Yizhong, Lu, Xuehong
• Other Authors: School of Materials Science and Engineering
• Format: Article
• Language: English
• Published: 2024
• Subjects: Engineering; Carbon fiber; Nanocluster
• Online Access: https://hdl.handle.net/10356/176228
• Institution: Nanyang Technological University

Fe–N–C catalysts are emerging as promising alternatives to Pt-based catalysts for the oxygen reduction reaction (ORR), while they still suffer from sluggish reaction kinetics due to the discontented binding affinity between the Fe-N4 sites and oxygen-containing intermediates, and unsatisfactory stability. Herein, a flexible multichannel carbon fiber membrane immobilized with atomically dispersed Fe-N4 sites and neighboring Fe nanoclusters/nanoparticles (FeN4-FeNCP@MCF) is synthesized. The optimized geometric and electronic structures of the Fe atomic sites brought by adjacent Fe nanoclusters/nanoparticles and hierarchically porous structure of the carbon matrix endow FeN4-FeNCP@MCF with outstanding ORR activity and stability, considerably outperforming its counterpart with FeN4 sites only and the commercial Pt/C catalyst. Liquid and solid-state flexible zinc–air batteries employing FeN4-FeNCP@MCF both exhibit outstanding durability. Theoretical calculation reveals that the Fe nanoclusters can trigger remarkable electron redistribution of the FeN4 sites and modulate the hybridization of central Fe 3d and O 2p orbitals, facilitating the activation of O2 molecules and optimizing the adsorption capacity of oxygen-containing intermediates on FeN4 sites, and thus accelerating the ORR kinetic. This work offers an effective approach to constructing coupling catalysts that have single atoms coexisting with nanoclusters/nanoparticles for efficient ORR catalysis.