Promoting oxygen reduction via crafting bridge-bonded oxygen ligands on a single-atom iron catalyst. Issue 13 (31st May 2022)

• Record Type: Journal Article
• Authors: Xu, Chuanlan; Si, Yujun; Hu, Bingbing; Xu, Xinru; Hu, Bihao; Jiang, Ying; Chen, Haifeng; Guo, Chaozhong; Li, Honglin; Chen, Changguo
• Is Part Of: Inorganic chemistry frontiers. Volume 9:Issue 13(2022)
• Page Start: 3306
• Page End: 3318
• Publication Date: 2022-05-31
• Subjects: Chemistry, Inorganic -- Periodicals; 546.05
• DOI: 10.1039/d2qi00668e
• Languages: English
• ISSNs: 2052-1553

Abstract

Abstract : A bonding confinement strategy was used to anchor FePc molecules on a pre-synthesized Fe–N–C material with axially coordinated O-FeN4 sites. The O-FeN4 sites can improve charge transfer and promote ORR activity. Abstract : Single-atom Fe–N–C materials with Fe–N4 coordination structures, hailed as promising catalysts, are prohibited by the severe aggregation and migration of metal atoms. Although bonding-confinement strategies can be used to effectively regulate and strengthen the coordination of isolated metal atoms, the precise control of the coordination environment of metal centers remains a challenge. Herein, we report a rational strategy by which to bond iron phthalocyanine (FePc) on pre-synthesized Fe–N–C materials to further obtain anatomically dispersed Fe–N4 catalysts. The axial coordination of O-FeN4 sites to form a Fe–O–Fe bridge bond lowers the overpotential for the oxygen reduction reaction (ORR). Incorporation of the O atom stimulates the adsorbed O2 to obtain more electrons, thereby enhancing the adsorption and activation of O2 . The catalyst demonstrates a half-wave potential of 0.866 V ( versus RHE) and kinetic current density of 11.49 mA cm −2, significantly outperforming commercial Pt/C. The primary Zn–air battery assembled with such a catalyst exhibits a high current density of 136 mA cm −2 @ 1.0 V and a maximum power density of 205 mW cm −2, supporting its potential feasibility in practical applications. Our findings provide a new avenue for tuning the coordination environment of single-atom catalysts to enhance their ORR activity.