A MnOx enhanced atomically dispersed iron–nitrogen–carbon catalyst for the oxygen reduction reaction. Issue 11 (17th November 2021)

• Record Type: Journal Article
• Authors: Ding, Shichao; Lyu, Zhaoyuan; Sarnello, Erik; Xu, Mingjie; Fang, Lingzhe; Tian, Hangyu; Karcher, Sam Ellery; Li, Tao; Pan, Xiaoqing; McCloy, John; Ding, Guodong; Zhang, Qiang; Shi, Qiurong; Du, Dan; Li, Jin-Cheng; Zhang, Xiao; Lin, Yuehe
• Is Part Of: Journal of materials chemistry. Volume 10:Issue 11(2022)
• Page Start: 5981
• Page End: 5989
• Publication Date: 2021-11-17
• Subjects: Materials -- Research -- Periodicals; Chemistry, Analytic -- Periodicals; Environmental sciences -- Research -- Periodicals; 543.0284
• DOI: 10.1039/d1ta07219f
• Languages: English
• ISSNs: 2050-7488

Abstract

Abstract : A MnO x -assisted strategy is proposed to improve the oxygen reduction activity and stability of Fe–N–C single-atom catalysts (SACs) by regulating the electron structure and reducing the side effects of the Fenton reaction. Abstract : Cost-effective and highly efficient Fe–N–C single-atom catalysts (SACs) have been considered to be one of the most promising potential Pt substitutes for the cathodic oxygen reduction reaction (ORR) in proton exchange membrane fuel cells (PEMFCs). Nevertheless, they are subject to severe oxidative corrosion originating from the Fenton reaction, leading to poor long-time durability of PEMFCs. Herein, we propose a MnO x engineered Fe–N–C SAC (Mn–Fe–N–C SAC) to reduce and even eliminate the stability issue, as MnO x accelerates the degradation of the H2 O2 by-product via a disproportionation reaction to weaken the Fenton reaction. As a result, the Mn–Fe–N–C SAC shows an ultralow H2 O2 yield and a negligible half-wave potential shift after 10 000 continuous potential cycles, demonstrating excellent ORR stability. Besides, the Mn–Fe–N–C SAC also shows an improved ORR activity compared to the common Fe–N–C SAC. Results show that the MnO x interacts with the Fe–N x site, possibly forming Fe–Mn or Fe–O–Mn bonds, and enhances the intrinsic activity of single iron sites. This work provides a method to overcome the stability problem of Fe–N–C SACs while still yielding excellent catalytic activity, thus showing great promise for application in PEMFCs.