Boosting Oxygen Reduction of Single Iron Active Sites via Geometric and Electronic Engineering: Nitrogen and Phosphorus Dual Coordination

• Published in: Journal of the American Chemical Society Vol. 142; no. 5; pp. 2404 - 2412
• Main Authors: Yuan, Kai, Lützenkirchen-Hecht, Dirk, Li, Longbin, Shuai, Ling, Li, Yizhe, Cao, Rui, Qiu, Ming, Zhuang, Xiaodong, Leung, Michael K. H, Chen, Yiwang, Scherf, Ullrich
• Format: Journal Article
• Language: English
• Published: United States American Chemical Society 05.02.2020; American Chemical Society (ACS)
• Subjects: active sites; adsorption; Batteries; carbon; Catalysts; catalytic activity; cobalt; copper; desorption; engineering; geometry; INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CHEMISTRY; Iron; manganese; Materials; nanosheets; nickel; nitrogen; oxygen; phosphorus; reaction kinetics; Redox reactions
• ISSN: 0002-7863; 1520-5126; 1520-5126
• DOI: 10.1021/jacs.9b11852

Atomically dispersed transition metal active sites have emerged as one of the most important fields of study because they display promising performance in catalysis and have the potential to serve as ideal models for fundamental understanding. However, both the preparation and determination of such active sites remain a challenge. The structural engineering of carbon- and nitrogen-coordinated metal sites (M–N–C, M = Fe, Co, Ni, Mn, Cu, etc.) via employing new heteroatoms, e.g., P and S, remains challenging. In this study, carbon nanosheets embedded with nitrogen and phosphorus dual-coordinated iron active sites (denoted as Fe-N/P-C) were developed and determined using cutting edge techniques. Both experimental and theoretical results suggested that the N and P dual-coordinated iron sites were favorable for oxygen intermediate adsorption/desorption, resulting in accelerated reaction kinetics and promising catalytic oxygen reduction activity. This work not only provides efficient way to prepare well-defined single-atom active sites to boost catalytic performance but also paves the way to identify the dual-coordinated single metal atom sites.