Hierarchically Porous Carbons with Highly Curved Surfaces for Hosting Single Metal FeN4 Sites as Outstanding Oxygen Reduction Catalysts

• Published in: Advanced materials (Weinheim) 2023-08, Vol.35 (32), p.e2300907-n/a
• Main Authors: Chen, Guangbo, Lu, Ruihu, Li, Chenzhao, Yu, Jianmin, Li, Xiaodong, Ni, Lingmei, Zhang, Qi, Zhu, Guangqi, Liu, Shengwen, Zhang, Jiaxu, Kramm, Ulrike I., Zhao, Yan, Wu, Gang, Xie, Jian, Feng, Xinliang
• Format: Article
• Language: English
• Subjects: Carbon; carbon curvature; Catalysis; Catalysts; Chemical reduction; Displays; Electrocatalysts; Electrodes; Fe–N–C catalysts; Fuel cells; hierarchically porous carbons; INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CHEMISTRY; Iron; Materials science; Membranes; Nitrogen; oxygen reduction reaction; Oxygen reduction reactions; Stability; Sulfuric acid
• ISSN: 0935-9648; 1521-4095
• DOI: 10.1002/adma.202300907

Iron–nitrogen–carbon (FeNC) materials have emerged as a promising alternative to platinum‐group metals for catalyzing the oxygen reduction reaction (ORR) in proton‐exchange‐membrane fuel cells. However, their low intrinsic activity and stability are major impediments. Herein, an FeN–C electrocatalyst with dense FeN4 sites on hierarchically porous carbons with highly curved surfaces (denoted as FeN4‐hcC) is reported. The FeN4‐hcC catalyst displays exceptional ORR activity in acidic media, with a high half‐wave potential of 0.85 V (versus reversible hydrogen electrode) in 0.5 m H2SO4. When integrated into a membrane electrode assembly, the corresponding cathode displays a high maximum peak power density of 0.592 W cm−2 and demonstrates operating durability over 30 000 cycles under harsh H2/air conditions, outperforming previously reported Fe–NC electrocatalysts. These experimental and theoretical studies suggest that the curved carbon support fine‐tunes the local coordination environment, lowers the energies of the Fe d‐band centers, and inhibits the adsorption of oxygenated species, which can enhance the ORR activity and stability. This work provides new insight into the carbon nanostructure–activity correlation for ORR catalysis. It also offers a new approach to designing advanced single‐metal‐site catalysts for energy‐conversion applications. The oxygen reduction reaction activity and stability of a single‐atom FeNC electrocatalyst are promoted by engineering FeN4 active sites on hierarchical carbons comprising highly curved surfaces (FeN4‐hcC). The achieved FeN4‐hcC displays outstanding oxygen reduction reaction performance in acidic media and promising activity in proton‐exchange‐membrane fuel cells.