电催化剂
双金属片
催化作用
石墨氮化碳
石墨烯
甲醇
氧化物
钴
材料科学
无机化学
化学工程
甲醇燃料
化学
电解质
旋转圆盘电极
电化学
纳米技术
电极
循环伏安法
光催化
有机化学
物理化学
工程类
作者
Wan‐Kuen Jo,M. Satyanarayana,Dong‐Eun Lee,Surendar Tonda
标识
DOI:10.1016/j.apsusc.2020.147367
摘要
Abstract The electrocatalytic oxygen reduction reaction (ORR) in acidic media is quite strenuous. Although platinum (Pt)-based materials are considered state-of-the-art ORR catalysts, their high cost and poor durability greatly impede their extensive application in polymer electrolyte membrane fuel cells and direct methanol fuel cells. Here, we report a bimetallic M–Nx–C-class electrocatalyst comprising Co- and Fe-coordinated graphitic carbon nitride ((Co,Fe)–CN) and reduced graphene oxide (RGO) as an effective substitute for expensive Pt-based catalysts for the ORR in acidic media. The fabricated (Co,Fe)–CN/RGO catalyst exhibits a high surface area, high porosity, fast charge-transfer kinetics at the (Co,Fe)–CN/RGO 2D/2D interface, and abundant Co–Nx–C and Fe–Nx–C active sites. Because of these favorable properties, the optimized (Co,Fe)–CN/RGO catalyst displayed extraordinary electrocatalytic ORR activity, with an onset potential of 875 mV, which is only 41 mV more negative than that of a commercial Pt/C, and follows an efficient four-electron reaction pathway in acidic media. Notably, the fabricated catalyst demonstrated excellent methanol tolerance and long-term stability compared with the reference Pt/C. Therefore, this work provides a rational design approach to fabricating graphitic-C3N4-based nonprecious bimetallic electrocatalysts with M–Nx–C active sites for enhanced ORR activity in fuel-cell applications.
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