碳纤维
材料科学
金属
Atom(片上系统)
纳米技术
化学工程
催化作用
弧(几何)
电弧
闪光灯(摄影)
兴奋剂
电极
石墨烯
化学
复合数
光电子学
冶金
物理化学
有机化学
复合材料
光学
物理
工程类
嵌入式系统
计算机科学
数学
几何学
作者
Jae Young Jung,Jue‐Hyuk Jang,Jeong‐Gil Kim,Kug‐Seung Lee,Hyung‐Kyu Lim,Pil Kim,Robert P. H. Chang,Ji‐Woong Park,Sung Jong Yoo,Nam Dong Kim
出处
期刊:Small methods
[Wiley]
日期:2021-06-18
卷期号:5 (8): e2100239-e2100239
被引量:21
标识
DOI:10.1002/smtd.202100239
摘要
Abstract Despite considerable development in the field of single‐atom catalysts (SACs) on carbon‐based materials, the reported strategies for synthesizing SACs generally rely on top‐down approaches, which hinder achieving both simple and universal synthesis routes that are simultaneously applicable to various metals and nanocarbons. Here, a universal strategy for fabricating nanocarbon based‐SACs using a flash bottom‐up arc discharge method to mitigate these issues is reported. The ionization of elements and their recombination process during arc discharge allows the simultaneous incorporation of single metal atoms (Mn, Fe, Co, Ni, and Pt) into the crystalline carbon lattice during the formation of carbon nanohorns (CNHs) and N‐doped arc graphene. The coordination environment around the Co atoms of Co 1 /CNH can be modulated by a mild post‐treatment with NH 3 . As a result, Co 1 /CNH exhibits good oxygen reduction reaction activity, showing a 1.92 times higher kinetic current density value than the commercial Pt/C catalyst in alkaline media. In a single cell experiment, Co 1 /CNH exhibits the highest maximum power density of 472 mW cm −2 compared to previously reported nonprecious metal‐based SACs.
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