催化作用
化学气相沉积
无机化学
化学工程
材料科学
甲醇
化学
硫黄
碳纤维
铂金
金属
纳米技术
有机化学
复合数
冶金
复合材料
工程类
作者
Xiaohang Li,Xiaoxuan Yang,Liting Liu,He Zhao,Yawei Li,Haiyan Zhu,Yuanzhen Chen,Shengwu Guo,Yongning Liu,Qiang Tan,Gang Wu
标识
DOI:10.1021/acscatal.0c05446
摘要
Single metal site catalysts are the most promising candidates to replace platinum-group-metal (PGM) catalysts for the oxygen reduction reaction (ORR), yet insufficient performance and scalable preparation approaches remain great challenges. Here, we report a nitrogen (N)/sulfur (S) codoped single Fe site catalyst (Fe–N/S–C) through a chemical vapor deposition (CVD) strategy. Using the cyclopentadiene-shielded Fe atom ferrocene (Fc) as the precursor, atomically dispersed single Fe sites were successfully embedded into the N, S codoped 2D carbon nanosheets. The superior catalytic activity for the ORR in alkaline media is stemmed from the N, S codoping, tuning the optimal charge distribution of Fe sites. In addition, the CVD approach could surpress the formation of iron-carbide-containing iron clusters ("FexC/Fe"), thereby leading to high surface areas and porosity. Furthermore, the Fe–N/S–C catalyst was further studied as a cathode catalyst in direct methanol fuel cells showing encouraging performance.
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