催化作用
化学气相沉积
质子交换膜燃料电池
电化学
金属
化学工程
铂金
氮气
碳纤维
电解质
材料科学
无机化学
化学
纳米技术
电极
有机化学
物理化学
工程类
复合数
复合材料
冶金
作者
Shengwen Liu,Maoyu Wang,Xiaoxuan Yang,Qiurong Shi,Zhi Qiao,Marcos Lucero,Qing Ma,Karren L. More,David A. Cullen,Zhenxing Feng,Gang Wu
标识
DOI:10.1002/anie.202009331
摘要
Atomically dispersed and nitrogen coordinated single metal sites (M-N-C, M=Fe, Co, Ni, Mn) are the popular platinum group-metal (PGM)-free catalysts for many electrochemical reactions. Traditional wet-chemistry catalyst synthesis often requires complex procedures with unsatisfied reproducibility and scalability. Here, we report a facile chemical vapor deposition (CVD) strategy to synthesize the promising M-N-C catalysts. The deposition of gaseous 2-methylimidazole onto M-doped ZnO substrates, followed by an in situ thermal activation, effectively generated single metal sites well dispersed into porous carbon. In particular, an optimal CVD-derived Fe-N-C catalyst exclusively contains atomically dispersed FeN4 sites with increased Fe loading relative to other catalysts from wet-chemistry synthesis. The catalyst exhibited outstanding oxygen-reduction activity in acidic electrolytes, which was further studied in proton-exchange membrane fuel cells with encouraging performance.
科研通智能强力驱动
Strongly Powered by AbleSci AI