聚苯胺
热解
材料科学
气凝胶
化学工程
空格(标点符号)
多孔介质
活性炭
多孔性
介孔材料
比表面积
碳纤维
氧还原
微型多孔材料
吸附
复合材料
聚合物
聚合
计算机科学
废物管理
工程类
复合数
操作系统
作者
Weiyu Zhang,Xiaocheng Xu,Chenxing Zhang,Zihuan Yu,Yiming Zhou,Yawen Tang,Ping Wu,Shaojun Guo
出处
期刊:Small methods
[Wiley]
日期:2017-07-18
卷期号:1 (8): 1700167-1700167
被引量:91
标识
DOI:10.1002/smtd.201700167
摘要
Iron and nitrogen co-doped carbon (Fe–N/C) nanomaterials are promising non-Pt catalysts toward the oxygen reduction reaction (ORR). Both spectroscopy and density functional theory studies reveal that Fe–Nx accounts for the ORR activity. However, Fe–N/C catalysts prepared by traditional high-temperature pyrolysis always contain less active Fe or Fe3C nanoparticles, and it remains a great challenge to obtain Fe–N/C catalysts with high-content Fe–Nx active sites. Herein, a 3D space-confined strategy for the pyrolysis of double-network aerogels is reported, to obtain Fe–N/C network catalysts with exclusive Fe–Nx active sites without the generation of Fe or Fe3C nanoparticles. The as-prepared Fe–N/C network exhibits more positive half-wave potential, higher diffusion-limited current density, and better selectivity for the ORR than catalysts derived from single aerogels and commercial Pt/C. Additionally, the ORR activity measured in potassium thiocyanate (KSCN) poisoned electrolyte corroborates that Fe–Nx is the active site. This work opens a new guideline for designing the M–N/C catalysts with exclusive active sites in porous carbon matrices for boosting energy electrocatalysis.
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