Effect of pyrolysis conditions on nitrogen-doped ordered mesoporous carbon electrocatalysts

热解 材料科学 介孔材料 电催化剂 化学工程 碳纤维 X射线光电子能谱 比表面积 解吸 循环伏安法 催化作用 无机化学 吸附 电化学 化学 电极 有机化学 复合材料 物理化学 复合数 工程类
作者
Guifa Long,Kai Wan,Mingyao Liu,Xiaohua Li,Zhenxing Liang,Jinhua Piao
出处
期刊:Chinese Journal of Catalysis [Elsevier BV]
卷期号:36 (8): 1197-1204 被引量:34
标识
DOI:10.1016/s1872-2067(15)60912-3
摘要

Pt is the most effective and widely used electrocatalyst for the oxygen reduction reaction (ORR) in fuel cells; however, its scarcity and high cost pose a great challenge to the commercialization of the fuel cell technology. N-doped carbon materials have been regarded as one of the most promising Pt-alternative catalysts. In this work, the N-doped ordered mesoporous carbon was synthesized by the nanocasting method using SBA-15 as the template. The effect of the pyrolysis conditions (pyrolysis temperature, pyrolysis duration, and ramp rate) on this material was investigated. N2 adsorption-desorption isotherms, X-ray photoelectron spectroscopy, and Raman spectroscopy were used to investigate the intrinsic properties of the resultant materials. Cyclic voltammetry and rotating ring-disk electrode were used to investigate the electrochemical behavior for ORR in an alkaline medium. It was found that the resultant mesoporous carbon materials exhibit high electrical conductivity, high specific surface area, and unique pore structure. The pyrolysis temperature was the most important parameter in determining the thermodecomposition of the carbon precursor, and the microstructure, elemental composition, and chemical configuration of the resultant mesoporous carbon materials. To achieve reasonable electrocatalytic activity and selectivity, a high pyrolysis temperature above 800 °C is required for effective N doping to form active sites and for graphitization to facilitate charge transfer, whereas the pyrolysis duration and ramp rate have a much less significant effect. This indicates that both the surface composition/structure and consequent electrochemical properties are more dependent on the thermodynamics than the kinetics during the pyrolysis process. Finally, the optimal N-doped ordered mesoporous carbon catalyst showed superior electrochemical activity for ORR than the commercial Pt catalyst and is promising for fuel cell and metal–air battery applications.
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