ORR on highly-graphic mesoporous carbon-supported iron phthalocyanine in alkaline media
Jiang LH(姜鲁华) ; Qi J(齐静) ; Sun GQ(孙公权)
2010-09-26
会议名称61th annual meetiing of the international society of electrochemistry
会议日期2010-9-26
会议地点法国
页码无页码/2
通讯作者姜鲁华 ; 孙公权
中文摘要oxygen reduction reaction (orr) attracted extensive interests due to its importance in fuel cells. platinum is well known the best catalyst for the orr; however, several reasons limited the use of pt as the orr catalyst. first of all, pt is expensive due to its limitation in the earth. secondly, pt is easily poisoned by co which exists in reformed gases or by the intermediates from alcohol (crossover from anode for direct alcohol fuel cells) electrooxidation on cathode. therefore, it is necessary to explore non-noble metal electrocatalysts for orr. in this work, we deposited iron phthalocyanine (fepc) on different carbon supports, including vulcan xc72, black pearl, ketjin, and also homemade highly-graphic mesoporous carbon (hgmc) to produce carbon-supported fepc catalysts. the physical properties of the catalysts were characterized by xrd and tem. the activity and stability of these catalysts towards the orr were investigated in alkaline media. the mechanism and kinetics of the orr on the carbon-supported fepc catalysts will be discussed. anion-exchanged membrane fuel cell performances with the carbon-supported fepc as the cathode catalyst will be displayed. the relationship between the surface structure of the carbon-supported fepc catalysts and their activities will be discussed based on both the experimental results and dft simulations.
会议主办者elsevier
学科主题物理化学
语种中文
内容类型会议论文
源URL[http://159.226.238.44/handle/321008/114310]  
专题大连化学物理研究所_中国科学院大连化学物理研究所
推荐引用方式
GB/T 7714
Jiang LH,Qi J,Sun GQ. ORR on highly-graphic mesoporous carbon-supported iron phthalocyanine in alkaline media[C]. 见:61th annual meetiing of the international society of electrochemistry. 法国. 2010-9-26.
个性服务
查看访问统计
相关权益政策
暂无数据
收藏/分享
所有评论 (0)
暂无评论
 

除非特别说明,本系统中所有内容都受版权保护,并保留所有权利。


©版权所有 ©2017 CSpace - Powered by CSpace