催化作用
电催化剂
热解
介孔材料
铜
材料科学
酞菁
碳纤维
化学
金属
无机化学
电化学
电极
核化学
纳米技术
复合数
物理化学
有机化学
复合材料
作者
Aoling Chen,Aiguo Kong,Xiaohong Fan,Xi Yang,Congling Li,Zhengyan Chen,Yongkui Shan
标识
DOI:10.1016/j.ijhydene.2017.05.188
摘要
The highly efficient Cu-based ORR catalysts (Cu–N–C) were obtained by the pyrolysis of mesoporous KIT-6 silica-supported phthalocyanines at superhigh temperature (1000 °C). The prepared Cu–N–C catalyst was demonstrated as one of the best Cu-based electrocatalysts for ORR, with 0.82 V half-wave potential in 0.1 M KOH and 0.72 V half-wave potential in 0.1 M HClO4. It showed the competitive ORR activity to high-performance Fe- or Co-based carbon catalysts. Moreover, the ORR catalytic performance of Cu–N–C could be further enhanced by co-doping few Fe species (Fe–Cu–N–C) into the carbon framework. It revealed about 30 mV higher half-wave potential and better stability than Cu–N–C catalyst in both alkaline and acidic media. Cu–N–C and Fe–Cu–N–C electrocatalysts could be produced at a scale of over 15 g by facilely enlarging the amount of phthalocyanine precursors. The high-efficiency ORR performance and scalable synthesis of Cu–N–C and Fe–Cu–N–C catalysts enabled them to be the potential substitutes to Pt-based electrocatalyst for ORR.
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