Composite Electrocatalyst Derived from Hybrid Nitrogen-Containing Metal Organic Frameworks and g-C3N4 Encapsulated InSitu into Porous Carbon Aerogels

被引:9
作者
Zhu, Hong [1 ]
Chen, Minglin [1 ]
Li, Ke [1 ]
Huang, Xidai [1 ]
Wang, Fanghui [1 ]
机构
[1] Beijing Univ Chem Technol, Sch Sci, Dept Organ Chem, Inst Modern Catalysis,State Key Lab Chem Resource, Beijing 100029, Peoples R China
基金
中国国家自然科学基金;
关键词
metal organic framework; graphitic C3N4; porous carbon aerogel; non-precious metal catalysts; oxygen reduction reaction; OXYGEN REDUCTION REACTION; TEMPLATE-FREE SYNTHESIS; DOPED CARBON; RECENT PROGRESS; CATALYSTS; ALKALINE; NANOSTRUCTURES; GRAPHENE; PERFORMANCE; STABILITY;
D O I
10.1002/celc.201800479
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
A novel composite Fe-bpdc-C3N4-CA catalyst (where bpdc stands for 2,2'-bipyridine-3,3'-dicarboxylic acid and CA stands for carbon aerogel) with a high nitrogen content was synthesized through the insitu encapsulation of nitrogen-containing metal organic frameworks along with g-C3N4 into porous CAs. The characteristics of the catalysts calcined at different temperatures were determined by means of TEM, XRD, Raman spectroscopy, XPS, and BET measurements. The results demonstrate the successful doping of N heteroatoms and the effective formation of Fe-N-X active sites. The electrocatalytic properties were investigated by using rotating disk electrode (RDE) and rotating ring disk electrode (RRDE) measurements. The Fe-bpdc-C3N4-CA catalyst calcined at 800 degrees C exhibits the highest oxygen reduction reaction activity with the initial reduction potential and half-wave potential reaching 1.09 and 0.96V, respectively, versus RHE in 0.1M KOH. It also possesses high stability and follows approximately a complete four-electron (4e(-)) reaction pathway, as commercial Pt/C catalysts do.
引用
收藏
页码:2126 / 2134
页数:9
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