Carbon support tuned electrocatalytic activity of a single-site metal-organic framework toward the oxygen reduction reaction

被引:34
|
作者
Ma, Wenjie [1 ]
Wu, Fei [1 ]
Yu, Ping [1 ,3 ]
Mao, Lanqun [1 ,2 ]
机构
[1] Chinese Acad Sci, Beijing Natl Lab Mol Sci, Key Lab Analyt Chem Living Biosyst, Inst Chem, Beijing 100190, Peoples R China
[2] Beijing Normal Univ, Coll Chem, Xinjiekouwai St 19, Beijing 100875, Peoples R China
[3] Univ Chinese Acad Sci, Beijing 100049, Peoples R China
基金
中国国家自然科学基金;
关键词
66;
D O I
10.1039/d1sc00997d
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Metal-organic frameworks (MOFs) possess fantastic features such as structural diversity, tunable accessible pores and atomically dispersed active sites, holding tremendous potential as highly versatile platforms for fabricating single-site catalysts. The electrocatalytic activity of single-site MOFs can be improved and tuned via several approaches; however, the exploitation of different carbon supports to modulate the nature of single active sites in MOFs for electrocatalysis has not been reported. Here, we find that the electrocatalytic activity of single-site MOFs toward the oxygen reduction reaction (ORR) can be tuned by using carbon nanomaterials, i.e., carbon nanotubes and graphene, as supports through MOF-support interactions in the manner of geometric and electronic effects. The introduction of MOF-support interactions not only greatly improves the electrocatalytic performance of MOFs toward the ORR in terms of onset and half-wave potentials and current density, but also alters the reaction pathway of the ORR. This finding provides a new horizon for the design and synthesis of single-site MOFs for electrocatalysis.
引用
收藏
页码:7908 / 7917
页数:10
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