A Ni/Fe complex incorporated into a covalent organic framework as a single-site heterogeneous catalyst for efficient oxygen evolution reaction

被引:31
|
作者
Feng, Xuefeng [1 ,2 ]
Gao, Zhi [1 ,2 ]
Xiao, Longhui [1 ,2 ]
Lai, Zhenqin [1 ,2 ]
Luo, Feng [1 ,2 ,3 ]
机构
[1] East China Univ Technol, State Key Lab Nucl Resources & Environm, Nanchang 344000, Jiangxi, Peoples R China
[2] East China Univ Technol, Sch Biol Chem & Mat Sci, Nanchang 344000, Jiangxi, Peoples R China
[3] China Three Gorges Univ, Key Lab Inorgan Nonmetall Crystalline & Energy Co, Yichang 443002, Peoples R China
关键词
ELECTROCATALYSTS; OXIDATION; HYDROXIDE;
D O I
10.1039/d0qi00620c
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
A molecular NiFe complex (Cyclen@Ni0.5Fe0.5) was incorporated into the framework of COF (NH4@COF-SO3) by a one-pot post-synthesis method. The use of cyclen that can strongly chelate metal ions enables the formation of completely isolated metal sits uniformly distributed on the framework of COF. The resulting single-site heterogeneous catalyst ((Cyclen@Ni0.5Fe0.5)@COF-SO3) exhibits outstanding oxygen evolution reaction (OER) activity because of the maximum atom-utilization efficiency and significant bimetallic synergy effect. The TOF value at the overpotential of 300 mV reaches as high as 0.69 s(-1), which is superior to most of the recently reported efficient OER electrocatalysts. Moreover, the catalyst is stable and reusable without the loss of current density during a 25 h long-term test. The combination of advantages of molecular catalysts (metal complex) similar to homogeneous catalysts and solid COF materials for the fabrication of single-site heterogeneous catalysts first reported in this work can bring new avenues to develop highly efficient and stable COF-based catalysts in different catalytic fields.
引用
收藏
页码:3925 / 3931
页数:7
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