Increasing Accessible Active Site Density of Non-Precious Metal Oxygen Reduction Reaction Catalysts through Ionic Liquid Modification

被引:18
作者
Zhang, Gui-Rong [1 ,2 ]
Yong, Cong [1 ]
Shen, Liu-Liu [1 ,2 ]
Yu, Hui [1 ]
Brunnengraeber, Kai [2 ]
Imhof, Timo [2 ]
Mei, Donghai [1 ,3 ]
Etzold, Bastian J. M. [2 ]
机构
[1] Tiangong Univ, Sch Chem Engn & Technol, Tianjin 300387, Peoples R China
[2] Tech Univ Darmstadt, Ernst Berl Inst Tech & Makromol Chem, Dept Chem, D-64287 Darmstadt, Germany
[3] Tiangong Univ, Sch Environm Sci & Engn, Tianjin 300387, Peoples R China
基金
中国国家自然科学基金; 欧洲研究理事会;
关键词
non-precious metal catalysts; oxygen reduction reaction; ionic liquids; ZIF-derived carbon; electrochemically active surface area; N-C CATALYSTS; PERFORMANCE; ELECTROCATALYSTS; WATER; TEMPERATURE; CARBONS; CELL; ADSORPTION; IRON;
D O I
10.1021/acsami.2c21441
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Non-precious metal catalysts show great promise to replace the state-of-the-art Pt-based catalysts for catalyzing the oxygen reduction reaction (ORR), while their catalytic activity still needs to be greatly improved before their broad-based application. Here, we report a facile approach to improving the performance of zeolitic imidazolate framework-derived carbon (ZDC) toward the ORR by incorporating a small amount of ionic liquid (IL). The IL would preferentially fill the micropores of ZDC and greatly enhance the utilization of the active sites within the micropores, which are initially not accessible due to insufficient surface wetting. It is also disclosed that the ORR activity in terms of kinetic current at 0.85 V depends on the loading amount of the IL, and the maximum activity is obtained at a mass ratio of IL to ZDC at 1.2. The optimum stems from the counterbalance between the enhanced utilization of the active sites within the micropores and the retarded diffusion of the reactants within the IL phase due to its high viscosity.
引用
收藏
页码:18781 / 18789
页数:9
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