Exploring the structural dependence of metal-free carbon electrocatalysts on zinc-based metal-organic framework types

被引:6
|
作者
Si, Wenfang [1 ]
Xie, Qianjie [1 ]
Zhang, Ruiyi [1 ]
Wang, Zheng [2 ]
Shen, Yehua [1 ]
Uyama, Hiroshi [3 ]
机构
[1] Northwest Univ, Key Lab Synthet & Nat Funct Mol Chem, Minist Educ, Coll Chem & Mat Sci, 1 Xuefu Rd, Xian 710127, Shaanxi, Peoples R China
[2] Northwest Univ, Coll Food Sci & Engn, 229 Taibai North Rd, Xian 710069, Shaanxi, Peoples R China
[3] Osaka Univ, Grad Sch Engn, Dept Appl Chem, Suita, Osaka 5650871, Japan
关键词
NITROGEN-DOPED CARBON; OXYGEN REDUCTION; HYDROGEN EVOLUTION; GRAPHITIC-N; NANOTUBES; MOF-5; CATALYST; OXIDE;
D O I
10.1039/d2dt01718k
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Metal-organic frameworks (MOFs) have been widely used as precursors to derive carbon-based electrocatalysts for the oxygen reduction reaction (ORR) due to their high porosity and tunable chemical composition/structure. However, the influence of MOF type on the structure and further ORR activity of derived metal-free carbon catalysts is still elusive. In the present work, a series of different Zn-based MOFs were employed as precursors to explore this issue. Meanwhile, prepare N-doped metal-free carbon catalysts were prepared for the ORR under the activation of sacrificial urea (which is effective to enhance the ORR activity of carbon-based catalysts). By analyzing the intermediates during pyrolysis, it is found that the decisive role of MOF types on the doped N and the morphology of derived carbon catalysts was played by the Zn coordination environment of MOFs and its reactivity with the decomposition intermediate of urea. Although the structure and porosity of derived carbon catalysts from different MOFs are very different, they all showed superior ORR activity and Zn-air battery performance up to 20 wt% Pt/C benchmark catalysts. From the above analyses, the combination of urea and compounded Zn is also a promising activation method for the preparation of highly-efficient metal-free carbon electrocatalysts.
引用
收藏
页码:11363 / 11371
页数:9
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