Phosphonate-derived nitrogen-doped cobalt phosphate/carbon nanotube hybrids as highly active oxygen reduction reaction electrocatalysts

被引:34
|
作者
Zhao, Hui [1 ,2 ]
Weng, Chen-Chen [1 ]
Ren, Jin-Tao [1 ]
Ge, Li [1 ]
Liu, Yu-Ping [3 ]
Yuan, Zhong-Yong [1 ,3 ]
机构
[1] Nankai Univ, Sch Mat Sci & Engn, Natl Inst Adv Mat, Tianjin 300350, Peoples R China
[2] Liaocheng Univ, Sch Mat Sci & Engn, Liaocheng 252000, Shandong, Peoples R China
[3] Nankai Univ, Coll Chem, Minist Educ, Key Lab Adv Energy Mat Chem, Tianjin 300071, Peoples R China
基金
中国国家自然科学基金;
关键词
Metal phosphonate; Metal phosphate; Carbon nanotubes; Oxygen reduction reaction; Electrocatalysis; METAL-ORGANIC FRAMEWORKS; CARBON NANOTUBES; GRAPHENE; CATALYST; EVOLUTION; EFFICIENCY; OXIDATION; OXIDE;
D O I
10.1016/S1872-2067(19)63455-8
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
The exploration of cost-effective non-noble-metal electrocatalysts is highly imperative to replace the state-of-the-art platinum-based catalysts for oxygen reduction reaction (ORR). Here, we prepared cobalt phosphonate-derived N-doped cobalt phosphate/carbon nanotube hybrids (CoP-iC-N/CNTs) by hydrothermal treatment of N-containing cobalt phosphonate and oxidized carbon nanotubes (o-CNT) followed by high-temperature calcination under nitrogen atmosphere. The resultant CoPiC-N/CNT exhibits a superior electrocatalytic performance for the ORR in alkaline media, which is equal to the commercial Pt/C catalyst in the aspect of half-wave potential, onset potential and diffuse limiting current density. Furthermore, the excellent tolerance to methanol and strong durability outperform those of commercial Pt/C. It is found that cobalt phosphonate-derived N-doped cobalt phosphate and the in-situ formed graphitic carbons play key roles on the activity enhancement. Besides, introducing a suitable amount of CNTs enhances the electronic conductivity and further contributes to the improved ORR performance. (C) 2020, Dalian Institute of Chemical Physics, Chinese Academy of Sciences. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:259 / 267
页数:9
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