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Highly efficient PtCo nanoparticles on Co–N–C nanorods with hierarchical pore structure for oxygen reduction reaction
Authors:Rongcheng Mo  Xiaoran Zhang  Zhenyu Chen  Shangli Huang  Yanjie Li  Lizhe Liang  Zhi Qun Tian  Pei Kang Shen
Affiliation:1. Collaborative Innovation Center of Sustainable Energy Materials, School of Physical Science and Technology, Guangxi University, Nanning, 530004, China;2. Guangxi Key Laboratory of Electrochemical Energy Materials, Nanning, 530004, China;3. Key Laboratory of New Processing Technology for Non-ferrous Metal and Materials, Ministry of Education, Nanning, 530004, China;4. School of Chemistry & Chemical Engineering, Guangxi University, Nanning, 530004, China
Abstract:Developing platinum-based nanoparticles on carbon catalysts with high activity and stability for oxygen reduction reaction (ORR) is of great significance for the practical application of fuel cells. Herein, a synchronous strategy of preparing nano-sized PtCo supported on atomic Co and N co-doped carbon nanorods (PtCo/Co–N–C NR) was developed to replace the conventional method of impregnating Pt sources into ready-made carbon materials, in which metal-organic frameworks (MOFs) with Co and Zn ions of rhombic dodecahedron were first prepared using 2-methylimidazole as building block and then their morphology was transformed into porous nanorods via the reduction of Co ions to Co–B–O complex in the MOFs by NaBH4; subsequently, Pt was deposited on the Co–Zn MOF nanorods through the displacement reaction of PtCl62- and metallic Co and coordination between MOF and PtCl62-; after pyrolysis and acid-leaching process, highly dispersed PtCo/Co–N–C NR was obtained. Attributed to its unique characteristics of hierarchical pore structure, uniform PtCo alloy nanoparticles with the average size of 7.0 nm and strong supporting interaction effect, the catalyst exhibits high ORR activity and stability with the mass activity of 577.0 mA mg?1Pt and specific activity of 1.4 mA cm?2 at 0.9 V vs RHE in 0.1 M HClO4, which is about 3.6 times and 3.5 times high than that of commercial Pt/C catalyst respectively. This strategy would provide a flexible route to develop highly active and stable ORR electrocatalysts with various morphologies for optimizing the exposure of active sites.
Keywords:Metal-organic frameworks  Co–N–C electrocatalyst  PtCo nanoparticles  Oxygen reduction reaction  Fuel cells
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