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Co- and defect-rich carbon nanofiber films as a highly efficient electrocatalyst for oxygen reduction
- Source :
- Applied Surface Science. 435:1159-1167
- Publication Year :
- 2018
- Publisher :
- Elsevier BV, 2018.
-
Abstract
- Many efforts are continuously devoted to developing high-efficiency, low-cost, and highly scalable oxygen reduction reaction (ORR) electrocatalysts to replace precious metal catalysts. Herein, we successfully synthesize Co- and defect-rich carbon nanofibers (CNFs) using an efficient heat treatment approach involving the pyrolysis of electrospun fibers at 370 °C under air. The heat treatment process produces Co-decorated CNFs with a high Co mass ratio, enriched pyridinic N, Co-pyridinic Nx clusters, and defect-rich carbon structures. The synergistic effects from composition and structural changes in the designed material increase the number of catalytically active sites for the ORR in an alkaline solution. The prepared Co- and defect-rich CNFs exhibit excellent ORR activities with a high ORR onset potential (0.954 V vs. RHE), a large reduction current density (4.426 mA cm−2 at 0.40 V), and a nearly four-electron pathway. The catalyst also exhibits a better long-term durability than commercial Pt/C catalysts. This study provides a novel hybrid material as an efficient ORR catalyst and important insight into the design strategy for CNF-based hybrid materials as electrochemical electrodes.
- Subjects :
- Materials science
Carbon nanofiber
General Physics and Astronomy
chemistry.chemical_element
02 engineering and technology
Surfaces and Interfaces
General Chemistry
010402 general chemistry
021001 nanoscience & nanotechnology
Condensed Matter Physics
Electrocatalyst
Electrochemistry
01 natural sciences
0104 chemical sciences
Surfaces, Coatings and Films
Catalysis
chemistry
Chemical engineering
0210 nano-technology
Hybrid material
Carbon
Cobalt
Pyrolysis
Subjects
Details
- ISSN :
- 01694332
- Volume :
- 435
- Database :
- OpenAIRE
- Journal :
- Applied Surface Science
- Accession number :
- edsair.doi...........8942620897a8ab8d1a15841f4f46ef1d
- Full Text :
- https://doi.org/10.1016/j.apsusc.2017.11.228