Co 2 B and Co Nanoparticles Immobilized on the N-B-Doped Carbon Derived from Nano-B 4 C for Efficient Catalysis of Oxygen Evolution, Hydrogen Evolution, and Oxygen Reduction Reactions
A novel hybrid electrocatalyst of Co B and Co nanoparticles immobilized on N-B-doped carbon derived from nano-B C (Co B/Co/N-B-C/B C) is in situ synthesized by pyrolysis of nano-B C supporting Co(OH) nanoparticles with melamine. The Co B and Co nanoparticles are formed and anchored on the generated...
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Veröffentlicht in: | ACS applied materials & interfaces 2018-10, Vol.10 (43), p.37067-37078 |
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Hauptverfasser: | , , , , , , , |
Format: | Artikel |
Sprache: | eng |
Online-Zugang: | Volltext |
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Zusammenfassung: | A novel hybrid electrocatalyst of Co
B and Co nanoparticles immobilized on N-B-doped carbon derived from nano-B
C (Co
B/Co/N-B-C/B
C) is in situ synthesized by pyrolysis of nano-B
C supporting Co(OH)
nanoparticles with melamine. The Co
B and Co nanoparticles are formed and anchored on the generated N and B codoped carbon and undecomposed B
C. The hybrid exhibits remarkable catalytic performances toward the oxygen evolution reaction (OER) and oxygen reduction reaction (ORR)-a very small potential of 1.53 V at 10 mA cm
for the OER and a high catalytic kinetics and superior durability for the ORR-which are superior to the RuO
and Pt/C catalyst, respectively. Most impressively, the hybrid delivers a very small potential gap of 710 mV, which is lower than those of most bifunctional electrocatalysts reported. In addition, the hybrid also shows a satisfying hydrogen evolution reaction performance offering a small overpotential of 220 mV at 10 mA cm
and wonderful stability. The excellent trifunctional catalytic performances issue from synergetic effects of Co
B, metal Co, Co/N-doped carbon, and B self-doped carbon coexisting in the hybrid with good interaction mutually. This work provides a new-type efficient multifunctional catalyst for regenerative fuel cell and overall water-splitting technologies. |
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ISSN: | 1944-8244 1944-8252 |
DOI: | 10.1021/acsami.8b13359 |