Issue 113, 2015

Hybrids based on transition metal phosphide (Mn2P, Co2P, Ni2P) nanoparticles and heteroatom-doped carbon nanotubes for efficient oxygen reduction reaction

Abstract

Hybrids based on transition metal phosphide (Mn2P, Co2P, Ni2P) nanoparticles and heteroatom-doped carbon nanotubes were facilely synthesized, and used as efficient oxygen reduction reaction (ORR) catalysts in alkaline solution. Transition metal phosphide nanoparticles formed core/shell structures with graphitic carbon, and the nanoparticles (core) can significantly influence the ORR catalytic activity of the carbon shell. Hybrids based on Co2P and Mn2P decorated heteroatom-doped carbon exhibit excellent ORR catalytic activity with regards to dominant 4eāˆ’ process, low over potential, excellent methanol tolerance and durability. In contrast, Ni2P decorated heteroatom-doped carbon shows inferior ORR catalytic activity. The variation of ORR performance mainly derives from the collective effect of the electronegativity and binding energy shift of the transition metals, which would result in a different surface electronic structure of the heteroatom-doped carbon. Low electronegativity and low binding energy shift of the transition metals would lead to strong electron-donating ability of the transition metal phosphide nanoparticles, resulting in the enhanced ORR catalytic activity of the hybrid materials. This work is significant for development of advanced ORR catalysts based on heteroatom-doped carbon via rational design of the structure of hybrid materials.

Graphical abstract: Hybrids based on transition metal phosphide (Mn2P, Co2P, Ni2P) nanoparticles and heteroatom-doped carbon nanotubes for efficient oxygen reduction reaction

Supplementary files

Article information

Article type
Paper
Submitted
07 Aug 2015
Accepted
21 Oct 2015
First published
22 Oct 2015

RSC Adv., 2015,5, 92893-92898

Hybrids based on transition metal phosphide (Mn2P, Co2P, Ni2P) nanoparticles and heteroatom-doped carbon nanotubes for efficient oxygen reduction reaction

K. Chen, X. Huang, C. Wan and H. Liu, RSC Adv., 2015, 5, 92893 DOI: 10.1039/C5RA21385A

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