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Palladium phosphide nanoparticles embedded in 3D N, P co-doped carbon film for high-efficiency oxygen reduction
Seeking economical, efficient and stable catalysts to ameliorate the slow kinetics of oxygen reduction in cathode of proton exchange membrane fuel cells is still a great challenge. Herein, we design and synthesize an advanced Pd-based catalyst, where small palladium-phosphorus nanoparticles (Pd 3 P...
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Published in: | Journal of materials science 2021-06, Vol.56 (17), p.10523-10536 |
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Main Authors: | , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | Seeking economical, efficient and stable catalysts to ameliorate the slow kinetics of oxygen reduction in cathode of proton exchange membrane fuel cells is still a great challenge. Herein, we design and synthesize an advanced Pd-based catalyst, where small palladium-phosphorus nanoparticles (Pd
3
P NPs) with ~ 5.2 wt% Pd loading are embedded in three-dimensional (3D) bubble-like nitrogen, phosphorus co-doped carbon (NPC) film (Pd
3
P@NPC). The resultant catalyst delivers markedly enhancive catalytic performance in comparison with commercial Pt/C, Pd/C, Pd
3
P and NPC toward ORR, benefiting from the specific 3D porous structure, nano-size effect and the electronic interaction between Pd
3
P NPs and NPC. Specifically, the half-wave potential of Pd
3
P@NPC (0.885 V) is 36 mV higher than that of commercial Pt/C, and the mass activity of Pd
3
P@NPC is 1.112 mA
μ
g
Pd
-
1
at 0.85 V, which is 8.18-fold and 11.96-fold enhancement in regard to that of commercial Pt/C and Pd/C, respectively. It is interesting to note that the as-prepared Pd
3
P@NPC also maintains a predominant stability after 40,000 potential sweeping cycles. This new catalyst is expected to enlarge the species of 3D Pd-based composites such as palladium carbide, palladium nitride and palladium sulfide on heteroatoms doped carbon substrate for ORR. |
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ISSN: | 0022-2461 1573-4803 |
DOI: | 10.1007/s10853-021-05935-w |