One-Step Synthesis of Supported High-Index Faceted Platinum–Cobalt Nanocatalysts for an Enhanced Oxygen Reduction Reaction
Source abstract
Abstract
The slow rate of the oxygen reduction reaction (ORR) is the main barrier limiting the commercialization of proton exchange membrane fuel cells on an industrial scale. Here, we report a one-step synthetic strategy of a class of carbon-supported Pt–Co alloy concave nanocubes (NCs) with {hk0} high-index facets with a high ORR activity. The concave degree of the Pt–Co alloy is tunable through adjusting the amount of short carbon-chain capping agent—n-butylamine. In the growth process, carbon black serves as a dispersant to avoid the nanoparticle aggregation and thus favor the generation of concave NCs in addition to the function as the support for Pt–Co nanoparticles. The carbon-supported Pt–Co concave NCs with 22% Pt–Co by weight deliver a specific activity of 2.34 mA cm–2 and mass activity of 0.26 A mg–1Pt toward ORR, representing 6.5-fold and twofold enhancement, respectively, relative to the state-of-the-art commercial Pt/C. After 5000 cycles of the accelerated durability test, the mass activity of carbon-supported Pt–Co concave NCs is still higher than that of pristine commercial Pt/C.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Electrocatalysts for Energy Conversion · Fuel Cells and Related Materials · Advanced battery technologies research
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
State Key Laboratory for Oxo Synthesis and Selective Oxidation, Suzhou Research Institute of LICP, Lanzhou Institute of Chemical Physics (LICP), Chinese Academy of Sciences, Lanzhou 730000, China
Funding
Natural Science Foundation of Jiangsu Province · National Natural Science Foundation of China
References (37)
Show source-provided references
1. 10.1016/j.apcatb.2004.06.02110.1016/j.apcatb.2004.06.021 ↗
2. 10.1016/j.nantod.2008.09.00210.1016/j.nantod.2008.09.002 ↗
3. 10.1038/nature1111510.1038/nature11115 ↗
4. 10.1021/jacs.5b1005910.1021/jacs.5b10059 ↗
5. 10.1038/nchem.36710.1038/nchem.367 ↗
6. 10.1126/science.117037710.1126/science.1170377 ↗
7. 10.1126/science.113594110.1126/science.1135941 ↗
8. 10.1021/ja303950v10.1021/ja303950v ↗
9. 10.1021/nl401881z10.1021/nl401881z ↗
10. 10.1126/science.124906110.1126/science.1249061 ↗
11. 10.1126/science.aaa876510.1126/science.aaa8765 ↗
12. 10.1038/ncomms1185010.1038/ncomms11850 ↗
13. 10.1126/science.aaw749310.1126/science.aaw7493 ↗
14. 10.1039/C6TA02202B10.1039/C6TA02202B ↗
15. 10.1002/anie.20141154410.1002/anie.201411544 ↗
16. 10.1126/sciadv.160170510.1126/sciadv.1601705 ↗
17. 10.1002/anie.20191030910.1002/anie.201910309 ↗
18. 10.1016/j.joule.2019.12.01410.1016/j.joule.2019.12.014 ↗
19. 10.1002/anie.20050438610.1002/anie.200504386 ↗
20. 10.1038/nchem.62310.1038/nchem.623 ↗
21. 10.1021/ja312382h10.1021/ja312382h ↗
22. 10.1021/nl501205j10.1021/nl501205j ↗
23. 10.1038/ncomms859410.1038/ncomms8594 ↗
24. 10.1021/acs.nanolett.7b0223910.1021/acs.nanolett.7b02239 ↗
25. 10.1002/anie.20080224810.1002/anie.200802248 ↗
26. 10.1021/ar200293n10.1021/ar200293n ↗
27. 10.1126/science.114048410.1126/science.1140484 ↗
28. 10.1002/anie.20110300210.1002/anie.201103002 ↗
29. 10.1002/anie.20140649710.1002/anie.201406497 ↗
30. 10.1039/C4NR00313F10.1039/C4NR00313F ↗
31. 10.1039/C6CS00039H10.1039/C6CS00039H ↗
32. 10.1093/nsr/nwv01410.1093/nsr/nwv014 ↗
33. 10.1016/j.nantod.2013.02.00610.1016/j.nantod.2013.02.006 ↗
34. 10.1021/ar300359w10.1021/ar300359w ↗
35. 10.1039/c2cc33126h10.1039/c2cc33126h ↗
36. 10.1016/j.scib.2017.05.02910.1016/j.scib.2017.05.029 ↗
37. 10.1021/ja413209q10.1021/ja413209q ↗