Surface-Limited Synthesis of Pt Nanocluster Decorated Pd Hierarchical Structures with Enhanced Electrocatalytic Activity toward Oxygen Reduction Reaction
Source abstract
Abstract
Exploring superior catalysts with high catalytic activity and durability is of significant for the development of an electrochemical device involving the oxygen reduction reaction. This work describes the synthesis of Pt-on-Pd bimetallic heterogeneous nanostructures, and their high electrocatalytic activity toward the oxygen reduction reaction (ORR). Pt nanoclusters with a size of 1-2 nm were generated on Pd nanorods (NRs) through a modified Cu underpotential deposition (UPD) process free of potential control and a subsequent surface-limited redox reaction. The Pt nanocluster decorated Pd nanostructure with a ultralow Pt content of 1.5 wt % exhibited a mass activity of 105.3 mA mg(-1) (Pt-Pd) toward ORR, comparable to that of the commercial Pt/C catalyst but 4 times higher than that of carbon supported Pd NRs. More importantly, the carbon supported Pt-on-Pd catalyst displays relatively small losses of 16% in electrochemical surface area (ECSA) and 32% in mass activity after 10 000 potential sweeps, in contrast to respective losses of 46 and 64% for the commercial Pt/C catalyst counterpart. The results demonstrated that Pt decoration might be an efficient way to improve the electrocatalytic activity of Pd and in turn allow Pd to be a promising substitution for commercial Pt catalyst.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Electrocatalysts for Energy Conversion · Machine Learning in Materials Science · Fuel Cells and Related Materials
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
School of Chemical Engineering, Huaihai Institute of Technology, Lianyungang 222005, People’s Republic of China
School of Materials Science and Engineering, Harbin University of Science and Technology, Harbin 150040, People’s Republic of China
Testing Center, Yangzhou University, Yangzhou, 225009, People’s Republic of China
Funding
National Natural Science Foundation of China · Lianyungang City
References (65)
Show source-provided references
1. 10.1016/j.apcatb.2004.06.02110.1016/j.apcatb.2004.06.021 ↗
2. 10.1016/j.jpowsour.2010.04.05210.1016/j.jpowsour.2010.04.052 ↗
3. 10.1038/nchem.103010.1038/nchem.1030 ↗
4. 10.1021/ar300197s10.1021/ar300197s ↗
5. 10.1126/science.117037710.1126/science.1170377 ↗
6. 10.1021/ja405680p10.1021/ja405680p ↗
7. 10.1126/science.124906110.1126/science.1249061 ↗
8. 10.1021/ja406806310.1021/ja4068063 ↗
9. 10.1126/science.113456910.1126/science.1134569 ↗
10. 10.1016/j.electacta.2011.10.07410.1016/j.electacta.2011.10.074 ↗
11. 10.1021/ja405504q10.1021/ja405504q ↗
12. 10.1002/chem.20120081710.1002/chem.201200817 ↗
13. 10.1021/nn405663h10.1021/nn405663h ↗
14. 10.1021/ja503315s10.1021/ja503315s ↗
15. 10.1021/ja500590n10.1021/ja500590n ↗
16. 10.1021/ja102443610.1021/ja1024436 ↗
17. 10.1002/anie.20100428710.1002/anie.201004287 ↗
18. 10.1021/ja111130t10.1021/ja111130t ↗
19. 10.1021/ja405598a10.1021/ja405598a ↗
20. 10.1021/ja406091p10.1021/ja406091p ↗
21. 10.1039/b922148d10.1039/b922148d ↗
22. 10.1149/2.006209jes10.1149/2.006209jes ↗
23. 10.1021/nl300033e10.1021/nl300033e ↗
24. 10.1038/ncomms322110.1038/ncomms3221 ↗
25. 10.1039/c2cs35173k10.1039/c2cs35173k ↗
26. 10.1007/s11244-007-9003-x10.1007/s11244-007-9003-x ↗
27. 10.1039/b823504j10.1039/b823504j ↗
28. 10.1021/jp037995310.1021/jp0379953 ↗
29. 10.1021/jp904278b10.1021/jp904278b ↗
30. 10.1021/ja806376510.1021/ja8063765 ↗
31. 10.1021/ja060167d10.1021/ja060167d ↗
32. 10.1039/c1cc11004g10.1039/c1cc11004g ↗
33. 10.1002/anie.20110125110.1002/anie.201101251 ↗
34. 10.1021/cm100155z10.1021/cm100155z ↗
35. 10.1021/cm400392e10.1021/cm400392e ↗
36. 10.1038/nmat195710.1038/nmat1957 ↗
37. 10.1126/science.121282210.1126/science.1212822 ↗
38. 10.1149/1.349041610.1149/1.3490416 ↗
39. 10.1021/jp063766f10.1021/jp063766f ↗
40. 10.1021/jp071747f10.1021/jp071747f ↗
41. 10.1021/ja017406b10.1021/ja017406b ↗
42. 10.1021/ja062892u10.1021/ja062892u ↗
43. 10.1021/ja028110o10.1021/ja028110o ↗
44. 10.1039/b711490g10.1039/b711490g ↗
45. 10.1021/jp054808n10.1021/jp054808n ↗
46. 10.1002/anie.20070409410.1002/anie.200704094 ↗
47. 10.1147/rd.221.007210.1147/rd.221.0072 ↗
48. 10.1149/1.277673210.1149/1.2776732 ↗
49. 10.1016/j.electacta.2011.03.10210.1016/j.electacta.2011.03.102 ↗
50. 10.1021/ja206361710.1021/ja2063617 ↗
51. 10.1016/j.electacta.2013.01.05210.1016/j.electacta.2013.01.052 ↗
52. 10.1016/j.jelechem.2009.10.00310.1016/j.jelechem.2009.10.003 ↗
53. 10.1021/ja900934310.1021/ja9009343 ↗
54. 10.1002/anie.20110766810.1002/anie.201107668 ↗
55. 10.1016/j.electacta.2010.09.03810.1016/j.electacta.2010.09.038 ↗
56. 10.1021/ja903305d10.1021/ja903305d ↗
57. 10.1021/ja202655j10.1021/ja202655j ↗
58. 10.1016/j.electacta.2012.08.02410.1016/j.electacta.2012.08.024 ↗
59. 10.1002/anie.20046233510.1002/anie.200462335 ↗
60. 10.1021/ja407773x10.1021/ja407773x ↗
61. 10.1038/nchem.28810.1038/nchem.288 ↗
62. 10.1021/ja907149610.1021/ja9071496 ↗
63. 10.1039/C4TA03975K10.1039/C4TA03975K ↗
64. 10.1039/C4EE01564A10.1039/C4EE01564A ↗
65. 10.1021/jp312859x10.1021/jp312859x ↗