journal article·2023-05-03

Enhanced Oxygen Reduction Reaction Performance by Adsorbed Water on Edge Sites

Shengwei Yu, Liyuan Chen, Na Cheng, Jiyuan Lu, Liyuan Bi, Wenhui Zhang, Aiping Chen, Haibo Jiang, Chunzhong Li

ACS Applied Materials & Interfaces· Volume 15· Issue 17
Publisher page

Abstract

Pt-based alloy nanoparticles have broad application prospects as cathode catalyst materials for proton-exchange membrane fuel cells (PEMFCs). Optimization of the oxygen adsorption energy is crucial to boost the performance of oxygen reduction catalysis. We successfully synthesized well-dispersed Pt 1.2 Ni tetrahedra and obtained the Pt 1.2 Ni/C catalyst adopting the one-pot synthetic protocol, which exhibits superb activity and good long-term stability for oxygen reduction reaction (ORR), achieving a mass activity of 1.53 A/mg Pt at 0.90 V RHE, which is 12 times higher than that of commercial Pt/C. On combining X-ray photoelectron spectroscopy and density functional theory calculations, abundant water is adsorbed stably on the Pt 1.2 Ni alloy surface. We find that the intense interaction between the adsorbed O atom and adsorbed water can weaken the adsorption of oxygen, contributing to the ORR performance.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Electrocatalysts for Energy Conversion · Fuel Cells and Related Materials · Electrochemical Analysis and Applications

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

Shanghai Engineering Research Center of Hierarchical Nanomaterials, Key Laboratory for Ultrafine Materials of Ministry of Education, School of Materials Science and Engineering, East China University of Science & Technology, Shanghai 200237, China

Funding

Central University Basic Research Fund of China · Shanghai Municipal Education Commission · Science and Technology Commission of Shanghai Municipality · National Natural Science Foundation of China · Social Development Program of Shanghai

References (37)

Show source-provided references
1. 10.1021/acs.nanolett.0c0281210.1021/acs.nanolett.0c02812 ↗
2. 10.1002/aenm.20160023610.1002/aenm.201600236 ↗
3. 10.1021/acs.chemrev.5b0046210.1021/acs.chemrev.5b00462 ↗
4. 10.1021/cr500519c10.1021/cr500519c ↗
5. 10.1021/acscatal.9b0315510.1021/acscatal.9b03155 ↗
6. 10.1126/science.aaa876510.1126/science.aaa8765 ↗
7. 10.1002/advs.20190127910.1002/advs.201901279 ↗
8. 10.1021/jacs.7b0103610.1021/jacs.7b01036 ↗
9. 10.1002/anie.20210101910.1002/anie.202101019 ↗
10. 10.1021/acsnano.9b0196110.1021/acsnano.9b01961 ↗
11. 10.1021/acscatal.8b0450510.1021/acscatal.8b04505 ↗
12. 10.1021/acs.chemrev.7b0048810.1021/acs.chemrev.7b00488 ↗
13. 10.1021/jp047349j10.1021/jp047349j ↗
14. 10.1021/cs300227s10.1021/cs300227s ↗
15. 10.1126/science.aab080110.1126/science.aab0801 ↗
16. 10.1126/science.124906110.1126/science.1249061 ↗
17. 10.1021/jp904278b10.1021/jp904278b ↗
18. 10.1002/anie.20140649710.1002/anie.201406497 ↗
19. 10.1021/acs.nanolett.9b0086710.1021/acs.nanolett.9b00867 ↗
20. 10.1021/ja303950v10.1021/ja303950v ↗
21. 10.1021/acsami.0c0586810.1021/acsami.0c05868 ↗
22. 10.1073/pnas.210402611810.1073/pnas.2104026118 ↗
23. 10.1021/jacs.6b0035910.1021/jacs.6b00359 ↗
24. 10.1039/C6CY02344D10.1039/C6CY02344D ↗
25. 10.1021/jz100241j10.1021/jz100241j ↗
26. 10.1016/j.apcatb.2019.11808010.1016/j.apcatb.2019.118080 ↗
27. 10.1021/acscatal.9b0320610.1021/acscatal.9b03206 ↗
28. 10.1021/acs.jpcc.9b0445710.1021/acs.jpcc.9b04457 ↗
29. 10.1039/D1CY01258D10.1039/D1CY01258D ↗
30. 10.1021/acsami.8b2166110.1021/acsami.8b21661 ↗
31. 10.1016/S0167-5729(01)00020-610.1016/S0167-5729(01)00020-6 ↗
32. 10.1021/acscatal.0c0313710.1021/acscatal.0c03137 ↗
33. 10.1002/anie.20050438610.1002/anie.200504386 ↗
34. 10.1002/anie.20210030710.1002/anie.202100307 ↗
35. 10.1016/j.nanoen.2019.10389010.1016/j.nanoen.2019.103890 ↗
36. 10.1149/1.300800510.1149/1.3008005 ↗
37. 10.1038/s41586-021-04068-z10.1038/s41586-021-04068-z ↗