journal article·2019-07-22

Ligand-Effect-Induced Oxygen Reduction Reaction Activity Enhancement for Pt/Zr/Pt(111) Surfaces with Tensile Strain Relieved by Stacking Faults

Daisuke Kudo, Soma Kaneko, Rikiya Myochi, Yoshihiro Chida, Naoto Todoroki, Tadao Tanabe, Toshimasa Wadayama

ACS Applied Energy Materials· Volume 2· Issue 7
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Abstract

Oxygen reduction reaction (ORR) properties are investigated for the Pt/Zr/Pt(111) surfaces prepared through arc-plasma depositions of Zr and Pt on a Pt(111) substrate. The synthesized Pt(111)-shell surfaces on Pt–Zr(111) alloy layers exhibited 3- to 5-fold higher ORR activities than the clean Pt(111): the ligand effect induced by charge transfers between Pt and Zr was considered to be the dominant activity enhancement factor, because tensile strains in the Pt-shell were relieved by the stacking faults generated in the underlaid Pt−Zr alloy layers. Furthermore, the alloy surfaces are durable against an electrochemical potential cycling. The results demonstrate that Zr should be considered for alloying elements of Pt for developments of effective ORR catalysts.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Electrocatalysts for Energy Conversion · Fuel Cells and Related Materials · Semiconductor materials and devices

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

Affiliations

Graduate School of Environmental Studies, Tohoku University, Sendai 980-8579, Japan

Graduate School of Engineering, Tohoku University, Sendai 980-8579, Japan

Funding

New Energy and Industrial Technology Development Organization

References (30)

Show source-provided references
1. 10.1016/j.jpowsour.2012.01.05910.1016/j.jpowsour.2012.01.059 ↗
2. 10.1126/science.aah613310.1126/science.aah6133 ↗
3. 10.1021/ja307951y10.1021/ja307951y ↗
4. 10.1126/science.aad889210.1126/science.aad8892 ↗
5. 10.1002/adma.20180223410.1002/adma.201802234 ↗
6. 10.1021/cs501537n10.1021/cs501537n ↗
7. 10.1039/C7CP07276G10.1039/C7CP07276G ↗
8. 10.1039/C6CS00328A10.1039/C6CS00328A ↗
9. 10.1021/acs.chemrev.7b0048810.1021/acs.chemrev.7b00488 ↗
10. 10.1021/acscatal.6b0099710.1021/acscatal.6b00997 ↗
11. 10.1016/0013-4686(94)00255-X10.1016/0013-4686(94)00255-X ↗
12. 10.1002/cctc.20110034310.1002/cctc.201100343 ↗
13. 10.1021/acs.jpclett.7b0252510.1021/acs.jpclett.7b02525 ↗
14. 10.1021/acscatal.8b0423610.1021/acscatal.8b04236 ↗
15. 10.1021/acscatal.5b0006510.1021/acscatal.5b00065 ↗
16. 10.1039/C5CP02048D10.1039/C5CP02048D ↗
17. 10.1007/s12678-019-00517-610.1007/s12678-019-00517-6 ↗
18. 10.1016/j.elecom.2010.05.04210.1016/j.elecom.2010.05.042 ↗
19. 10.1016/S1359-6454(97)00319-410.1016/S1359-6454(97)00319-4 ↗
20. 10.1021/acs.jpcc.6b1256710.1021/acs.jpcc.6b12567 ↗
21. 10.1039/C8CP01217B10.1039/C8CP01217B ↗
22. 10.1021/acscatal.6b0146610.1021/acscatal.6b01466 ↗
23. 10.1002/anie.20046233510.1002/anie.200462335 ↗
24. 10.1103/PhysRevLett.91.01610110.1103/PhysRevLett.91.016101 ↗
25. 10.1038/nchem.62310.1038/nchem.623 ↗
26. 10.1021/jz402469910.1021/jz4024699 ↗
27. 10.1103/PhysRevB.81.03340210.1103/PhysRevB.81.033402 ↗
28. 10.1039/c3cp53340a10.1039/c3cp53340a ↗
29. 10.1016/j.susc.2012.08.01610.1016/j.susc.2012.08.016 ↗
30. 10.1149/2.0571709jes10.1149/2.0571709jes ↗