journal article·2022-01-11

Ambient Synthesis of Pt-Reactive Metal Alloy and High-Entropy Alloy Nanocatalysts Utilizing Hydrogen Cold Plasma

Dezhen Wu, Libo Yao, Michael Ricci, Jialu Li, Rongxuan Xie, Zhenmeng Peng

Chemistry of Materials· Volume 34· Issue 1
Publisher page

Abstract

Synthesis of platinum-reactive metal alloy (Pt-RMA) and its high-entropy alloy (Pt-HEA) nanoparticles is challenging due to the huge difference in reduction potentials between Pt and reactive metal precursors and the oxyphilic nature of reactive metals. Herein, we utilize hydrogen cold plasma to synthesize a variety of Pt-RMA (Pt–Cr, Pt–Ta, Pt–V, Pt–Fe, and Pt–Al) and Pt-HEA (Pt–Cr–Ta–V–Fe–Al) nanoparticles under ambient conditions. Effectiveness of the method is attributed to the generation of hydrogen anions in hydrogen plasma, possessing extremely strong reducing ability with its −2.3 V standard reduction potential that can simultaneously reduce Pt and reactive metal precursors. The synthesized nanoparticles are characterized for confirming the alloy formation and are studied for the catalytic properties in the methanol oxidation reaction, with improved activity and durability compared to commercial Pt. This study provides an effective, universal method to synthesize Pt-RMA and Pt-HEA nanoparticles, which offers a new platform for studying this group of nanomaterials.
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Research context

OpenAlex topics: Electrocatalysts for Energy Conversion · Catalytic Processes in Materials Science · High-Temperature Coating Behaviors

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

Affiliations

Department of Chemical, Biomolecular, and Corrosion Engineering, The University of Akron, Akron, Ohio 44325, United States

Funding

National Science Foundation

References (43)

Show source-provided references
1. 10.1021/jz300563z10.1021/jz300563z ↗
2. 10.1021/ar300359w10.1021/ar300359w ↗
3. 10.1007/s12678-012-0112-310.1007/s12678-012-0112-3 ↗
4. 10.1039/b912552c10.1039/b912552c ↗
5. 10.1080/01614940.2013.79545510.1080/01614940.2013.795455 ↗
6. 10.1016/j.apcatb.2005.09.01410.1016/j.apcatb.2005.09.014 ↗
7. 10.1016/j.jechem.2017.10.00910.1016/j.jechem.2017.10.009 ↗
8. 10.1038/nature1111510.1038/nature11115 ↗
9. 10.1126/science.aaa876510.1126/science.aaa8765 ↗
10. 10.1002/cnma.20190031910.1002/cnma.201900319 ↗
11. 10.1039/c9se00082h10.1039/c9se00082h ↗
12. 10.1038/nchem.36710.1038/nchem.367 ↗
13. 10.1021/jacs.9b1081310.1021/jacs.9b10813 ↗
14. 10.1021/cm201478510.1021/cm2014785 ↗
15. 10.1039/c6ta04498k10.1039/c6ta04498k ↗
16. 10.1021/acs.inorgchem.0c0194510.1021/acs.inorgchem.0c01945 ↗
17. 10.1021/jacs.7b0136610.1021/jacs.7b01366 ↗
18. 10.1021/acscatal.6b0260310.1021/acscatal.6b02603 ↗
19. 10.1039/c1cc12448j10.1039/c1cc12448j ↗
20. 10.1016/j.jcat.2014.12.01210.1016/j.jcat.2014.12.012 ↗
21. 10.1002/cssc.20180002310.1002/cssc.201800023 ↗
22. 10.1007/s11244-013-0179-y10.1007/s11244-013-0179-y ↗
23. 10.1088/1361-6587/ab0f0910.1088/1361-6587/ab0f09 ↗
24. 10.1063/1.493146910.1063/1.4931469 ↗
25. 10.1038/s41598-017-10685-410.1038/s41598-017-10685-4 ↗
26. 10.1002/ppap.20170023410.1002/ppap.201700234 ↗
27. 10.1039/c4ta02155j10.1039/c4ta02155j ↗
28. 10.1007/s11244-017-0757-510.1007/s11244-017-0757-5 ↗
29. 10.1016/s1872-2067(15)61020-810.1016/s1872-2067(15)61020-8 ↗
30. 10.1016/j.jcou.2017.04.00910.1016/j.jcou.2017.04.009 ↗
31. 10.1126/sciadv.abg160010.1126/sciadv.abg1600 ↗
32. 10.1126/science.aan541210.1126/science.aan5412 ↗
33. 10.1016/s0257-8972(03)00290-110.1016/s0257-8972(03)00290-1 ↗
34. 10.1002/ppap.20070006610.1002/ppap.200700066 ↗
35. 10.1126/science.aad889210.1126/science.aad8892 ↗
36. 10.1116/1.57514910.1116/1.575149 ↗
37. 10.1080/02670836.1987.1178226310.1080/02670836.1987.11782263 ↗
38. 10.1038/s41529-019-0082-510.1038/s41529-019-0082-5 ↗
39. 10.1021/acsami.7b0843710.1021/acsami.7b08437 ↗
40. 10.3390/en1001004210.3390/en10010042 ↗
41. 10.1039/b703315j10.1039/b703315j ↗
42. 10.1039/c1ee01307f10.1039/c1ee01307f ↗
43. 10.1038/srep4555510.1038/srep45555 ↗