Plasmon-Enhanced Hydrogenation of 1-Dodecene and Toluene Using Ruthenium-Coated Gold Nanoparticles
Source abstract
Abstract
While a key reaction for oil upgrade, the hydrogenation of arenes substrates remains a challenging one, requiring the use of transition-metal catalysts and harsher reaction conditions than classic hydrogenation processes. We designed a photocatalyst by deposition of Ru clusters onto plasmonic Au nanoparticles to accelerate this reaction, as well as the hydrogenation of alkenes. Light irradiation triggered an order of magnitude increase in the reaction rate for the hydrogenation of 1-dodecene and toluene at room temperature and under atmospheric to mild H2 pressures. The localized surface plasmon resonance featured by the supporting Au nanoparticles explains this interesting reactivity and was fully characterized by electron energy loss spectroscopy (EELS). A potential mechanism is proposed to explain this light-induced reactivity enhancement.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Electrocatalysts for Energy Conversion · Catalytic Processes in Materials Science · Catalysis and Hydrodesulfurization Studies
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Centre in Green Chemistry and Catalysis, Department of Chemistry, McGill University, Montréal, Québec H3A 0B8, Canada
Department of Mining and Materials Engineering, McGill University, Montréal, Québec H3A 0C5, Canada
Funding
Canada Foundation for Innovation · Fonds de Recherche du Québec - Nature et Technologies · Natural Sciences and Engineering Research Council of Canada
References (43)
Show source-provided references
1. 10.1021/es506172610.1021/es5061726 ↗
2. 10.1016/j.atmosenv.2007.12.01010.1016/j.atmosenv.2007.12.010 ↗
3. 10.15255/CABEQ.2016.95910.15255/CABEQ.2016.959 ↗
4. 10.1080/0161494940801392110.1080/01614949408013921 ↗
5. 10.1016/S0926-860X(03)00314-410.1016/S0926-860X(03)00314-4 ↗
6. 10.1039/a807447j10.1039/a807447j ↗
7. 10.1016/j.apsusc.2019.05.02910.1016/j.apsusc.2019.05.029 ↗
8. 10.1002/cctc.20170164410.1002/cctc.201701644 ↗
9. 10.1016/S0166-9834(00)82608-110.1016/S0166-9834(00)82608-1 ↗
10. 10.1021/ja101602d10.1021/ja101602d ↗
11. Livingstone S. E. · 1973 · 25
12. Hagelüken C. · Metall · 2006 · 60 · 31
13. 10.1002/chem.20030576510.1002/chem.200305765 ↗
14. 10.1002/adsc.20039001510.1002/adsc.200390015 ↗
15. 10.1039/C5RA08675B10.1039/C5RA08675B ↗
16. 10.1039/C8TA12353E10.1039/C8TA12353E ↗
17. 10.1021/acs.chemrev.9b0018710.1021/acs.chemrev.9b00187 ↗
18. 10.1016/j.cocis.2019.01.01410.1016/j.cocis.2019.01.014 ↗
19. 10.1002/adma.20200008610.1002/adma.202000086 ↗
20. 10.1016/j.matt.2020.03.01910.1016/j.matt.2020.03.019 ↗
21. 10.1021/acsami.0c1519210.1021/acsami.0c15192 ↗
22. 10.1039/C7EE02951A10.1039/C7EE02951A ↗
23. 10.1016/j.apcatb.2019.11782310.1016/j.apcatb.2019.117823 ↗
24. 10.1002/anie.20160174010.1002/anie.201601740 ↗
25. 10.1002/chem.20170574910.1002/chem.201705749 ↗
26. 10.1038/nmat345410.1038/nmat3454 ↗
27. 10.1021/nl303940z10.1021/nl303940z ↗
28. 10.1021/acscatal.7b0212810.1021/acscatal.7b02128 ↗
29. 10.1021/acssuschemeng.5b0104810.1021/acssuschemeng.5b01048 ↗
30. 10.1023/A:101917733081010.1023/A:1019177330810 ↗
31. 10.1073/pnas.160976911310.1073/pnas.1609769113 ↗
32. 10.1021/acsnano.8b0035210.1021/acsnano.8b00352 ↗
33. 10.1039/C5TA00777A10.1039/C5TA00777A ↗
34. 10.1039/C7RA07264C10.1039/C7RA07264C ↗
35. 10.1021/acs.nanolett.8b0349910.1021/acs.nanolett.8b03499 ↗
36. 10.1039/C4CE02560A10.1039/C4CE02560A ↗
37. 10.1039/b402823f10.1039/b402823f ↗
38. 10.1021/la010432310.1021/la0104323 ↗
39. 10.1039/b604038c10.1039/b604038c ↗
40. 10.1038/s41377-020-00345-010.1038/s41377-020-00345-0 ↗
41. Carter C. B. · 201610.1007/978-3-319-26651-0 ↗
42. 10.1017/S143192761600110010.1017/S1431927616001100 ↗
43. 10.1016/j.ultramic.2018.12.01510.1016/j.ultramic.2018.12.015 ↗