Light-Driven Sustainable Heck Coupling Using Copper Oxide-Pd Nanohybrid-Based Mie Resonators
Source abstract
Abstract
Photocatalysis offers a sustainable route for chemical transformations by harnessing solar light rather than relying on fossil–fuel-based heating. We have designed and synthesized nanoscale-engineered cuprous oxide and cupric oxide nanoparticles, each decorated with a thin palladium layer (Cu 2 O–Pd and CuO–Pd), to form hybrid nanostructures, creating well-defined interfaces that exploit enhanced optical properties, particularly dielectric Mie resonances and interfacial charge transfer, to drive light-assisted Heck carbon–carbon (C–C) coupling. Cu 2 O–Pd and CuO–Pd nanocatalysts achieved complete conversion to trans -stilbene within 2 h under simulated solar illumination intensity of ∼111 mW/cm 2 in a N,N-dimethylformamide (DMF)/H 2 O solvent mixture (v/v = 80:20), whereas pristine oxides were nearly inactive. Spectroscopic, microscopic, and finite-difference time-domain (FDTD) simulation analyses confirmed that nanoscale hybrid interfaces promote resonant light confinement and efficient hot-carrier generation, thereby enhancing photocatalytic activity. Notably, Cu 2 O–Pd exhibited an ∼1.56× rate enhancement under illumination compared to purely thermal conditions. These findings emphasize the distinctive nanoscale interfacial synergy at Cu 2 O–Pd interfaces and provide a rational design strategy for green cross-coupling catalysis under solar irradiation, particularly relevant to sustainable synthesis of fine chemicals and pharmaceuticals, as well as other solar-to-chemical energy conversion processes.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Copper-based nanomaterials and applications · Advanced Photocatalysis Techniques · Gold and Silver Nanoparticles Synthesis and Applications
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Department of Chemical, Biological, and Materials Engineering
University of South Florida
Department of Physics and Astronomy
West Virginia University
Department of Electrical and Computer Engineering and Petersen Institute of Nano Science and Engineering
University of Pittsburgh
Funding
National Science Foundation
References (51)
Show source-provided references
1. 10.1039/D3RA03533F10.1039/D3RA03533F ↗
2. 10.1021/acs.jpcc.8b1245310.1021/acs.jpcc.8b12453 ↗
3. 10.1016/j.rechem.2025.10217310.1016/j.rechem.2025.102173 ↗
4. 10.1038/nmat315110.1038/nmat3151 ↗
5. 10.1021/acsanm.9b0201710.1021/acsanm.9b02017 ↗
6. 10.1002/ajoc.20250052910.1002/ajoc.202500529 ↗
7. 10.1016/S1872-2067(25)64838-810.1016/S1872-2067(25)64838-8 ↗
8. 10.1016/j.inoche.2025.11564510.1016/j.inoche.2025.115645 ↗
9. 10.1002/anie.20130814510.1002/anie.201308145 ↗
10. 10.1038/s41560-019-0517-910.1038/s41560-019-0517-9 ↗
11. 10.1021/ja106910x10.1021/ja106910x ↗
12. 10.1021/ja310501y10.1021/ja310501y ↗
13. 10.1016/j.jiec.2025.09.03210.1016/j.jiec.2025.09.032 ↗
14. 10.1021/acsomega.4c0540310.1021/acsomega.4c05403 ↗
15. 10.1021/acs.chemrev.1c0019710.1021/acs.chemrev.1c00197 ↗
16. 10.1002/chin.20062808210.1002/chin.200628082 ↗
17. 10.1021/acsenergylett.7b0033310.1021/acsenergylett.7b00333 ↗
18. 10.1039/c3nr01429k10.1039/c3nr01429k ↗
19. 10.1021/ar300239310.1021/ar3002393 ↗
20. 10.1021/acsnano.5c0706310.1021/acsnano.5c07063 ↗
21. 10.1126/science.123163110.1126/science.1231631 ↗
22. 10.1021/acsanm.0c0120110.1021/acsanm.0c01201 ↗
23. 10.1021/aps.5c0000510.1021/aps.5c00005 ↗
24. 10.1021/acsmaterialslett.1c0008110.1021/acsmaterialslett.1c00081 ↗
25. 10.1016/j.mcat.2025.11554510.1016/j.mcat.2025.115545 ↗
26. 10.1021/acsami.5c0199610.1021/acsami.5c01996 ↗
27. 10.1039/C9GC01930H10.1039/C9GC01930H ↗
28. 10.1021/cs500028410.1021/cs5000284 ↗
29. 10.1021/acs.jpcc.2c0464610.1021/acs.jpcc.2c04646 ↗
30. 10.1002/adfm.20120214810.1002/adfm.201202148 ↗
31. 10.1039/9781839163128-0003810.1039/9781839163128-00038 ↗
32. 10.1002/adom.20210112810.1002/adom.202101128 ↗
33. 10.1021/acsomega.5c0783010.1021/acsomega.5c07830 ↗
34. 10.1021/acsomega.3c0276610.1021/acsomega.3c02766 ↗
35. 10.1038/ncomms958610.1038/ncomms9586 ↗
36. 10.1021/acsomega.4c0116810.1021/acsomega.4c01168 ↗
37. Copeland L. E. · 1946 · 2
38. 10.2147/IJN.S2902010.2147/IJN.S29020 ↗
39. 10.1021/acsanm.2c0073010.1021/acsanm.2c00730 ↗
40. 10.1016/j.enconman.2026.12124310.1016/j.enconman.2026.121243 ↗
41. 10.1016/j.dche.2023.10010910.1016/j.dche.2023.100109 ↗
42. 10.1021/acscatal.2c0097710.1021/acscatal.2c00977 ↗
43. 10.1063/1.349024010.1063/1.3490240 ↗
44. 10.1021/jp512500g10.1021/jp512500g ↗
45. 10.1021/acs.jpcc.3c0694110.1021/acs.jpcc.3c06941 ↗
46. 10.1117/12.300296310.1117/12.3002963 ↗
47. 10.1038/ncomms366110.1038/ncomms3661 ↗
48. 10.1021/acsomega.9b0092610.1021/acsomega.9b00926 ↗
49. 10.1016/j.fuel.2022.12734610.1016/j.fuel.2022.127346 ↗
50. 10.1103/PhysRevB.93.15515210.1103/PhysRevB.93.155152 ↗
51. 10.1038/nmat345410.1038/nmat3454 ↗