Fused Porphyrin Thin Films as Heterogeneous Visible-Light Active Photocatalysts with Well-Defined Active Metal Sites for Hydrogen Generation
Source abstract
Abstract
Metalloporphyrin-based photocatalysts have attracted great interest due to their high extinction coefficient in the visible range coupled to a catalytically active central metal ion surrounded by a highly conjugated heterocyclic macrocycle. In this work, fused copper(II) porphyrin-based conjugated polymer thin films are shown to be active electrocatalysts and photocatalysts for the heterogeneous hydrogen evolution reaction (HER). The fused copper(II) porphyrin thin films notably show a significant reduction of the overpotential required for HER in comparison to the reference nonfused porphyrin thin films. More importantly, in-depth high-resolution mass spectrometry reveals how the porphyrin substituents influence the catalytic performance of the films, with phenyl substituents enabling superior photocatalytic performances over mesityl substituents, providing insights for the engineering of heterogeneous catalysts based on fused metalloporphyrins.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Electrocatalysts for Energy Conversion · Advanced Photocatalysis Techniques · Porphyrin and Phthalocyanine Chemistry
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Luxembourg Institute of Science and Technology, Materials Research and Technology Department, 41 Rue du Brill, L-4422 Belvaux, Luxembourg
Universidad Autonoma de Nuevo Leon, Facultad de Ingenieria Civil, Departmento de Ecomateriales y Energia, Av. Universidad S/N Ciudad Universitaria, San Nicolas de Los Garza, Nuevo Leon, C.P. 66455, Mexico
Funding
European Commission · Luxembourg National Research Fund
References (42)
Show source-provided references
1. 10.1021/acs.chemrev.6b0029910.1021/acs.chemrev.6b00299 ↗
2. 10.1021/acscatal.8b0177610.1021/acscatal.8b01776 ↗
3. 10.1016/j.ccr.2014.10.00110.1016/j.ccr.2014.10.001 ↗
4. 10.1021/acs.chemmater.5b0088210.1021/acs.chemmater.5b00882 ↗
5. 10.1021/ja500984k10.1021/ja500984k ↗
6. 10.1021/acscatal.0c0108510.1021/acscatal.0c01085 ↗
7. 10.1039/C7EE03115G10.1039/C7EE03115G ↗
8. 10.1039/C7TA01278K10.1039/C7TA01278K ↗
9. 10.1002/anie.20200383610.1002/anie.202003836 ↗
10. 10.1039/C8SC05247F10.1039/C8SC05247F ↗
11. 10.1002/anie.20200231110.1002/anie.202002311 ↗
12. 10.1002/aenm.20180108410.1002/aenm.201801084 ↗
13. 10.1002/aenm.20170047910.1002/aenm.201700479 ↗
14. 10.1002/adma.20150003310.1002/adma.201500033 ↗
15. 10.1021/jp101011f10.1021/jp101011f ↗
16. 10.1039/C3CS60443H10.1039/C3CS60443H ↗
17. 10.1126/science.105955210.1126/science.1059552 ↗
18. 10.1038/nchem.215910.1038/nchem.2159 ↗
19. 10.1038/nchem.260010.1038/nchem.2600 ↗
20. 10.1002/anie.20181403410.1002/anie.201814034 ↗
21. 10.1002/ejic.20200024310.1002/ejic.202000243 ↗
22. 10.1039/C9RA09711B10.1039/C9RA09711B ↗
23. 10.1002/admi.20180156410.1002/admi.201801564 ↗
24. 10.1002/chem.20190079310.1002/chem.201900793 ↗
25. 10.1002/ejoc.20190004510.1002/ejoc.201900045 ↗
26. 10.1039/a808943d10.1039/a808943d ↗
27. 10.1039/C5CP01808K10.1039/C5CP01808K ↗
28. 10.1016/0008-6223(70)90007-210.1016/0008-6223(70)90007-2 ↗
29. 10.1002/anie.19901028110.1002/anie.199010281 ↗
30. 10.1016/j.apsusc.2009.08.04810.1016/j.apsusc.2009.08.048 ↗
31. 10.1021/ja201272t10.1021/ja201272t ↗
32. 10.1021/jp809060p10.1021/jp809060p ↗
33. 10.1021/ja510442p10.1021/ja510442p ↗
34. 10.1039/C5TA02974K10.1039/C5TA02974K ↗
35. 10.1021/acs.jpclett.5b0030610.1021/acs.jpclett.5b00306 ↗
36. 10.1021/nl400258t10.1021/nl400258t ↗
37. 10.1039/C8TA10580D10.1039/C8TA10580D ↗
38. 10.1002/anie.20120247110.1002/anie.201202471 ↗
39. 10.1002/slct.20170083910.1002/slct.201700839 ↗
40. 10.3390/nano603005110.3390/nano6030051 ↗
41. 10.1039/C3NR04908F10.1039/C3NR04908F ↗
42. 10.3390/molecules17101176310.3390/molecules171011763 ↗