Synergistic Transition-Metal Coordination within Pyrene- and Phenanthroline-Tethered Conjugated Microporous Polymers for Boosting Hydrogen Evolution Reaction in Alkaline Media
Source abstract
Abstract
High Resolution Image Download MS PowerPoint Slide Hydrogen (H 2 ) production via electrochemical water (H 2 O) splitting relies heavily on the development of cost-effective and durable electrocatalysts to replace scarce and expensive platinum. Herein, we disclose a rationally conceived and executed synthesis of a pyrene (Py)- and phenanthroline (PhN)- tethered conjugated microporous polymer (CMP), where 1,10-phenanthroline (PhN) ligands (PyBz-PhN CMP) are incorporated through a C–Br/C–B Suzuki–Miyaura cross-coupling strategy. To enhance electrocatalytic activity, transition-metal ions (Fe 2+, Co 2+, Ni 2+, and Ru 2+ ) were coordinated with the PhN sites, affording a series of PyBz-PhN-M CMPs. Comprehensive characterization techniques, including Fourier transform infrared spectroscopy (FTIR), thermogravimetric analysis (TGA), X-ray photoelectron spectroscopy (XPS), ultraviolet photoelectron spectroscopy (UPS), and scanning electron microscopy/energy-dispersive X-ray spectroscopy (SEM-EDS), confirmed successful metal coordination, excellent structural stability, and uniform metal dispersion throughout the framework. Among these catalysts, PyBz-PhN-Ru CMP exhibited the best HER performance, achieving overpotentials of 217 mV at 10 mA cm –2 in alkaline media and 180 mV in acidic conditions, alongside a reduced charge-transfer resistance ( R ct ) of 89 Ω. Combined density functional theory (DFT) calculations and experimental results reveal that modulation of the d-band center and reduced charge-transfer barriers are key to the enhanced catalytic activity. This study demonstrates that phenanthroline-functionalized CMPs serve as versatile and tunable porous platforms for incorporating transition metals, offering a practical approach to creating efficient and low-cost HER catalysts for clean H 2 production.
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Research context
OpenAlex topics: Covalent Organic Framework Applications · Electrocatalysts for Energy Conversion · Metal-Organic Frameworks: Synthesis and Applications
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Department of Materials and Optoelectronic Science, Center for Functional Polymers and Supramolecular Materials
National Sun Yat-Sen University
Department of Chemistry, Faculty of Science
Assiut University
Department of Physics
SRM University-AP
Centre for Computational and Integrative Sciences
Department of Medicinal and Applied Chemistry
Kaohsiung Medical University
Funding
Association of Southeast Asian Nations · National Science and Technology Council
References (68)
Show source-provided references
1. 10.1016/j.renene.2024.12173310.1016/j.renene.2024.121733 ↗
2. 10.1021/acsami.3c1624410.1021/acsami.3c16244 ↗
3. 10.1021/acssuschemeng.4c0059110.1021/acssuschemeng.4c00591 ↗
4. 10.1016/j.solener.2022.09.01610.1016/j.solener.2022.09.016 ↗
5. 10.1039/D3TA07309B10.1039/D3TA07309B ↗
6. 10.1039/D5MH00735F10.1039/D5MH00735F ↗
7. 10.1002/aenm.20230025410.1002/aenm.202300254 ↗
8. 10.1039/D2SE01197B10.1039/D2SE01197B ↗
9. 10.1021/acsnano.3c0581010.1021/acsnano.3c05810 ↗
10. 10.1002/adfm.20257009810.1002/adfm.202570098 ↗
11. 10.20517/energymater.2023.11510.20517/energymater.2023.115 ↗
12. 10.1021/acs.energyfuels.2c0383310.1021/acs.energyfuels.2c03833 ↗
13. 10.1002/smtd.20180021110.1002/smtd.201800211 ↗
14. 10.1002/aenm.20190037510.1002/aenm.201900375 ↗
15. 10.1021/acscentsci.0c0108810.1021/acscentsci.0c01088 ↗
16. 10.1021/acsaem.5c0005210.1021/acsaem.5c00052 ↗
17. 10.1021/acsami.3c1862010.1021/acsami.3c18620 ↗
18. 10.1002/smll.20250325010.1002/smll.202503250 ↗
19. 10.1021/acsanm.2c0481110.1021/acsanm.2c04811 ↗
20. 10.1016/j.jpowsour.2024.23462410.1016/j.jpowsour.2024.234624 ↗
21. 10.1039/D5SC05384F10.1039/D5SC05384F ↗
22. 10.1021/acsapm.4c0236810.1021/acsapm.4c02368 ↗
23. 10.1039/D5MA00654F10.1039/D5MA00654F ↗
24. 10.1021/acsapm.5c0001210.1021/acsapm.5c00012 ↗
25. 10.1021/jacsau.4c0053710.1021/jacsau.4c00537 ↗
26. 10.1021/acsaem.4c0296810.1021/acsaem.4c02968 ↗
27. 10.1016/j.colsurfa.2025.13721410.1016/j.colsurfa.2025.137214 ↗
28. 10.1021/acsami.4c0564510.1021/acsami.4c05645 ↗
29. 10.1039/D4TA05908E10.1039/D4TA05908E ↗
30. 10.1016/j.ccr.2023.21506610.1016/j.ccr.2023.215066 ↗
31. 10.1039/D2TA09232H10.1039/D2TA09232H ↗
32. 10.1016/j.cej.2023.14473310.1016/j.cej.2023.144733 ↗
33. 10.1021/acsaem.5c0099210.1021/acsaem.5c00992 ↗
34. 10.1021/jacs.9b0122610.1021/jacs.9b01226 ↗
35. 10.1002/adfm.20240825510.1002/adfm.202408255 ↗
36. 10.1016/j.ijhydene.2025.15139010.1016/j.ijhydene.2025.151390 ↗
37. 10.1039/D5TA00244C10.1039/D5TA00244C ↗
38. 10.1039/D0PY01482F10.1039/D0PY01482F ↗
39. 10.1039/D5MA00957J10.1039/D5MA00957J ↗
40. 10.1016/j.electacta.2023.14255310.1016/j.electacta.2023.142553 ↗
41. 10.1039/C6CC06972J10.1039/C6CC06972J ↗
42. 10.1021/acs.macromol.2c0121610.1021/acs.macromol.2c01216 ↗
43. 10.1021/acs.macromol.1c0073610.1021/acs.macromol.1c00736 ↗
44. 10.1021/acspolymersau.5c0008310.1021/acspolymersau.5c00083 ↗
45. 10.1016/j.cej.2025.16589210.1016/j.cej.2025.165892 ↗
46. 10.1016/j.micromeso.2025.11362010.1016/j.micromeso.2025.113620 ↗
47. 10.1039/D3TA02847J10.1039/D3TA02847J ↗
48. 10.1039/D4CC00642A10.1039/D4CC00642A ↗
49. 10.1016/j.apcatb.2021.12010810.1016/j.apcatb.2021.120108 ↗
50. 10.1039/C5TA00993F10.1039/C5TA00993F ↗
51. 10.1021/acs.analchem.1c0455810.1021/acs.analchem.1c04558 ↗
52. 10.1021/ic700977w10.1021/ic700977w ↗
53. 10.1002/cctc.20210023010.1002/cctc.202100230 ↗
54. 10.1016/j.ijhydene.2024.11.00610.1016/j.ijhydene.2024.11.006 ↗
55. 10.1016/j.jallcom.2022.16387410.1016/j.jallcom.2022.163874 ↗
56. 10.1016/j.nanoen.2024.11054510.1016/j.nanoen.2024.110545 ↗
57. 10.1016/j.apsusc.2016.07.14610.1016/j.apsusc.2016.07.146 ↗
58. 10.1016/j.apsadv.2023.10038410.1016/j.apsadv.2023.100384 ↗
59. 10.1002/smll.20240911710.1002/smll.202409117 ↗
60. 10.1002/advs.20210591210.1002/advs.202105912 ↗
61. 10.1016/j.coelec.2022.10096110.1016/j.coelec.2022.100961 ↗
62. 10.1016/j.susmat.2021.e0025210.1016/j.susmat.2021.e00252 ↗
63. 10.1002/adma.20240315110.1002/adma.202403151 ↗
64. 10.1038/s41467-024-52520-110.1038/s41467-024-52520-1 ↗
65. 10.1038/s41467-022-34278-610.1038/s41467-022-34278-6 ↗
66. 10.1038/s41467-020-14462-210.1038/s41467-020-14462-2 ↗
67. 10.1016/S0360-0564(02)45013-410.1016/S0360-0564(02)45013-4 ↗
68. 10.1021/jacs.9b1200510.1021/jacs.9b12005 ↗