Abstract
Electrocatalytic hydrogen production via transition metal complexes offers a promising approach for chemical energy storage. Optimal platforms to effectively control the proton and electron transfer steps en route to H-2 evolution still need to be established, and redox-active ligands could play an important role in this context. In this study, we explore the role of the redox-active Mabiq (Mabiq = 2-4:6-8-bis(3,3,4,4-tetramethlyldihydropyrrolo)-10-15-(2,2-biquinazolino)-[15]- 1,3,5,8,10,14-hexaene1,3,7,9,11,14-N-6) ligand in the hydrogen evolution reaction (HER). Using spectro-electrochemical studies in conjunction with quantum chemical calculations, we identified two precatalytic intermediates formed upon the addition of two electrons and one proton to [CoII(Mabiq)(THF)](PF6) (Co-Mbq). We further examined the acid strength effect on the generation of the intermediates. The generation of the first intermediate, Co-Mbq-H-1, involves proton addition to the bridging imine-nitrogen atom of the ligand and requires strong proton activity. The second intermediate, Co-Mbq-H-2, acquires a proton at the diketiminate carbon for which a weaker proton activity is sufficient. We propose two decoupled H-2 evolution pathways based on these two intermediates, which operate at different overpotentials. Our results show how the various protonation sites of the redox-active Mabiq ligand affect the energies and activities of HER intermediates.
Item Type: | Journal article |
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Faculties: | Chemistry and Pharmacy > Department of Chemistry |
Subjects: | 500 Science > 540 Chemistry |
ISSN: | 0020-1669 |
Language: | English |
Item ID: | 102600 |
Date Deposited: | 05. Jun 2023, 15:40 |
Last Modified: | 05. Jun 2023, 15:40 |