Deciphering the photophysical kinetics, electronic configurations and structural conformations of iridium–cobalt hydrogen evolution photocatalysts
- Instituto de Ciencia de Materiales de Madrid, Madrid (Spain)
- Institute of Condensed Matter and Nanoscience, Louvain-la-Neuve (Belgium)
- Argonne National Laboratory (ANL), Lemont, IL (United States)
- Marquette University, Milwaukee, WI (United States)
Picosecond optical and X-ray absorption spectroscopies with time-dependent density functional theory revealed the reaction pathways, electronic and structural conformations of Ir–Co hydrogen evolution photocatalysts. The dyad bearing 2-phenylpyridine ancillary ligands produced more photoreduced Co(II) than its 2-phenylisoquinoline analogue. These findings are important for designs of earth-abundant photosensitizers for photocatalytic applications.
- Research Organization:
- Argonne National Laboratory (ANL), Lemont, IL (United States)
- Sponsoring Organization:
- USDOE Office of Science (SC), Basic Energy Sciences (BES)
- Grant/Contract Number:
- AC02-06CH11357
- OSTI ID:
- 1970702
- Journal Information:
- ChemComm, Journal Name: ChemComm Journal Issue: 58 Vol. 58; ISSN 1359-7345
- Publisher:
- Royal Society of ChemistryCopyright Statement
- Country of Publication:
- United States
- Language:
- English
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