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Title: Cocatalyst-free photocatalytic hydrogen evolution with simple heteroleptic iridium(III) complexes
Authors: Bodedla, GB 
Tritton, DN
Chen, X
Zhao, J
Guo, Z 
Leung, KCF
Wong, WY 
Zhu, X
Issue Date: 26-Apr-2021
Source: ACS applied energy materials, 26 Apr. 2021, v. 4, no. 4, p. 3945-3951
Abstract: A simple heteroleptic iridium(III) photosensitizer, Ir-1, containing two ligands 5-(trifluoromethyl)-2-phenylpyridine (CN-CF3) and bipyridine (NN) has for the first time been studied for cocatalyst-free photocatalytic hydrogen evolution (PHE). The complex Ir-1 produces a hydrogen production rate (ηH2) of 3.2 mmol g-1 h-1, which is over 3.6-fold higher than that of the control complex Ir-2 (0.9 mmol g-1 h-1) containing bipyridine and 2-phenylpyridine ligands without CF3 groups. The higher ηH2 of Ir-1 could be ascribed to the high light-harvesting property, longer triplet electron lifetime, and more appropriate driving force for accepting electrons from the sacrificial donor, which enable efficient charge separation and transfer of electrons for hydrogen evolution. Additionally, the photostability issues of Ir-1 and Ir-2 are addressed by the selection of suitable organic solvent/water photocatalytic systems.
Keywords: Cocatalyst-free
Iridium(III) complex
Photocatalytic hydrogen evolution
Photostability and reductive quenching
Publisher: American Chemical Society
Journal: ACS applied energy materials 
EISSN: 2574-0962
DOI: 10.1021/acsaem.1c00318
Rights: © 2021 American Chemical Society
This document is the Accepted Manuscript version of a Published Work that appeared in final form in ACS Applied Energy Materials, copyright © American Chemical Society after peer review and technical editing by the publisher. To access the final edited and published work see https://doi.org/10.1021/acsaem.1c00318.
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