Cocatalyst-free Photocatalytic Hydrogen Evolution with Simple Heteroleptic Iridium(III) Complexes
Govardhana Babu Bodedla, Daniel Nnaemaka Tritton, Xi Chen, Jianzhang Zhao, Zeling Guo, Ken Cham‐Fai Leung, Wai‐Yeung Wong, Xunjin Zhu
Abstract
A simple heteroleptic iridium(III) photosensitizer, Ir-1, containing two ligands 5-(trifluoromethyl)-2-phenylpyridine (ĈN–CF3) and bipyridine (N̂N) 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.