Effect of anchoring groups on the photocatalytic performance of iridium(III) complexes in hydrogen production and their toxicological analysis

Abstract

Three iridium(III) complexes (Ir1–Ir3) with different anchoring moieties, namely, 4,4'-dinitro-2,2'-bipyridine, tetraethyl [2,2ʹ‐bipyridine]‑4,4ʹ‐diylbis(phosphonate), and diethyl [2,2ʹ‐bipyridine]‑4,4ʹ‐dicarboxylate were designed, synthesised, and used as photosensitisers for water-splitting hydrogen generation. The effects of these anchoring moieties on the photophysical and electrochemical characteristics of the Ir(III) complexes were investigated via density functional theory (DFT) simulations and experimental methods. The hydrogen production efficiency of the Ir1@Pt-TiO2 system was as high as 4020.27 mol·μg−1·h−1. Among the three anchoring moieties, tetraethyl [2,2ʹ‑bipyridine]‑4,4ʹ‑diylbis(phosphonate) improved the performance of the complexes to a greater extent. In addition, toxicological investigation revealed that the toxicity of the Ir(III) complexes to luminous bacteria did not differ significantly from that of TiO2. This implies that the Ir(III) complexes synthesised in this study do not pose a significant threat to marine environments, similar to TiO2. This finding has potential implications in the development of highly efficient Ir(III) photosensitisers for the water-splitting process for hydrogen production.