Mechanistic insights into the photocatalytic properties of metal nanocluster/graphene ensembles. Examining the role of visible light in the reduction of 4-nitrophenol

Metal nanoclusters (M-NCs) based on silver and gold, abbreviated as Ag-NCs and Au-NCs, respectively, were synthesized and combined with functionalized graphene, abbreviated as f-G, forming novel M-NC/f-G ensembles. The preparation of M-NCs/f-G was achieved by employing attractive electrostatic interactions developed between negatively charged M-NCs, attributed to the presence of carboxylates due to a-lipoic acid employed as a stabilizer, and positively charged f-G, attributed to the presence of ammonium units as addends. The realization of M-NC/f-G ensembles was established via titration assays as evidenced by electronic absorption and photoluminescence spectroscopy as well as scanning transmission electron microscopy (STEM) and energy-dispersive X-ray (EDX) spectroscopy analyses. Photoinduced charge-transfer phenomena were inferred within M-NCs/f-G, attributed to the suppression of MNC photoluminescence by the presence of f-G. Next, the M-NC/f-G ensembles were successfully employed as proficient catalysts for the model reduction of 4-nitrophenol to the corresponding 4-aminophenol as proof for the photoinduced hydrogen production. Particularly, the reduction kinetics decelerated by half when bare M-NCs were employed vs. the M-NC/f-G ensembles, highlighting the beneficial role of M-NCs/f-G in catalysing the process. Furthermore, Au-NCs/f-G displayed exceptionally higher catalytic activity both in the dark and under visible light illumination conditions, which is ascribed to three synergistic mechanisms, namely, (a) hydride transfer from Au-H, (b) hydride transfer from photogenerated Au-H species, and (c) hydrogen produced by the photoreduction of water. Finally, recycling and re-employing M-NCs/f-G in successive catalytic cycles without loss of activity toward the reduction of 4-nitrophenol was achieved, thereby highlighting their wider applicability.