Understanding and controlling the efficiency of Au₂₄M(SR)₁₈nanoclusters as singlet-oxygen photosensitizers

Abstract

Singlet oxygen, ¹O₂, can be generated by molecules that upon photoexcitation enable the ³O₂ → ¹O₂ transition. We used a series of atomically precise Au₂₄M(SR)₁₈ clusters, with different R groups and doping metal atoms M. Upon nanosecond photoexcitation of the cluster, ¹O₂ was efficiently generated. Detection was carried out by time-resolved electron paramagnetic resonance (TREPR) spectroscopy. The resulting TREPR transient yielded the ¹O₂ lifetime as a function of the nature of the cluster. We found that: these clusters indeed generate ¹O₂ by forming a triplet state; a more positive oxidation potential of the molecular cluster corresponds to a longer ¹O₂ lifetime; proper design of the cluster yields results analogous to those of a well-known reference photosensitizer, although more effectively. Comprehensive kinetic analysis provided important insights into the mechanism and driving-force dependence of the quenching of ¹O₂ by gold nanoclusters. Understanding on a molecular basis why these molecules may perform so well in ¹O₂ photosensitization is instrumental to controlling their performance.