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The excited state behavior of Au₁₈(SR)₁₄nanoclusters can be controlled by tailoring the surface ligands; specifically, the aromatic ligands’ networking can promote the intersystem crossing in Au₁₈(SR)₁₄compared to the case of non-aromatic ligands. 

Abstract Photoluminescence of ultrasmall, atomically precise gold nanoclusters constitutes an area of significant interest in recent years for both fundamental research and biological applications. However, the exploration of near-infrared photoluminescence of gold nanoclusters is still in its infancy due to the limitations of synthetic methods and characterization techniques. Herein, the photoluminescence properties of an Au₃₈(PET)₂₆(PET = 2-phenylethanethiolate) nanocluster are investigated in detail. The Au₃₈(PET)₂₆exhibits an emission peak at 865 nm, which is revealed to be a mix of fluorescence, thermally activated delayed fluorescence, and phosphorescence via the combined analyses of time-resolved and temperature-dependent photoluminescence measurements. The quantum yield of Au₃₈(PET)₂₆is determined to be 1.8% at room temperature under ambient conditions, which increases to above 90% by suppressing the non-radiative relaxation pathway at a cryogenic temperature (80 K). Overall, the results of this work discover the coexistence of three radiative processes in thiolate-protected Au nanoclusters and will pave the way for understanding the intriguing photoluminescence properties of gold nanoclusters in future studies. 

The metallic bond is arguably the most intriguing one among the three types of chemical bonds, and the resultant plasmon excitation ( e.g. in gold nanoparticles) has garnered wide interest. Recent progress in nanochemistry has led to success in obtaining atomically precise nanoclusters (NCs) of hundreds of atoms per core. In this work, thiolate-protected Au 279 (SR) 84 and Au 333 (SR) 79 NCs, both in the nascent metallic state are investigated by cryogenic optical spectroscopy down to 2.5 K. At room temperature, both NCs exhibit distinct plasmon resonances, albeit the NCs possess a gap (estimated 0.02–0.03 eV, comparable to thermal energy). Interestingly, we observe no effect on plasmons with the transition from the metallic state at r.t. to the insulating state at cryogenic temperatures (down to 2.5 K), indicating a nonthermal origin for electron-gas formation. The electronic screening-induced birth of metallic state/bonding is discussed. The obtained insights offer deeper understanding of the nascent metallic state and covalent-to-metallic bonding evolution, as well as plasmon birth from concerted excitonic transitions. 

Abstract This work investigates the critical factors impacting electrochemical CO₂reduction reaction (CO₂RR) using atomically precise Au nanoclusters (NCs) as electrocatalysts. First, the influence of size on CO₂RR is studied by precisely controlling NC size in the 1–2.5 nm regime. We find that the electrocatalytic CO partial current density increases for smaller NCs, but the CO Faradaic efficiency (FE) is not directly associated with the NC size. This indicates that the surface‐to‐volume ratio, i.e. the population of active sites, is the dominant factor for determining the catalytic activity, but the selectivity is not directly impacted by size. Second, we compare the CO₂RR performance of Au₃₈isomers (Au₃₈Q and Au₃₈T) to reveal that structural rearrangement of identical size NCs can lead to significant changes in both CO₂RR activity and selectivity. Au₃₈Q shows higher activity and selectivity towards CO than Au₃₈T, and density functional theory (DFT) calculations reveal that the average formation energy of the key *COOH intermediate on the proposed active sites is significantly lower on Au₃₈Q than Au₃₈T. These results demonstrate how the structural isomerism can impact stabilization of reaction intermediates as well as the overall CO₂RR performance of identical size Au NCs. Overall, this work provides important structure–property relationships for tailoring the NCs for CO₂RR.