ABSTRACT
Chiral gold nanoclusters offer significant potential for exploring chirality at a fundamental level and for exploiting their applications in sensing and catalysis. However, their widespread use is impeded by low yields in synthesis, tedious separation procedures of their enantiomeric forms, and limited thermal stability. In this study, we investigated the direct synthesis of enantiopure chiral nanoclusters using the chiral ligand 2-MeBuSH in the fabrication of Au25, Au38, and Au144 nanoclusters. Notably, this approach leads to the unexpected formation of intrinsically chiral clusters with high yields for chiral Au38 and Au144 nanoclusters. Experimental evaluation of chiral activity by circular dichroism (CD) spectroscopy corroborates previous theoretical calculations, highlighting the stronger CD signal exhibited by Au144 compared to Au38 or Au25. Furthermore, the formation of a single enantiomeric form is experimentally confirmed by comparing it with intrinsically chiral Au38(2-PET)24 (2-PET: 2-phenylethanethiol) and is supported theoretically for both Au38 and Au144. Moreover, the prepared chiral clusters show stability against diastereoisomerization, up to temperatures of 80 °C. Thus, our findings not only demonstrate the selective preparation of enantiopure, intrinsically chiral, and highly stable thiolate-protected Au nanoclusters through careful ligand design but also support the predicted "super" chirality in the Au144 cluster, encompassing hierarchical chirality in ligands, staple configuration, and core structure.
ABSTRACT
The reactivity of supported monolayer protected Au nanoclusters is directly affected by their structural dynamics under pretreatment and reaction conditions. The effect of different types of ligands of Au clusters supported on CeO2 on their core structure evolution, under oxidative pretreatment and CO oxidation reaction, was investigated. X-ray absorption and X-ray photoelectron spectroscopy studies revealed that the clusters evolve to a similar core structure above 250 °C in all the cases, indicating the active role of the ligand-support interaction in the reaction.
ABSTRACT
Monolayer protected Au nanocluster catalysts are known to undergo structural changes during catalytic reactions, including dissociation and migration of ligands onto the support, which strongly affects their activity and stability. To better understand how the nature of ligands influences the catalytic activity of such catalysts, three types of ceria supported Au nanoclusters with different kinds of ligands (thiolates, phosphines and a mixture thereof) have been studied, employing CO oxidation as model reaction. The thiolate-protected Au25/CeO2 showed significantly higher CO conversion after activation at 250 °C than the cluster catalysts possessing phosphine ligands. Temperature programmed oxidation and inâ situ infrared spectroscopy revealed that while the phosphine ligands seemed to decompose and free Au surface was exposed, temperatures higher than 250 °C are required to efficiently remove them from the whole catalyst system. Moreover, the presence of residues on the support seemed to have much greater influence on the reactivity than the gold particle size.
ABSTRACT
Replacement of protecting ligands of gold nanoclusters by ligand exchange has become an established post-synthetic tool for selectively modifying the nanoclusters' properties. Several Au nanoclusters are known to additionally undergo size transformations upon ligand exchange, enabling access to cluster structures that are difficult to obtain by direct synthesis. This work reports on the selective size transformation of Au15(SG)13 (SG: glutathione) nanoclusters to Au16(2-PET)14 (2-PET: 2-phenylethanethiol) nanoclusters through a two-phase ligand exchange process at room temperature. Among several parameters evaluated, the addition of a large excess of exchange thiol (2-PET) to the organic phase was identified as the key factor for the structure conversion. After exchange, the nature of the clusters was determined by UV-vis, electrospray ionization-time of flight mass spectrometry, attenuated total reflection-Fourier transform infrared, and extended x-ray absorption fine-structure spectroscopy. The obtained Au16(2-PET)14 clusters proved to be exceptionally stable in solution, showing only slightly diminished UV-vis absorption features after 3 days, even when exposed to an excess of thiol ligands.
ABSTRACT
Doping gold nanoclusters with palladium has been reported to increase their catalytic activity and stability. PdAu24 nanoclusters, with the Pd dopant atom located at the center of the Au cluster core, were supported on titania and applied in catalytic CO oxidation, showing significantly higher activity than supported monometallic Au25 nanoclusters. After pretreatment, operando DRIFTS spectroscopy detected CO adsorbed on Pd during CO oxidation, indicating migration of the Pd dopant atom from the Au cluster core to the cluster surface. Increasing the number of Pd dopant atoms in the Au structure led to incorporation of Pd mostly in the S-(M-S) n protecting staples, as evidenced by in situ XAFS. A combination of oxidative and reductive thermal pretreatment resulted in the formation of isolated Pd surface sites within the Au surface. The combined analysis of in situ XAFS, operando DRIFTS, and ex situ XPS thus revealed the structural evolution of bimetallic PdAu nanoclusters, yielding a Pd single-site catalyst of 2.7 nm average particle size with improved CO oxidation activity.
ABSTRACT
Atomically precise thiolate protected Au nanoclusters Au38(SC2H4Ph)24 on CeO2 were used for in-situ (operando) extended X-ray absorption fine structure/diffuse reflectance infrared fourier transform spectroscopy and ex situ scanning transmission electron microscopy-high-angle annular dark-field imaging/X-ray photoelectron spectroscopy studies monitoring cluster structure changes induced by activation (ligand removal) and CO oxidation. Oxidative pretreatment at 150 °C "collapsed" the clusters' ligand shell, oxidizing the hydrocarbon backbone, but the S remaining on Au acted as poison. Oxidation at 250 °C produced bare Au surfaces by removing S which migrated to the support (forming Au+-S), leading to highest activity. During reaction, structural changes occurred via CO-induced Au and O-induced S migration to the support. The results reveal the dynamics of nanocluster catalysts and the underlying cluster chemistry.
ABSTRACT
The properties of gold nanoclusters, apart from being size-dependent, are strongly related to the nature of the protecting ligand. Ligand exchange on Au nanoclusters has been proven to be a powerful tool for tuning their properties, but has so far been limited to dissolved clusters in solution. By supporting the clusters previously functionalized in solution, it is uncertain that the functionality is still accessible once the cluster is on the surface. This may be overcome by introducing the desired functionality by ligand exchange after the cluster deposition on the support material. We herein report the first successful ligand exchange on supported (immobilized) Au11 nanoclusters. Dropcast films of Au11(PPh3)7Br3 on planar oxide surfaces were shown to react with thiol ligands, resulting in clusters with a mixed ligand shell, with both phosphines and thiolates being present. Laser ablation inductively coupled plasma mass spectrometry and infrared spectroscopy confirmed that the exchange just takes place on the cluster dropcast. Contrary to systems in solution, the size of the clusters did not increase during ligand exchange. Different structures/compounds were formed depending on the nature of the incoming ligand. The feasibility to extend ligand engineering to supported nanoclusters is proven and it may allow controlled nanocluster functionalization.
ABSTRACT
Thiolate protected metal clusters are valuable precursors for the design of tailored nanosized catalysts. Their performance can be tuned precisely at atomic level, e. g. by the configuration/type of ligands or by partial/complete removal of the ligand shell through controlled pre-treatment steps. However, the interaction between the ligand shell and the oxide support, as well as ligand removal by oxidative pre-treatment, are still poorly understood. Typically, it was assumed that the thiolate ligands are simply converted into SO2, CO2 and H2O. Herein, we report the first detailed observation of sulfur ligand migration from Au to the oxide support upon deposition and oxidative pre-treatment, employing mainly S K-edge XANES. Consequently, thiolate ligand migration not only produces clean Au cluster surfaces but also the surrounding oxide support is modified by sulfur-containing species, with pronounced effects on catalytic properties.