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.
more »
« less
This content will become publicly available on October 6, 2026
The nature of nanoclusters in aqueous zinc sulfate electrolytes
Transient nanoclusters in aqueous ZnSO4electrolytes are revealed with X-ray scattering and molecular dynamics simulations. These nanoclusters exhibit diverse sizes and geometries, influencing ion correlations and transport properties.
more »
« less
- Award ID(s):
- 2335833
- PAR ID:
- 10651003
- Publisher / Repository:
- RSC
- Date Published:
- Journal Name:
- EES Batteries
- Volume:
- 1
- Issue:
- 5
- ISSN:
- 3033-4071
- Page Range / eLocation ID:
- 1158 to 1172
- Format(s):
- Medium: X
- Sponsoring Org:
- National Science Foundation
More Like this
-
-
Abstract Herein, we report on the synthesis of ultrasmall Pd nanoclusters (∼2 nm) protected by L‐cysteine [HOCOCH(NH2)CH2SH] ligands (Pdn(L‐Cys)m) and supported on the surfaces of CeO2, TiO2, Fe3O4, and ZnO nanoparticles for CO catalytic oxidation. The Pdn(L‐Cys)mnanoclusters supported on the reducible metal oxides CeO2, TiO2and Fe3O4exhibit a remarkable catalytic activity towards CO oxidation, significantly higher than the reported Pd nanoparticle catalysts. The high catalytic activity of the ligand‐protected clusters Pdn(L‐Cys)mis observed on the three reducible oxides where 100 % CO conversion occurs at 93–110 °C. The high activity is attributed to the ligand‐protected Pd nanoclusters where the L‐cysteine ligands aid in achieving monodispersity of the Pd clusters by limiting the cluster size to the active sub‐2‐nm region and decreasing the tendency of the clusters for agglomeration. In the case of the ceria support, a complete removal of the L‐cysteine ligands results in connected agglomerated Pd clusters which are less reactive than the ligand‐protected clusters. However, for the TiO2and Fe3O4supports, complete removal of the ligands from the Pdn(L‐Cys)mclusters leads to a slight decrease in activity where the T100%CO conversion occurs at 99 °C and 107 °C, respectively. The high porosity of the TiO2and Fe3O4supports appears to aid in efficient encapsulation of the bare Pdnnanoclusters within the mesoporous pores of the support.more » « less
-
Abstract Au nanoclusters often demonstrate useful optical properties such as visible/near‐infrared photoluminescence, in addition to remarkable thermodynamic stability owing to their superatomic behavior. The smallest of the 8e−superatomic Au nanoclusters, Au11, has limited applications due to its lack of luminescence and relatively low stability. In this work, we investigate the introduction of a single Pt dopant to the center of a halide‐ and triphenylphosphine‐ligated Au11nanocluster, affording a cluster with a proposed molecular formula PtAu10(PPh3)7Br3. Electrochemical and spectroscopic analysis reveal an expansion of the HOMO–LUMO gap due to the Pt dopant, as well as relatively strong near‐infrared (NIR) photoluminescence which is atypical for an M11cluster (λmax= 700 nm, Φ = 1.88 %). The Pt dopant additionally boosted photostability; more than tenfold. Lastly, we demonstrate the application of the PtAu10cluster's NIR photoluminescence in the detection of the nitroaromatic compound 2,4‐dinitrotoluene, with a limit‐of‐detection of 9.52 μM (1.74 ppm). The notable ability of a single central Pt dopant to unlock photoluminescence in a non‐luminescent nanocluster highlights the advantages of heterometal doping in the tuning of both the optical and thermodynamic properties of Au nanoclusters.more » « less
An official website of the United States government
