Electrochemistry and Optical Absorbance and Luminescence of Molecule-like Au38 Nanoparticles

• Published in: Journal of the American Chemical Society 2004-05, Vol.126 (19), p.6193-6199
• Main Authors: Lee, Dongil, Donkers, Robert L, Wang, Gangli, Harper, Amanda S, Murray, Royce W
• Format: Article
• Language: English
• Subjects: Atomic and molecular clusters; Atomic and molecular physics; Exact sciences and technology; Optical properties of clusters; Physics; Studies of special atoms, molecules and their ions; clusters
• ISSN: 0002-7863; 1520-5126
• DOI: 10.1021/ja049605b

This paper describes electrochemical and spectroscopic properties of a well-characterized, synthetically accessible, 1.1 nm diam Au nanoparticle, Au38(PhC2S)24, where PhC2S is phenylethylthiolate. Properties of other Au38 nanoparticles made by exchanging the monolayer ligands with different thiolate ligands are also described. Voltammetry of the Au38 nanoparticles in CH2Cl2 reveals a 1.62 V energy gap between the first one-electron oxidation and the first reduction. Based on a charging energy correction of ca. 0.29 V, the indicated HOMO−LUMO gap energy is ca. 1.33 eV. At low energies, the optical absorbance spectrum includes peaks at 675 nm (1.84 eV) and 770 nm (1.61 eV) and an absorbance edge at ca. 1.33 eV that gives an optical HOMO−LUMO gap energy that is consistent with the electrochemical estimate. The absorbance at lowest energy is bleached upon electrochemical depletion of the HOMO level. The complete voltammetry contains two separated doublets of oxidation waves, indicating two distinct molecular orbitals, and two reduction steps. The ligand-exchanged nanoparticle Au38(PEG135S)13(PhC2S)11, where PEG135S is −SCH2CH2OCH2CH2OCH3, exhibits a broad (1.77−0.89 eV) near-IR photoluminescence band resolvable into maxima at 902 nm (1.38 eV) and 1025 nm (1.2 eV). Much of the photoluminescence occurs at energies less than the HOMO−LUMO gap energy. A working model of the energy level structure of the Au38 nanoparticle is presented.