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Synthesis of ultrasmall platinum nanoparticles and structural relaxation

[Display omitted] •A synthetic method for ultrasmall Pt nanoparticles (∼1nm) is developed.•Compared to bulk Pt, structural relaxation is observed in the Pt nanoparticles.•The Pt 4f core level energy shifts positively by +1eV compared with bulk Pt. We report the synthesis of ligand-protected, ultrasm...

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Bibliographic Details
Published in:Journal of colloid and interface science 2014-06, Vol.423 (423), p.123-128
Main Authors: Liu, Chao, Li, Gao, Kauffman, Douglas R., Pang, Guangsheng, Jin, Rongchao
Format: Article
Language:English
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Summary:[Display omitted] •A synthetic method for ultrasmall Pt nanoparticles (∼1nm) is developed.•Compared to bulk Pt, structural relaxation is observed in the Pt nanoparticles.•The Pt 4f core level energy shifts positively by +1eV compared with bulk Pt. We report the synthesis of ligand-protected, ultrasmall Pt nanoparticles of ∼1nm size via a one-phase wet chemical method. Using matrix-assisted laser desorption ionization mass spectrometry (MALDI-MS), we determined the mass of the nanoparticles to be ∼8kDa. Characterization of the Pt nanoparticles was further carried out by powder X-ray diffraction (XRD), transmission electron microscopy (TEM), thermogravimetric analysis (TGA), optical absorption spectroscopy, and X-ray photoelectron spectroscopy (XPS). Interestingly, we observed a large structural relaxation in the 8kDa nanoparticles (i.e. lattice parameter elongation by +10%) compared to bulk platinum. XPS analysis revealed a positive shift of Pt 4f core level energy by approximately +1eV compared with bulk Pt, indicating charge transfer from Pt to S atom of the thiolate ligand on the particle. Compared to bulk Pt, the 5d band of Pt nanoparticles is narrower and shifts to higher binding energy. Overall, the ∼1nm ultrasmall Pt nanoparticles exhibit quite distinct differences in electronic and structural properties compared to their larger counterparts and bulk Pt.
ISSN:0021-9797
1095-7103
DOI:10.1016/j.jcis.2014.02.022