5 years ago

Oxidant-Activated Reactions of Nucleophiles with Silicon Nanocrystals

Oxidant-Activated Reactions of Nucleophiles with Silicon Nanocrystals
Jonathan R. Thompson, Nathan S. Lewis, Mita Dasog
The oxidant-activated reactivity of Si toward nucleophiles was evaluated for Si nanocrystals (Si-NCs) of differing diameters, d. In the presence of ferrocenium as a one-electron, outer-sphere oxidant, d ≥ 8 nm Si-NCs readily reacted with nucleophiles, including methanol, butanol, butylamine, butanoic acid, butylthiol, and diethylphosphine. However, d < 8 nm Si-NCs did not undergo such reactions, and stronger oxidants such as acetylferrocenium or 1,1′-diacetylferrocenium were required. Butylamine-, butylthiol-, and butanol-functionalized d ≥ 8 nm Si-NCs were partially oxidized and exhibited photoluminescence originating from defect states. In contrast, butanoic acid-functionalized Si-NCs were minimally oxidized and displayed core emission resulting from the excitation and relaxation of electrons across the Si-NC bandgap. Diethylphosphine-functionalized Si-NCs were stable only under inert conditions and showed core emission, with the Si–P bonds being highly susceptible to oxidation and rapidly decomposing upon exposure to ambient conditions. The general reactivity is consistent with the redox potential of the one-electron oxidant and the valence band edge position of the Si-NCs. The trends in reactivity thus provide an example of differential chemical reactions of nanoparticles relative to bulk materials, reflecting the differences in electronic structure and the continuum of electronic properties between variously sized Si nanoparticles and bulk Si samples.

Publisher URL: http://dx.doi.org/10.1021/acs.chemmater.7b02572

DOI: 10.1021/acs.chemmater.7b02572

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