Abstract
Quantum confinement in nanoscale Si structures is widely believed to be responsible for the visible luminescence observed from anodically etched porous silicon (por-Si), but little is known about the actual size or shape of these structures. Extended x-ray absorption fine structure data from a wide variety of por-Si samples show significantly reduced average Si coordination numbers due to the sizable contribution of surface-coordinated H. (The H/Si ratios, as large as 1.2, were independently confirmed by ir-absorption and α-recoil measurements.) The Si coordinations imply very large surface/volume ratios, enabling the average Si structures to be identified as crystalline particles (not wires) whose dimensions are typically <15 Å. Comparison of the size-dependent peak luminescence energies with those of oxidized Si nanocrystals, whose shapes are known, shows remarkable agreement. Furthermore, near-edge x-ray absorption fine structure measurements of the nanocrystals shows the outer oxide and interfacial suboxide layers to be constant over a wide range of nanocrystal sizes. The combination of these results effectively rules out surface species as being responsible for the observed visible luminescence in por-Si, and strongly supports quantum confinement as the dominant mechanism occurring in Si particles which are substantially smaller than previously reported or proposed.
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For a Si cube of side L, NSi = 8L 3/a 0 3; for a sphere of diameter L, NSi sph = (π/6)NSi cube.
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Schuppler, S., Friedman, S.L., Marcus, M.A. et al. X-Ray Absorption Spectroscopy from H-Passivated Porous Si and Oxidized Si Nanocrystals. MRS Online Proceedings Library 375, 113–120 (1994). https://doi.org/10.1557/PROC-375-113
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DOI: https://doi.org/10.1557/PROC-375-113