4.6 Article

Surface Structure and Silicon Nanocrystal Photoluminescence: The Role of Hypervalent Silyl Groups

Journal

JOURNAL OF PHYSICAL CHEMISTRY C
Volume 119, Issue 47, Pages 26683-26691

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.jpcc.5b08578

Keywords

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Funding

  1. MRSEC program of the National Science Foundation (NSF) [DMR-0819885, DMR-1420013]
  2. NSF under MRSEC [DMR-0819885]
  3. Michigan State University

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We report a combined experimental and theoretical study of the relationship between the surface structure of silicon nanocrystals synthesized in a nonthermal plasma reactor and their photoluminescence (PL) yields. Upon heating to 160 degrees C, a significant change in the SiH stretch region of the vibrational spectrum is observed indicating a decrease in surface SiH3 groups, which correlates with an increase in the PL yield. Effusion of SiHx and Si2H2x from the material is detected by residual gas analysis upon heating to temperatures below 200 degrees C, suggesting a weakly bound species. Analysis of electron paramagnetic resonance spectra before and after heating points to a small reduction in the density of dangling bonds upon heating but this reduction does not correlate with the increase in PL yield. Electronic structure calculations indicate that SiH3 groups may hypervalently bond to fully coordinated surface silicon atoms, resulting in a relatively weak (0.70 eV) bond that is consistent with the experimentally observed effusion at low temperature. Furthermore, nonadiabatic molecular dynamics simulations indicate that such hypervalent silyl defects provide efficient pathways for nonradiative recombination via conical intersections that are energetically accessible after near-infrared excitation.

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