TY - JOUR
T1 - Surface brightens up Si quantum dots: direct bandgap-like size-tunable emission
AU - Dohnalova, K.
AU - Poddubny, A.N.
AU - Prokofiev, A.A.
AU - Dam-de Boer, W.
AU - Umesh, C.P.
AU - Paulusse, Jos Marie Johannes
AU - Zuilhof, H.
AU - Gregorkiewicz, T.
PY - 2013
Y1 - 2013
N2 - Colloidal semiconductor quantum dots (QDs) constitute a perfect material for ink-jet printable large area displays, photovoltaics, light-emitting diode, bio-imaging luminescent markers and many other applications. For this purpose, efficient light emission/absorption and spectral tunability are necessary conditions. These are currently fulfilled by the direct bandgap materials. Si-QDs could offer the solution to major hurdles posed by these materials, namely, toxicity (e.g., Cd-, Pb- or As-based QDs), scarcity (e.g., QD with In, Se, Te) and/or instability. Here we show that by combining quantum confinement with dedicated surface engineering, the biggest drawback of Si—the indirect bandgap nature—can be overcome, and a ‘direct bandgap’ variety of Si-QDs is created. We demonstrate this transformation on chemically synthesized Si-QDs using state-of-the-art optical spectroscopy and theoretical modelling. The carbon surface termination gives rise to drastic modification in electron and hole wavefunctions and radiative transitions between the lowest excited states of electron and hole attain ‘direct bandgap-like’ (phonon-less) character. This results in efficient fast emission, tunable within the visible spectral range by QD size. These findings are fully justified within a tight-binding theoretical model. When the C surface termination is replaced by oxygen, the emission is converted into the well-known red luminescence, with microsecond decay and limited spectral tunability. In that way, the ‘direct bandgap’ Si-QDs convert into the ‘traditional’ indirect bandgap form, thoroughly investigated in the past.
Keywords:
direct bandgap; optical spectroscopy; optoelectronics; organic capping; silicon quantum dots; tight binding model
AB - Colloidal semiconductor quantum dots (QDs) constitute a perfect material for ink-jet printable large area displays, photovoltaics, light-emitting diode, bio-imaging luminescent markers and many other applications. For this purpose, efficient light emission/absorption and spectral tunability are necessary conditions. These are currently fulfilled by the direct bandgap materials. Si-QDs could offer the solution to major hurdles posed by these materials, namely, toxicity (e.g., Cd-, Pb- or As-based QDs), scarcity (e.g., QD with In, Se, Te) and/or instability. Here we show that by combining quantum confinement with dedicated surface engineering, the biggest drawback of Si—the indirect bandgap nature—can be overcome, and a ‘direct bandgap’ variety of Si-QDs is created. We demonstrate this transformation on chemically synthesized Si-QDs using state-of-the-art optical spectroscopy and theoretical modelling. The carbon surface termination gives rise to drastic modification in electron and hole wavefunctions and radiative transitions between the lowest excited states of electron and hole attain ‘direct bandgap-like’ (phonon-less) character. This results in efficient fast emission, tunable within the visible spectral range by QD size. These findings are fully justified within a tight-binding theoretical model. When the C surface termination is replaced by oxygen, the emission is converted into the well-known red luminescence, with microsecond decay and limited spectral tunability. In that way, the ‘direct bandgap’ Si-QDs convert into the ‘traditional’ indirect bandgap form, thoroughly investigated in the past.
Keywords:
direct bandgap; optical spectroscopy; optoelectronics; organic capping; silicon quantum dots; tight binding model
KW - IR-89895
KW - METIS-293901
U2 - 10.1038/lsa.2013.3
DO - 10.1038/lsa.2013.3
M3 - Article
VL - 2
SP - e47-
JO - Light : science & applications
JF - Light : science & applications
SN - 2095-5545
IS - e47
M1 - e47
ER -