TY - JOUR
T1 - Structural investigations of silicon nanostructures grown by self-organized island formation for photovoltaic applications
AU - Roczen, Maurizio
AU - Schade, Martin
AU - Malguth, Enno
AU - Callsen, Gordon
AU - Barthel, Thomas
AU - Gref, Orman
AU - Töfflinger, Jan A.
AU - Schöpke, Andreas
AU - Schmidt, Manfred
AU - Leipner, Hartmut S.
AU - Ruske, Florian
AU - Phillips, Matthew R.
AU - Hoffmann, Axel
AU - Korte, Lars
AU - Rech, Bernd
PY - 2012/9
Y1 - 2012/9
N2 - The self-organized growth of crystalline silicon nanodots and their structural characteristics are investigated. For the nanodot synthesis, thin amorphous silicon (a-Si) layers with different thicknesses have been deposited onto the ultrathin (2 nm) oxidized (111) surface of Si wafers by electron beam evaporation under ultrahigh vacuum conditions. The solid phase crystallization of the initial layer is induced by a subsequent in situ annealing step at 700°C, which leads to the dewetting of the initial a-Si layer. This process results in the self-organized formation of highly crystalline Si nanodot islands. Scanning electron microscopy confirms that size, shape, and planar distribution of the nanodots depend on the thickness of the initial a-Si layer. Cross-sectional investigations reveal a single-crystalline structure of the nanodots. This characteristic is observed as long as the thickness of the initial a-Si layer remains under a certain threshold triggering coalescence. The underlying ultra-thin oxide is not structurally affected by the dewetting process. Furthermore, a method for the fabrication of close-packed stacks of nanodots is presented, in which each nanodot is covered by a 2 nm thick SiO 2 shell. The chemical composition of these ensembles exhibits an abrupt Si/SiO 2 interface with a low amount of suboxides. A minority charge carrier lifetime of 18 μs inside of the nanodots is determined.
AB - The self-organized growth of crystalline silicon nanodots and their structural characteristics are investigated. For the nanodot synthesis, thin amorphous silicon (a-Si) layers with different thicknesses have been deposited onto the ultrathin (2 nm) oxidized (111) surface of Si wafers by electron beam evaporation under ultrahigh vacuum conditions. The solid phase crystallization of the initial layer is induced by a subsequent in situ annealing step at 700°C, which leads to the dewetting of the initial a-Si layer. This process results in the self-organized formation of highly crystalline Si nanodot islands. Scanning electron microscopy confirms that size, shape, and planar distribution of the nanodots depend on the thickness of the initial a-Si layer. Cross-sectional investigations reveal a single-crystalline structure of the nanodots. This characteristic is observed as long as the thickness of the initial a-Si layer remains under a certain threshold triggering coalescence. The underlying ultra-thin oxide is not structurally affected by the dewetting process. Furthermore, a method for the fabrication of close-packed stacks of nanodots is presented, in which each nanodot is covered by a 2 nm thick SiO 2 shell. The chemical composition of these ensembles exhibits an abrupt Si/SiO 2 interface with a low amount of suboxides. A minority charge carrier lifetime of 18 μs inside of the nanodots is determined.
UR - http://www.scopus.com/inward/record.url?scp=84865350457&partnerID=8YFLogxK
U2 - 10.1007/s00339-012-6956-9
DO - 10.1007/s00339-012-6956-9
M3 - Article
AN - SCOPUS:84865350457
SN - 0947-8396
VL - 108
SP - 719
EP - 726
JO - Applied Physics A: Materials Science and Processing
JF - Applied Physics A: Materials Science and Processing
IS - 3
ER -