Light-Soaking Effects on Photoconductivity in a-Si:H Thin Films

1997 ◽  
Vol 467 ◽  
Author(s):  
E. Morgado ◽  
M. Rebelo da Silva ◽  
R. T. Henriques

ABSTRACTMetastable defects have been created by light exposure in thin films of a-Si:H. The samples have been characterized by Photothermal Deflection Spectroscopy, Electron Spin Resonance, dark- and photo-conductivity. The experimental results are consistent with numerical calculations with a recombination model involving band tails and one class of correlated dangling-bond states. The effects of light-soaking on the ligh intensity and defect density dependences of photoconductivity are reproduced by the calculations. The model allows to explain the experimental trends by changes in the electronic occupation of the gap states produced by light-induced defects.

2004 ◽  
Vol 808 ◽  
Author(s):  
J. Whitaker ◽  
J. Viner ◽  
S. Zukotynski ◽  
E. Johnson ◽  
P.C. Taylor ◽  
...  

ABSTRACTWe report the growth of tritium induced defects in tritium doped hydrogenated amorphous silicon (a-Si:H,T) as measured by electron spin resonance (ESR) and photothermal deflection spectroscopy (PDS). The measurements allow one to examine the accumulation of defects in a-Si:H,T where the defect production mechanism is known. Defects produced by tritium decay are found to be much less numerous than the number of decayed tritium atoms and they are metastable like Staebler-Wronski defects. These results provide new insight into the metastable defect creation and the role of hydrogen motion.


1998 ◽  
Vol 507 ◽  
Author(s):  
Takahiro Matsumoto ◽  
Yasuaki Masumoto ◽  
Michio Kondo

ABSTRACTThe effects of light exposure on neutral defect density at the surface of nanocrystalline Si are investigated by electron-spin resonance (ESR) experiments. A decrease of the neutral dangling bond density by light soaking was observed in this nanostructure. The reduction rate of ESR signal intensity becomes large with increasing light exposure intensity, and the reduction occurs from the excitation energy higher than 2 eV in vacuum. The reduction of the defect density can be explained in terms of the conversion of neutral states to charged states by carrier trapping.


1992 ◽  
Vol 258 ◽  
Author(s):  
M. Sebastiani ◽  
P. Fiorini ◽  
F. Alvarez ◽  
F. Pozzilli ◽  
O. Pulci ◽  
...  

ABSTRACTWe have prepared silicon carbon alloys with Tauc's gap of 2.1 eV, low defect density (≃ 3–1015cm-3) and large photoconductivity (αPhoto/αdark=105 in AM 1.5 illumination). On these samples light soaking induces a large number of metastable gap defects which are annealed out at 250 °C. We have studied the kinetics of defect formation varying the duration of light exposure and the light intensity. The experimental data are consistent with a bond breaking model (conversion of tail weak bonds into dangling bonds), provided that the actual occupation of tail states is taken into account.


1998 ◽  
Vol 507 ◽  
Author(s):  
Shenlin Chen ◽  
P. C. Taylor ◽  
J. M. Viner

ABSTRACTHydrogenated amorphous silicon alloyed with selenium has been made by plasma enhanced chemical vapor deposition (PECVD). The activation energy for electrical conduction is essentially unchanged for selenium concentrations < 1 at.%. The photo conductivity changes for selenium concentrations > 0.5 at. %. Photothermal deflection spectroscopy (PDS) and electron spin resonance (ESR), respectively, show that the width of the valence band tail states and the density of neutral silicon dangling bonds also change for selenium concentrations > 0.5 at. %.


2001 ◽  
Vol 664 ◽  
Author(s):  
Stephan Heck ◽  
Howard M. Branz

ABSTRACTWe report experimental results that help settle apparent inconsistencies in earlier work on photoconductivity and light-induced defects in hydrogenated amorphous silicon (a-Si:H) and point toward a new understanding of this subject. After observing that light-induced photoconductivity degradation anneals out at much lower T than the light-induced increase in deep defect density, Han and Fritzsche[1] suggested that two kinds of defects are created during illumination of a-Si:H. In this view, one kind of defect degrades the photoconductivity and the other increases defect sub-bandgap optical absorption. However, the light-induced degradation model of Stutzmann et al.[2] assumes that photoconductivity is inversely proportional to the dangling-bond defect density. We observe two kinds of defects that are distinguished by their annealing activation energies, but because their densities remain in strict linear proportion during their creation, the two kinds of defects cannot be completely independent.In our measurements of photoconductivity and defect absorption (constant photocurrent method) during 25°C light soaking and during a series of isochronal anneals between 25 < T < 190°C, we find that the absorption measured with E ≤1.1 eV, first increases during annealing, then exhibits the usual absorption decrease found for deeper defects. The maximum in this absorption at E ≤1.1eV occurs simultaneously with a transition from fast to slow recovery of photoconductivity. The absorption for E ≤1.1eV shows two distinct annealing activation energies: the signal rises with about 0.87 eV and falls with about 1.15 eV. The 0.87 eV activation energy roughly equals the activation energy for the dominant, fast, recovery of photoconductivity. The 1.15 eV activation energy roughly equals the single activation energy for annealing of the light-induced dangling bond absorption.


1995 ◽  
Vol 61 (2) ◽  
pp. 159-161 ◽  
Author(s):  
S. K. So ◽  
M. H. Chan ◽  
L. M. Leung

2007 ◽  
Vol 989 ◽  
Author(s):  
Tong Ju ◽  
Janica Whitaker ◽  
Stefan Zukotynski ◽  
Nazir Kherani ◽  
P. Craig Taylor ◽  
...  

AbstractThe appearance of optically or electrically induced defects in hydrogenated amorphous silicon (a-Si:H), especially those that contribute to the Staebler-Wronski effect, has been the topic of numerous studies, yet the mechanism of defect creation and annealing is far from clarified. We have been observing the growth of defects caused by tritium decay in tritiated a Si-H instead of inducing defects optically. Tritium decays to 3He, emitting a beta particle (average energy of 5.7 keV) and an antineutrino. This reaction has a half âlife of 12.5 years. In these 7 at.% tritium-doped a-Si:H samples each beta decay will create a defect by converting a bonded tritium to an interstitial helium, leaving behind a silicon dangling bond. We use ESR (electron spin resonance) and PDS( photothermal deflection spectroscopy) to track the defects. First we annealed these samples, and then we used ESR to determine the initial defect density around 1016 to 1017 /cm3 , which is mostly a surface spin density. After that we have kept the samples in liquid nitrogen for almost two years. During the two years we have used ESR to track the defect densities of the samples. The defect density increases without saturation to a value of 3x1019/cm3 after two years, a number smaller than one would expect if each tritium decay were to create a silicon dangling bond (2x1020/cm3). This result suggests that there might be either an annealing process that remains at liquid nitrogen temperature, or tritium decay in clustered phase not producing a dangling bond due to bond reconstruction and emission of the hydrogen previously paired to Si-bonded tritium atom. After storage in liquid nitrogen for two years, we have annealed the samples. We have stepwise annealed one sample at temperatures up to 200°C, where all of the defects from beta decay are annealed out, and reconstructed the annealing energy distribution. The second sample, which was grown at 150°C, has been isothermally annealing at 300 K for several months. The defects remain well above their saturation value at 300 K, and the shape of decay suggests some interaction between the defects.


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