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Experimental Studies of Long-Range Atomic H Motion and Desorption in Hydrogenated Amorphous Silicon and Germanium [Thesis]

Thesis/Dissertation ·
OSTI ID:5643940
 [1]
  1. Iowa State Univ., Ames, IA (United States); Ames Laboratory (AMES), Ames, IA (United States)
Long-range H motion and desorption in low hydrogen concentration undoped hydrogenated amorphous silicon (a-Si:H) and germanium (a-Ge:H) was studied by deuterium secondary ion mass spectrometry (SIMS) depth profiles and IR absorption of a-Si:H/a-Si:(H,D)/a-Si:H and a-Ge:H/a-Ge:(H,D)/a-Ge:H. SIMS monitors deuterium motion (assumed similar to that of H), while IR yields information on hydrogen content and bonding. The diffusion constant was found to be dispersive with time, and depended on H content CH, diffusion length L, and microvoid content, at temperatures T ≤ 400 °C for a-Si:H and T ≤ 310 °C for a-Ge:H. It exhibited a power-law D(t) = Doo(ωt)–α relation in both systems. In a-Si:H, α generally deviates from the 1 – T/To dependence on the temperature T expected from a multiple trapping mechanism. The diffusion constant at constant diffusion length D(tL) then deviates from an Arrhenius dependence on the temperature. The "apparent" activation energy Ea and prefactor Do, defined by the linear best-fit of lnD(tL) vs 1/T, strongly increase with L at low CH. The Meyer-Neldel relation (MNR) Do = Aooexp(Ea/To') , where Aoo ≃ 3.1x10–14 cm2/s and To' ≃ 730 K, holds for all 1.3 ≤ Ea ≤ 2.4 eV and 2.5x10–5 ≤ Do ≤ 3100 cm2/s. In a-Ge:H, α is essentially temperature and composition independent, but increases with microvoid content. The activation energy Ea ranges from 0.7 to 1.2 eV among the various films. The Meyer-Neldel relation is observed, with Aoo ≃ 5.5x10–16 cm2/s and To' ≃ 530 K. These values are lower than the corresponging values in a-Si:H. Hydrogen desorption temperature is as low as 180 °C. Yet the significance of the MNR is questionable in both a-Si:H and a-Ge:H. The diffusion results for both a-Si:H and a-Ge:H are discussed in relation to the microstructure of the films. The nature of the microvoid-induced deep H-trapping sites is also discussed. Finally, a possible relation between the dispersive diffusion and a percolation model is presented.
Research Organization:
Iowa State Univ., Ames, IA (United States); Ames Laboratory (AMES), Ames, IA (United States)
Sponsoring Organization:
USDOE Office of Science (SC), Basic Energy Sciences (BES)
DOE Contract Number:
W-7405-ENG-82
OSTI ID:
5643940
Report Number(s):
IS-T--1559; ON: DE91016161
Country of Publication:
United States
Language:
English