期刊
PHYSICAL REVIEW B
卷 61, 期 3, 页码 1677-1680出版社
AMER PHYSICAL SOC
DOI: 10.1103/PhysRevB.61.1677
关键词
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Using infrared absorption (ir) spectroscopy, H evolution, and x-ray diffraction (XRD), the structure of high-H-dilution, plasma-enhanced chemical vapor deposition a-Si:H films on the edge of crystallinity is examined. From the ir Si-H wag mode peak frequency and the XRD results, we postulate the existence of very small Si crystallites contained within the as-grown amorphous matrix with the majority of the bonded H located on these crystallite surfaces. Upon annealing, a low-temperature H-evolution peak appears, and film crystallization is observed at temperatures as low as 500 degrees C, which is far below that observed for a-Si:H films grown without H dilution. While the crystallite sizes and volume fraction are too small to be detected by XRD in the as-grown films, these crystallites catalyze the crystallization of the remainder of the amorphous matrix upon annealing, enabling the evolution of H at low temperatures. The large spatial inhomogeneity in the H bonding thus produced throughout the-film is suggested to be one of the reasons for the reduced Staebler-Wronski effect observed in solar cells utilizing these films.
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