Ambipolar Phototransport (mu tau e=mu tau h) Observed as an Intrinsic Property of A-SiGe:H

    Research output: Contribution to conferencePaper

    Abstract

    A study is presented of a series of high quality PECVD a-Si0.33Ge0.67 films, produced by cathodic deposition, in which small concentrations of PH3, B2H6 or air impurities were added during deposition. The quantum efficiency-mobility-lifetime product increases, and the ambipolar diffusion length (L amb) decreases monotonically with dopant concentration for both PH3 and B2H6. This result is strongevidence that for these films neither photocarrier is dominant at zero doping. This result is very different from what has been typically observed by other researchers, that the electron is the dominant photocarrier for undoped a-SiGe:H. Drive level capacitance (DLC) measurements of these alloys show an unusual behavior of being temperature-independent, and the dark conductivity activationenergy is maximum for zero doping. It is proposed that all of these unusual properties are due to the unusually low impurity concentration of these films, and that these properties are, in fact, the intrinsic properties for a-SiGe:H alloys. To verify this, films were prepared with a calibrated and controlled air leak introduced during deposition. As the air leak was increased, the filmproperties changed to typical behavior. Even for air concentrations as low as 2 ppm (gas phase), the transport measurements showed changes consistent with a shift in the Fermi level toward the conduction band.
    Original languageAmerican English
    Pages263-268
    Number of pages6
    StatePublished - 1997
    EventAmorphous and Microcrystalline Silicon Technology 1997: Materials Research Society Symposium - San Francisco, California
    Duration: 31 Mar 19974 Apr 1997

    Conference

    ConferenceAmorphous and Microcrystalline Silicon Technology 1997: Materials Research Society Symposium
    CitySan Francisco, California
    Period31/03/974/04/97

    Bibliographical note

    Work performed by Harvard University, Cambridge, Massachusetts, Boston College, Boston, Massachusetts, University of Oregon, Eugene, Oregon, and Lawrence Livermore National Laboratory, Livermore, California

    NREL Publication Number

    • NREL/CP-520-24551

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