Abstract :
Electrochemical studies of both the a-Si:H based metal/oxide/semiconductor structures and a-Si:H modified Pt electrode
as a part of two-electrode cell compartment with electrolyte were performed to obtain information on the nature
of mobile hydrogen in a-Si:H. We assume, that the complex formed by a hydrogen molecule and a silicon dangling bond
(the origin of Dh states) provides for mobile hydrogen. Information on the process of electron selfexchange (hopping) in
a-Si:H driven by diffusion in the presence of a concentration gradient of redox centers is obtained. The capability of the
electrochemical methods for studying the role of hydrogen in degradation of a-Si:H caused by bias annealing and/or
illumination is demonstrated. Also, it was shown that because of the unique electrocatalytic features of the a-Si:H modified
Pt electrode, the latter can act as a ‘‘programmable’’ and selective sensor of heavy metal ions and/or metal complexes.
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