Quantitative determination of charge transfer parameters of photorefractive BaTiO3 : Rh from EPR-based defect studies

Optical absorption bands can be used as fingerprints of defects and their charge states in insulators and semiconductors. On the basis of the photochromicity usually shown by such materials, a method is introduced by which the optical bands are assigned to the defects and their charge states. It is...

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Bibliographic Details
Main Authors: Veber, C. (Author), Meyer, M. (Author), Schirmer, O.F (Author), Kaczmarek, M. (Author)
Format: Article
Language:English
Published: 2003-01-29.
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Online Access:Get fulltext
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100 1 0 |a Veber, C.  |e author 
700 1 0 |a Meyer, M.  |e author 
700 1 0 |a Schirmer, O.F.  |e author 
700 1 0 |a Kaczmarek, M.  |e author 
245 0 0 |a Quantitative determination of charge transfer parameters of photorefractive BaTiO3 : Rh from EPR-based defect studies 
260 |c 2003-01-29. 
856 |z Get fulltext  |u https://eprints.soton.ac.uk/15089/1/JPhys03.pdf 
520 |a Optical absorption bands can be used as fingerprints of defects and their charge states in insulators and semiconductors. On the basis of the photochromicity usually shown by such materials, a method is introduced by which the optical bands are assigned to the defects and their charge states. It is based on simultaneous measurements of the light-induced changes of the optical absorption and of the corresponding EPR signals. Moreover, indirectly optical bands of EPR-silent defects can also be labelled in this way, strongly widening the scope of EPR based defect studies. We apply this method to the infrared-sensitive photorefractive system BaTiO3:Rh, where illumination leads to recharging among the valence states Rh5+, Rh4+ and Rh3+. The values of all parameters governing the charge transfers responsible are inferred from the magnitude of the absorption bands, the absolute determination of their absorption cross-sections and the kinetics of the absorption changes under illumination. In contrast to previous investigations, these parameters are deduced independently of photorefractive measurements. 
655 7 |a Article