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      This book is the result of direct and indirect cooperation of colleagues from Brazil and all over the world who have contributed with their experience, work and advice, as well as graduate students working on their theses under my direction, or just spending some time at my laboratory at the State University of Campinas, Campinas‐SP, Brazil.

      My warm acknowledgments to all of them:

Araújo, William R. Arizmendi, Luis
Barbosa, Marcelo C. Bassewitz, J.P.
Bian, Shaopin Buse, Karsten
Carrascosa, Mercedes Capovilla, Danilo
Carvalho, Jesiel F. Cescato, Lucila H.
Freschi, Agnaldo A. Garcia, Paulo Magno
Hernandes, Antonio C. Inocente Junior, Nilson R.
Kamenov, V.P. Kamshilin, Alexei A.
Kip, Detlef Klein, Marvin
Krätzig, Eckhard Kulikov, V.V.
Kumamoto, R. Launay, Jean Claude
Longeaud, Christophe Lorduy G., Hector
Montegegro, Renata Mosquera, Luis
Oliveira, Ivan de Odoulov, S.G.
Prokofiev, Victor V. Rasnik, Ivan
Ringhofer, Klaus H.
Rupp, Romano A.
Salazar, A. Santos, Paulo Acioly Marques dos
Santos, Pedro Valentim dos Santos, Tatiane Oliveira dos
Schamonina, Ekaterina Shcherbin, K.V
Shumelyuk, A. Stepanov S.I.
Sugg, Bertrand Sturman, B.I.
Telles, A.C. Troncoso, L.S.

Image described by caption.

      Figure 1 Naturally birefringent uniaxial lithium niobate crystal view under converging white light between crossed polarizers with its c‐axis (optical axis) laying perpendicular to the plane (upper) and on the plane (lower).

      Introduction

      In the case of photorefractive materials, the light excites charge carriers from Localized States (LS‐photoactive centers) in the forbidden Band Gap (BG) to Extended States (conduction or valence bands) where they move, are retrapped and excited again and so on. During this process, the charge carriers progressively accumulate in the darker regions of the sample. In this way, charges of one sign accumulate in the darker regions while leaving charges of the opposite sign in the brighter regions. This spatial modulation of charges produces an associated space‐charge electric field. The combination of both effects gives rise to the so‐called photorefractive effect: the light produces a photoconductive‐based electric field spatial modulation that in turn produces an index‐of‐refraction modulation via the electro‐optic effect. This change can be reversed by the action of light or by relaxation even in the dark.

      The action of light on a photosensitive material may produce changes in the electrical polarizability of the molecules and by this means a change in the complex index‐of‐refraction will result. This change may be sensible or not, depending on the wavelength spectral range analyzed. The imaginary part of the index (the extinction coefficient, related to absorption) or the real part (the so‐called “index‐of‐refraction” itself) may be more affected when observed in a certain wavelength spectral range. This is the case of dyes, some silver salts, chalcogenic glasses, photoresists and other materials. When sensible changes occur in the real part of the complex index of refraction, these materials are also called “photorefractives” because they actually show changes in the real refractive index under the action of light. These changes can be reversible or not. What is the essential difference between these processes and those we have mentioned before and we are dealing with in this book? The difference is that the latter always involve the establishment of a space‐charge electric field and the production of index‐of‐refraction changes via an electro‐optic (or Pockels) effect. We should therefore rather call them “photo‐electro‐refractive” materials instead of just using the “photorefractive” label. However, the latter generic name is so widespread nowadays in the scientific literature that it would be hard to change it now. In this book, we shall therefore only use the term “photorefractive”, but the reader should be aware that materials of a different nature are usually referred to under this same label.

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