Polymeric compositions having near IR photoconduction

Peculiar properties of carrier photogeneration in the polymer compositions based on polystyrene containing substituted tetrathiafulvalenes – electron donors, 2,4,5,7-tetranitro-9-fluorenone – acceptor of electrons, cationic polymethine dye – tetrafluoroborate 1,3,3-trimethy 1-2-[3-(1,3-dihydro-1,3,3...

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Дата:2004
Автори: Davidenko, N.A., Kuvshinsky, N.G., Melenevsky, D.A., Derevyanko, N.A., Ishchenko, A.A., Kulinich, A.V., Neilands, O., Plotniece, M.
Формат: Стаття
Мова:English
Опубліковано: Інститут фізики напівпровідників імені В.Є. Лашкарьова НАН України 2004
Назва видання:Semiconductor Physics Quantum Electronics & Optoelectronics
Онлайн доступ:http://dspace.nbuv.gov.ua/handle/123456789/118179
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Назва журналу:Digital Library of Periodicals of National Academy of Sciences of Ukraine
Цитувати:Polymeric compositions having near IR photoconduction / N.A. Davidenko, N.G. Kuvshinsky, D.A. Melenevsky, N.A. Derevyanko, A.A. Ishchenko, A.V. Kulinich, O. Neilands, M. Plotniece // Semiconductor Physics Quantum Electronics & Optoelectronics. — 2004. — Т. 7, № 2. — С. 217-221. — Бібліогр.: 9 назв. — англ.

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Digital Library of Periodicals of National Academy of Sciences of Ukraine
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spelling irk-123456789-1181792017-05-30T03:05:13Z Polymeric compositions having near IR photoconduction Davidenko, N.A. Kuvshinsky, N.G. Melenevsky, D.A. Derevyanko, N.A. Ishchenko, A.A. Kulinich, A.V. Neilands, O. Plotniece, M. Peculiar properties of carrier photogeneration in the polymer compositions based on polystyrene containing substituted tetrathiafulvalenes – electron donors, 2,4,5,7-tetranitro-9-fluorenone – acceptor of electrons, cationic polymethine dye – tetrafluoroborate 1,3,3-trimethy 1-2-[3-(1,3-dihydro-1,3,3-trimethyl-2I-2-indolyliden)-1-propenyl]-3I-indolium and neutral merocyanine - 5-[6-(1,3-dihydro[1,3,3-trimethyl-2I-indol-2-yliden)-4-phenyl-3,5-(ethylene)-hexa-2,4,6-trien-1-yl] thiobarbituric acid – sensitizers. The photoconductivity in the dye absorption range increases, when the cation dye changed to the neutral, mostly due to mobile carrier with both charges sign photogeneration, and the activation energy of the photoconductivity current decrease. The decrease of photoconduction current activation energy can be related to the organic charged counterion generation in the neutral dye case, and the uncoloured counterion retains more strongly the opposite charge on the photogenerated organic ion in the cation dye case. 2004 Article Polymeric compositions having near IR photoconduction / N.A. Davidenko, N.G. Kuvshinsky, D.A. Melenevsky, N.A. Derevyanko, A.A. Ishchenko, A.V. Kulinich, O. Neilands, M. Plotniece // Semiconductor Physics Quantum Electronics & Optoelectronics. — 2004. — Т. 7, № 2. — С. 217-221. — Бібліогр.: 9 назв. — англ. 1560-8034 PACS: 79.60.Jv http://dspace.nbuv.gov.ua/handle/123456789/118179 en Semiconductor Physics Quantum Electronics & Optoelectronics Інститут фізики напівпровідників імені В.Є. Лашкарьова НАН України
institution Digital Library of Periodicals of National Academy of Sciences of Ukraine
collection DSpace DC
language English
description Peculiar properties of carrier photogeneration in the polymer compositions based on polystyrene containing substituted tetrathiafulvalenes – electron donors, 2,4,5,7-tetranitro-9-fluorenone – acceptor of electrons, cationic polymethine dye – tetrafluoroborate 1,3,3-trimethy 1-2-[3-(1,3-dihydro-1,3,3-trimethyl-2I-2-indolyliden)-1-propenyl]-3I-indolium and neutral merocyanine - 5-[6-(1,3-dihydro[1,3,3-trimethyl-2I-indol-2-yliden)-4-phenyl-3,5-(ethylene)-hexa-2,4,6-trien-1-yl] thiobarbituric acid – sensitizers. The photoconductivity in the dye absorption range increases, when the cation dye changed to the neutral, mostly due to mobile carrier with both charges sign photogeneration, and the activation energy of the photoconductivity current decrease. The decrease of photoconduction current activation energy can be related to the organic charged counterion generation in the neutral dye case, and the uncoloured counterion retains more strongly the opposite charge on the photogenerated organic ion in the cation dye case.
format Article
author Davidenko, N.A.
Kuvshinsky, N.G.
Melenevsky, D.A.
Derevyanko, N.A.
Ishchenko, A.A.
Kulinich, A.V.
Neilands, O.
Plotniece, M.
spellingShingle Davidenko, N.A.
Kuvshinsky, N.G.
Melenevsky, D.A.
Derevyanko, N.A.
Ishchenko, A.A.
Kulinich, A.V.
Neilands, O.
Plotniece, M.
Polymeric compositions having near IR photoconduction
Semiconductor Physics Quantum Electronics & Optoelectronics
author_facet Davidenko, N.A.
Kuvshinsky, N.G.
Melenevsky, D.A.
Derevyanko, N.A.
Ishchenko, A.A.
Kulinich, A.V.
Neilands, O.
Plotniece, M.
author_sort Davidenko, N.A.
title Polymeric compositions having near IR photoconduction
title_short Polymeric compositions having near IR photoconduction
title_full Polymeric compositions having near IR photoconduction
title_fullStr Polymeric compositions having near IR photoconduction
title_full_unstemmed Polymeric compositions having near IR photoconduction
title_sort polymeric compositions having near ir photoconduction
publisher Інститут фізики напівпровідників імені В.Є. Лашкарьова НАН України
publishDate 2004
url http://dspace.nbuv.gov.ua/handle/123456789/118179
citation_txt Polymeric compositions having near IR photoconduction / N.A. Davidenko, N.G. Kuvshinsky, D.A. Melenevsky, N.A. Derevyanko, A.A. Ishchenko, A.V. Kulinich, O. Neilands, M. Plotniece // Semiconductor Physics Quantum Electronics & Optoelectronics. — 2004. — Т. 7, № 2. — С. 217-221. — Бібліогр.: 9 назв. — англ.
series Semiconductor Physics Quantum Electronics & Optoelectronics
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AT derevyankona polymericcompositionshavingnearirphotoconduction
AT ishchenkoaa polymericcompositionshavingnearirphotoconduction
AT kulinichav polymericcompositionshavingnearirphotoconduction
AT neilandso polymericcompositionshavingnearirphotoconduction
AT plotniecem polymericcompositionshavingnearirphotoconduction
first_indexed 2023-10-18T20:31:33Z
last_indexed 2023-10-18T20:31:33Z
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