Electronic Conduction in Polymers. III. Electronic Properties of Polypyrrole

1963 ◽  
Vol 16 (6) ◽  
pp. 1090 ◽  
Author(s):  
BA Bolto ◽  
R McNeill ◽  
DE Weiss

The electron spin resonance absorption and electrical resistivity have been measured under rigorous conditions for a series of polypyrroles prepared over the temperature range 120-500�. When plotted as a function of pyrolysis temperature the resistivity shows a maximum in the region 200-300�. Although the resistivity of the polymers prepared at 120� and 500� is roughly similar, their e.s.r. behaviour is quite different. The low-temperature polymer, containing much complexed iodine, shows a very broad signal arising from an excited state probably associated with a polypyrrole-iodine charge-transfer complex; the high temperature polymer, containing no iodine, shows a strong narrow signal arising from the ground state of the polymer. The changes in conductivity of the polymers following the adsorption of electron acceptor or donor molecules have been measured. It is concluded that, depending on the relative amounts of electron donating or attracting chemisorbed species in relation to the concentration of donor nitrogen atoms in the polypyrrole, the polymer may behave as an intrinsic or extrinsic semiconductor with n- or p-type characteristics. Charge-transfer complexes of strength sufficient to cause partial ionization induce extrinsic behaviour by changing the ratio of the number of electrons to the number of holes. Substituent groups such as the hetero atoms which interact with the π-electron system inductively or through resonance affect only the relative mobility of the charge carriers and induce intrinsic behaviour.


2020 ◽  
Author(s):  
Chuanding Dong ◽  
Stefan Schumacher

<p>The mechanistic study of molecular doping of organic semiconductors (OSC) requires</p><p>an improved understanding of the role and formation of integer charge transfer complexes</p><p>(ICTC) on a microscopic level. In the present work we go one crucial step beyond</p><p>the simplest scenario of an isolated bi-molecular ICTC and study ICTCs formed of</p><p>up to two (poly[2,6-(4,4-bis(2-ethylhexyl)-4H-cyclopenta[2,1-b,3,4-b”]dithiophene)-alt-4,7-(2,1,3-</p><p>benzothiadiazole)](PCPDT-BT) oligomers and up to two CN6-CP molecules. We find that depending</p><p>on geometric arrangement, complexes containing two conjugated oligomers and two</p><p>dopant molecules can show p-type doping with double integer charge transfer, resulting in either</p><p>two singly doped oligomers or one doubly doped oligomer. Interestingly, compared to an individual</p><p>oligomer-dopant complex, the resulting in-gap states on the doped oligomers are significantly</p><p>lowered in energy. Indicating that, already in the relatively small systems studied here, Coulomb</p><p>binding of the doping-induced positive charge to the counter-ion is reduced which is an elemental</p><p>step towards generating mobile charge carriers through molecular doping.</p>



2020 ◽  
Author(s):  
Chuanding Dong ◽  
Stefan Schumacher

<p>The mechanistic study of molecular doping of organic semiconductors (OSC) requires</p><p>an improved understanding of the role and formation of integer charge transfer complexes</p><p>(ICTC) on a microscopic level. In the present work we go one crucial step beyond</p><p>the simplest scenario of an isolated bi-molecular ICTC and study ICTCs formed of</p><p>up to two (poly[2,6-(4,4-bis(2-ethylhexyl)-4H-cyclopenta[2,1-b,3,4-b”]dithiophene)-alt-4,7-(2,1,3-</p><p>benzothiadiazole)](PCPDT-BT) oligomers and up to two CN6-CP molecules. We find that depending</p><p>on geometric arrangement, complexes containing two conjugated oligomers and two</p><p>dopant molecules can show p-type doping with double integer charge transfer, resulting in either</p><p>two singly doped oligomers or one doubly doped oligomer. Interestingly, compared to an individual</p><p>oligomer-dopant complex, the resulting in-gap states on the doped oligomers are significantly</p><p>lowered in energy. Indicating that, already in the relatively small systems studied here, Coulomb</p><p>binding of the doping-induced positive charge to the counter-ion is reduced which is an elemental</p><p>step towards generating mobile charge carriers through molecular doping.</p>



1969 ◽  
Vol 47 (20) ◽  
pp. 3899-3902 ◽  
Author(s):  
S. N. Bhat ◽  
C. N. R. Rao

Electrical conductivities, electron spin resonance spectra, electronic spectra, and Seebeck coefficients of solid charge-transfer complexes of benzidine–iodine, p-phenylenediamine–iodine, and phenothiazine–iodine as well as two antimony chloride complexes of phenothiazine have been studied. The phenothiazine–I2 system shows change in sign of the majority charge carriers with the donor–acceptor ratio. The effect of ambient gases on the conductivities of a few donors, acceptors, and their complexes in the solid state have been examined. Seebeck coefficient measurements show that the conduction in TCNQ salts takes place by a hopping mechanism.





2010 ◽  
Vol 81 (15) ◽  
Author(s):  
J. T. Sun ◽  
Y. H. Lu ◽  
W. Chen ◽  
Y. P. Feng ◽  
A. T. S. Wee


1977 ◽  
Vol 55 (5) ◽  
pp. 766-770 ◽  
Author(s):  
A. W. Addison ◽  
T. H. Li ◽  
L. Weiler

The redox properties of 2,3,7,8-tetramethoxyselenanthrene and 2,3,7,8-tetramethoxythianthrene have been studied in solution in order to compare their potential applicability as charge-transfer donors. The selenium compound is the weaker reductant, yielding a stable radical cation and a reactive dication, the former dimerizing in solution. Electron spin resonance and visible absorption spectra of the stable species were obtained. The 1:1 charge-transfer complexes of the above donors with tetracyanoquinodimethane are found to be insulators.



Nature ◽  
1966 ◽  
Vol 211 (5046) ◽  
pp. 309-310 ◽  
Author(s):  
J. BRYAN JONES ◽  
MALCOLM BERSOHN ◽  
GARRY C. NIECE


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