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Conjugated polymers measurements

The PES measurements arc performed with reference to the Fermi level of the photoclectron spectrometer, in solid specimens, as dealt with here, by the way the spectroscopy works. Thus, in cases when the Fermi level shifts due to some chemical modifications of the sample, i.e., in the intercalation of graphite or other layered compound [16] or in the doping of conjugated polymers 1171, il is necessary to account for the change in the Fermi energy level before interpreting spec-... [Pg.387]

Conjugated polymers are centrosymmetric systems where excited states have definite parity of even (A,) or odd (B ) and electric dipole transitions are allowed only between states of opposite parity. The ground state of conjugated polymers is an even parity singlet state, written as the 1A... PM spectroscopy is a linear technique probing dipole allowed one-photon transitions. Non linear spectroscopies complement these measurements as they can couple to dipole-forbidden trail-... [Pg.422]

Currem field characteristics measured wiih conjugated polymers sandwiched between an indium-tin oxide (ITO) anode and an aluminum cathode are usually hole dominated and are, consequently, appropriate for testing injection/lransport models for the case of unipolar current How. Data shown in Figure 12-1 refer to injection-limited currents recorded on typically 100 nm thick spin-coated films of derivatives of poly(y d/"fi-phenylenevinylene) (PPV) and a planarized poly(/ /" -pheny-leue) employing a Keilhley source measure unit. The polymers were ... [Pg.512]

Incorporation of chiral units into polymers generates optically active polymers.27 Two types of optically active polymers could be obtained according to where the chiral units reside optically active polymers with chirality derived from chiral side chains and optically active polymers with chirality derived from tire chiral main chain. The circular dichroism (CD) measurement of 32, an optically active polymer with chiral side chains, showed that the chiral substituents have induced main-chain chirality. The induced main-chain chirality disappeared at higher temperature and appeared upon cooling. This type of chiral conjugated polymer is potentially useful in reversing optical recording28 ... [Pg.479]

Preliminary measurements of electrical conductivity of the conjugated derivatives of PBTAB, PBTB and PTTB obtained by the above treatment with bromine vapor are poor semiconductors with a conductivity of the order 10 °S/cm which apparently is not due to doping. Subsequent electrochemical or chemical doping of these polymers lead to 4-6 orders of magnitude increase in conductivity. Ongoing studies of the electrical properties of these conjugated polymers with alternating aromatic/quinonoid units will be reported elsewhere. [Pg.451]

The luminance reaches 100 cd/m2 at 2.5 V with EL efficiency of 2.5 cd/ A. The corresponding external quantum efficiency is about 2% ph/el. At —10 V bias, the photosensitivity at 430 nm is around 90 mA/W, corresponding to a quantum yield of 20% el/ph [135], The carrier collection efficiency at zero bias was relatively low in the order of 10-3 ph/el. The photosensitivity showed a field dependence with activation energy of 10 2 eV [135], This value is consistent with the trap distribution measured in the PPV-based conjugated polymers [136,137],... [Pg.19]

NC Greenham, IDW Samuel, GR Hayes, RT Phillips, YARR Kessener, SC Moratti, AB Holmes, and RH Friend, Measurement of absolute photoluminescence quantum efficiencies in conjugated polymers, Chem. Phys. Lett., 241 89-96, 1995. [Pg.39]

The unique simplicity of TNT detection by this method renders the fabrication of an operable device built around amplified fluorescent polymer technology a relatively simple proposition in comparison to other technological platforms. The method relies purely on changes in fluorescence intensity. AH that is theoretically required is a means of introducing vapor samples to a conjugated polymer film, a light source to excite the polymer film, and a photodetector to measure the emission intensity as a function of time. [Pg.213]

As expected, the coordination of Pt markedly influences the photophysical characteristics of the PPE. The photoluminescence is efficiently quenched, and the absorption maximum in the visible regime experiences a hypsochromic shift. The charge-carrier mobility of different EHO-OPPE-Pt samples was determined by TOE measurements as described above for the neat EHO-OPPE. The shape of the photocurrent transients of all EHO-OPPE-Pt samples was similar to those shown in Figs. 6 and 7 for the neat EHO-OPPE. This indicates that these organometallic conjugated polymers networks are also characterized... [Pg.228]


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Polymer measurement

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