Synthesis, characterization, and electro-optical properties of a soluble conjugated polymer containing an oxadiazole unit in the main chain

2003 ◽  
Vol 89 (10) ◽  
pp. 2618-2623 ◽  
Author(s):  
Su-Yang Zhang ◽  
Fan Kong ◽  
Rong Sun ◽  
Ren-Kuan Yuan ◽  
Xi-Qun Jiang ◽  
...  
2008 ◽  
Vol 41 (5) ◽  
pp. 1654-1662 ◽  
Author(s):  
Takayuki Iijima ◽  
Shin-ichi Kuroda ◽  
Takakazu Yamamoto

Polymers ◽  
2021 ◽  
Vol 13 (15) ◽  
pp. 2425
Author(s):  
Jiuchao Dong ◽  
Shigeki Nimori ◽  
Hiromasa Goto

A new method for fabricating conjugated polymer films was developed using electrochemical polymerization in liquid crystals and magnetic orientation. A uniaxial main chain orientation and a crosslinked network structure were achieved with this method. By employing eight types of monomers, the influence of the crosslinking for the film was investigated. The crosslinking was found to improve the solvent resistance of the conjugated polymer films. This new method is expected to be useful in various applications, such as high-powered organic electronic devices with durability.


2014 ◽  
Vol 92 (9) ◽  
pp. 1021-1025 ◽  
Author(s):  
Bandar Ali Al-Asbahi ◽  
Mohammad Hafizuddin Haji Jumali

The influence of colloidal TiO2 nanoparticle contents on the optical properties of poly (9,9′-di-n-octylfluorenyl-2,7-diyl) conjugated polymer (PFO) has been investigated. The solution blending method was used to prepare homogenous PFO/TiO2 nanocomposite. The nanocomposite films were prepared on glass substrates using the spin-coating technique. The films were divided into two groups, the first was left to dry at room temperature while the second was heat-treated at 120 °C for 1 h. Absorption and emission spectra showed that the PFO existed in α- and β-phases morphology having monomeric, excimeric, and double excimeric states. In addition, both spectra revealed that TiO2 contents and heat treatment temperature extended the conjugation length of PFO. Finally, emission spectra for both cases exhibited decreasing in the line width of zero-phonon emission spectra and increasing in the vibronic splitting energy, upon increment of the TiO2, led to a significant increase in π-electron delocalization and lower degree in chain disorder.


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