4.6 Article

Conjugated Polymers-Based Ternary Hybrid toward Unique Photophysical Properties

期刊

MOLECULES
卷 27, 期 20, 页码 -

出版社

MDPI
DOI: 10.3390/molecules27207011

关键词

F8; MEH-PPV; optical and optoelectronic properties; OLED

资金

  1. National Plan for Science, Technology and Innovation (MAARIFAH), King Abdulaziz City for Science and Technology, Kingdom of Saudi Arabia [2-17-01-001-0037]

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Blending three different polymers in optimal ratio can improve their optical and optoelectronic properties. One of the blends showed the best performance in terms of current and turn-on voltage.
The improvement of optical and optoelectronic properties of the individual poly [2-methoxy-5- (2-ethylhexyloxy)-1,4-phenylenevinylene] (MEH-PPV), poly[2-methoxy-5-(3,7-dimethyl-octyloxy)-1,4-phenylenevinylene]-End capped with Dimethyl phenyl (OC1C10-PPV-DMP), and poly (9,9 '-di- n -octylfluorenyl-2,7-diyl) (F8) was revealed by blending them in ternary hybrid with optimal ratio (F8/2 wt.% MEH-PPV/2 wt.% OC1C10-PPV-DMP). All individual and optimal ternary solutions were prepared via the solution-blending method followed by depositing them onto glass and ITO substrates using spin-coating technique. The semi-crystalline phase of the ternary hybrid and the strong mixing between the conjugated polymers were evidenced by observing the X-ray diffraction patterns that related to F8 into the hybrid diffractogram. The optical and optoelectronic properties of all prepared thin films were investigated in terms of absorption and emission spectra, Commission International d ' Eclairage (CIE) coordinates, and current-voltage (I-V) characterizations. Emission peaks at the entire range of visible spectrum can be revealed from the ternary hybrid of the three individual conjugated polymers, producing white emission as evidenced from the emission spectrum and CIE coordinates of the hybrid. Among all fabricated organic light-emitting diodes (OLEDs) devices, the ternary hybrid-based-OLED revealed the best performance in terms of current and turn-on voltage.

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