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Citation - WoS: 8
Citation - Scopus: 9
Tuning the Colour of Solution Processed Perylene Tetraester Based Oleds From Yellowish-Green To Greenish-White: a Molecular Engineering Approach
(Elsevier, 2023) Aksoy, Erkan; Bozkuş, Volkan; Varlıklı, Canan
Three regioisomericaly pure 1,7-di-ethynyl bridged perylene-3,4,9,10-tetracarboxy tetrabutylesters functionalized with triisopropylsilyl-ethynylen (PTE1), phenyl-ethynylen (PTE2) and tetraphenylsilyl-ethynylen (PTE3) groups were synthesized. Photophysical, thermal, electrochemical, and solution processed electroluminescence (EL) behaviours were investigated in comparison with a basic perylene-3,4,9,10-tetracarboxy tetrabutylester (PTEref) structure. Stepwise π conjugation, allowed tuning the absorption and photoluminescence wavelengths of the PTEs without disturbing the photo, thermal and electrochemical stabilities; ≫10h, >250 °C, and >50 cycles, respectively. Electron mobility of PTE2 is measured to be more than 10-fold of the other PTE derivatives. Individual utilization of PTE derivatives as solid-state emitters in poly(N-vinylcarbazole) (PVK): 2-(4-Biphenylyl)-5-phenyl-1,3,4-oxadiazole (PBD) host matrix produced yellowish-green EL. Benefiting from higher electron mobiliy, PTE2 emitter presented the best device efficiency values with an EL maximum of 535 nm. Whereas dual doping of the synthesized PTEs with PTEref resulted in greenish-white light with increased stability. Although the emitting layer contained no red emitting component, optimization of the dual doping ratio of PTEref:PTE3 produced a colour rendering index value of 76 with Commission Internationale d'Eclairage coordinates of (0.29, 0.37).
Citation - WoS: 6
Citation - Scopus: 6
Photocatalytic Activity of Dye-Sensitized and Non-Sensitized Go-Tio2 Nanocomposites Under Simulated and Direct Sunlight
(Wiley-Blackwell, 2022) İlhan, Hatice; Durmaz Çaycı, Gamze Belkis; Aksoy, Erkan; Diker, Halide; Varlıklı, Canan
Graphene oxide (GO), amine-modified graphene oxide (mGO), and N-TiO2 composites were synthesized by low-temperature hydrothermal method and characterized by using X-ray diffraction, X-ray photoelectron spectroscopy, FTIR, and BET analysis techniques. The films of synthesized TiO2, mGO:TiO2, N-TiO2, GO:TiO2, GO:N-TiO2, and commercially available P25 were prepared by doctor blade method. These films and their perylene-3,4,9,10-tetracarboxy tetrabutylester (PTE)-sensitized forms were employed as photocatalysts for the photodegradation of rhodamine-B (RhB) under Xe lamp and direct sunlight irradiations. Independent from the irradiation source, the photocatalytic order of the non-sensitized films were GO:N-TiO2 > GO:TiO2 > N-TiO2 > mGO:TiO2 > TiO2 > P25, but seven and 15 folds of increments were detected under direct sunlight irradiation. PTE-sensitized catalyst films exhibited more than two folds of increase in the photocatalytic rate constants compared to their non-sensitized counterparts under Xe lamp irradiation. Under direct sunlight irradiation no matter which photocatalyst was used, the photocatalytic activity of these films was enhanced seven folds. Reusability tests revealed no significant changes in the photocatalytic rate constants obtained with both the non-sensitized and sensitized films.
Citation - WoS: 9
Citation - Scopus: 11
White Led Light Production Using Dibromoperylene Derivatives in Down Conversion of Energy
(Canadian Science Publishing, 2018) Aksoy, Erkan; Demir, Nuriye; Varlıklı, Canan
Perylene derivatives of N,N′-bis(2,6-diisopropylphenyl)-1,6(7)-dibromoperylene-3,4,9,10-tetracarboxylic diimide (DBrPDI) and 1,7-dibromo perylene-3,4,9,10-tetracarboxylic acid butyl ester (DBrPTE) were synthesized, and their structural and optical characterizations were explored. Both DBrPDI and DBrPTE, which were utilized as wavelength converters on a GaN/InGaN based blue LED, were singlet sensitizers and had molar absorptivity constants around 104 Lmol-1cm-1. The blue LED that was used had Commission internationale de l'eclairage (CIE) coordinates of x, y = 0.13, 0.06; power and luminous efficiencies of 2.7 lm/W and 6.6 cd/A @5 mA, respectively. Because the fluorescence quantum yield of DBrPDI was much higher than that of DBrPTE, a meaningful white light efficiency was obtained with the diimide derivative. The use of DBrPDI resulted in white light with CIE coordinates of x, y = 0.34, 0.29 and luminous efficiency of 6.35 cd/A @5 mA, respectively. Using DBrPDI in a resin matrix resulted in more than three orders of magnitude increase in the luminous efficiency value (23.0 cd/A @5 mA) while the CIE coordinates remained the same. Whenever the applied current reached 20 mA, a CRI value of Ra = 90 was obtained.

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