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    Light driven photocatalytic hydrogen generation using BODIPY-thiophene-covalent organic polymers
    (Pergamon-Elsevier Science Ltd, 2025) Turgut, Ki bra; Ozdemir, Mucahit; Yildiz, Gizem; Yalcin, Bahattin; Koyuncu, Sermet; Koksoy, Baybars; Patir, Imren Hatay
    Boron-dipyrromethene (BODIPY)-based dyes have recently garnered attention as sensitizers for photocatalytic hydrogen production. They exhibit high catalytic activity through efficient electron transfer, owing to their unique properties such as high molar absorptivity, adjustable absorption and emission energies, and high fluorescence quantum efficiencies. In this study, the effect of a-OH subunit that can increase hydrophilicity on the photocatalytic hydrogen evolution in BODIPY-thiophene-based covalent organic polymers (COP) was investigated. In the conducted research, COP structures were integrated into BODIPY to enhance their light absorption capabilities, aiming to serve as photocatalysts for energy conversions under simple conditions. In the proposed system, Thiophene-BODIPY-based dyes are integrated into COP structures, where they facilitate electron excitation upon light absorption, thereby playing an effective role in photocatalytic reactions by promoting electron transfer. The photocatalyst, modified with titanium dioxide (TiO2) nanoparticles, exhibited notable performance in enhancing the efficiency of the hydrogen production process, owing to its light absorption capabilities, multifunctional fluorescent properties, and electron-accepting characteristics. The synthesized BODIPY-Th-COP-OH_TiO2 photocatalyst demonstrated higher hydrogen activity compared to BODIPY-Th-COP-CH3_TiO2, attributed to the presence of hydroxyl groups promoted hydrophilic character in the catalyst structure. Therefore, BODIPY-Th-COP-X_TiO2 photocatalysts (X: OH, CH3) utilizing methanol as sacrificial agent yielded hydrogen amounts of 0.197 mmol g-1 h-1 and 0.132 mmol g-1 h-1 for BODIPY-Th-COP-OH_TiO2 and BODIPY-Th-COP-CH3_TiO2 photocatalysts, respectively, under visible light illumination.
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    Light-Induced Performance Enhancement of Supercapacitors through Thiol-Ene Click Surface Functionalization of Thienothiophene-BODIPY Porous Polymers
    (Amer Chemical Soc, 2025) Ozdemir, Mucahit; Ulucay, Sude; Sevimli, Esra; Altinisik, Sinem; Koksoy, Baybars; Yalcin, Bahattin; Koyuncu, Sermet
    Photoassisted supercapacitors are emerging as next-generation energy storage devices that synergistically combine light harvesting and electrochemical energy storage. BODIPY-based semiconductors, known for their strong light absorption, tunable electronic properties, and photostability, have recently attracted attention as efficient photoactive components in such systems. This study investigates the potential use of cross-linked thieno[3,2-b]thiophene-BODIPY polymer as an electrode material for photoassisted supercapacitors, prepared through a surface functionalization approach using thiol-ene click chemistry. The polymer exhibited broad-band absorption and a low band gap due to extended conjugation, as confirmed by UV-vis and fluorescence spectroscopy, along with comprehensive optical, electrochemical, and morphological characterization. DFT calculations showed that the HOMO-LUMO energy gap narrows under illumination, indicating improved charge transport. Cyclic voltammetry (CV), galvanostatic charge-discharge (GCD), and electrochemical impedance spectroscopy (EIS) measurements confirmed that the cross-linked polymer offers high capacitance, low internal resistance, and long cycle stability. In terms of supercapacitor performance, a photoinduced enhancement of up to 50% in specific capacitance was observed under light. At a current density of 1.0 A/g, the specific capacitance increased from 240 F/g in the dark to 362 F/g under illumination. Stability tests conducted over 2000 cycles demonstrated that the supercapacitor retained 90% of its initial capacitance.
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    New metallophthalocyanines including benzylphenoxy groups and investigation of their organic-field effect transistor (OFET) features
    (Elsevier Sci Ltd, 2022) Ozdemir, Mucahit; Altinisik, Sinem; Koksoy, Baybars; Canimkurbey, Betul; Koyuncu, Sermet; Durmus, Mahmut; Bulut, Mustafa
    In this study, metal and metal-free novel phthalocyanines containing peripheral and non-peripheral tetra 2-ben-zylphenoxy groups were synthesized. The compounds were characterized by UV-Vis, FT-IR, H-1 NMR, and MALDI-TOF mass spectrometry as well as elemental analysis. These new phthalocyanines exhibited excellent solubility in most organic solvents, and their redox behavior was investigated in different solvents such as dimethyl sulfoxide (DMSO) and dichloromethane (DCM). The redox behavior of the peripheral and non-peripheral phthalocyanine compounds 1a -c and 2a -c was determined by cyclic voltammetry and in situ spec-troelectrochemistry. According to organic field-effect transistors (OFETs) measurements, the peripheral and non-peripheral phthalocyanine-cobalt complexes which have higher mobility than others were utilized top-gate bottom-contact OFETs fabrication. The output characteristics of the device show that its mobility is approximately 5 x 10(-2) cm(2)/Vs with p-type accumulation.