Scopus İndeksli Yayınlar Koleksiyonu / Scopus Indexed Publications Collection
Permanent URI for this collectionhttps://hdl.handle.net/11147/7148
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Article Citation - WoS: 2Citation - Scopus: 2Investigation on the Keggin Anchored on Hydroxide-Functionalized Single-Walled Carbon Nanotubes as Superior Cathode for Aqueous Zinc-Ion Batteries(American Chemical Society, 2025) Chilufya, Langson; Sertbaş, Vahide; Aytekin, Ahmet; Karabudak, Engin; Emirdag-Eanes, MehtapRechargeable aqueous zinc-ion batteries (AZIBs) have become a viable option in electrochemical energy storage systems (EESS) owing to their inherent safety features and economic friendliness. Nonetheless, creating suitable cathode materials for AZIBs with high structural stability, good rate performance, and great capacity remains a significant challenge. Polyoxometalate (POM)-based nanohybrid materials have shown promising results in high cycling stability and great specific capacity. However, POMs susceptible to electrolyte dissolution and the sluggish Zn-ion (Zn2+) kinetics have significantly hampered their electrochemical performance as cathodes for AZIBs. Herein, we present a Keggin POM, K<inf>3</inf>[PW<inf>12</inf>O<inf>40</inf>]·nH<inf>2</inf>O (KPW<inf>12</inf>), anchored on hydroxyl (OH)-functionalized single-walled carbon nanotubes (SWOH) that were fabricated via a facile ultrasonication procedure. Employed as cathodes for AZIBs, the optimal KPW<inf>12</inf>/SWOH feature exhibited remarkable electrochemical performance. The system satisfied the Zn2+storage, achieving a reversible discharge capacity of 183 mAh g–1at a high current density of 5C with a flat and long discharge plateau after 160 cycles. The perfect synergistic contribution of the pseudocapacitive nature of the super-reduced state of KPW<inf>12</inf>and the electron-conductive network of SWOH was attributed to this exceptional electrochemical performance. Furthermore, the presence of oxygen in SWOH enhanced the transfer kinetics of electrons and smooth Zn2+diffusion while lowering the Zn2+migration energy barrier by providing more accessible active sites. This demonstrates remarkable promise in fabricating robust electrode materials optimized for integration within aqueous battery systems that pave the way for further research into POM-based materials for EESS. © 2025 Elsevier B.V., All rights reserved.Article Citation - WoS: 4Citation - Scopus: 5Mini-Review: "ball-Type Phthalocyanines": Similarities and Differences From Mono Phthalocyanines(Bentham Science Publishers, 2019) Göl, Emre Yusuf; Karabudak, EnginBall-type phthalocyanines are recently synthesized binuclear derivatives of the widely known phthalocyanine molecule. In the ball-type Pc molecule, two cofacially arranged Pc rings have four bridged substituents on the peripheral positions of benzenes. Due to their cofacially arranged phthalocyanine rings and, strong intramolecular and intermolecular interactions, ball-type phthalocyanines have different properties than their parent molecule and these structures have many potential application areas. This review describes three different synthesis methods of ball-type phthalocyanines; synthesis in the solvent, synthesis in solid, and synthesis under microwave irradiation. The synthesis that occurs in the shortest time with the highest yield is the synthesis in the solid phase. General differences between a ball-type phthalocyanine and a monophthalocyanine, such as differences in electronic spectra and effects of cofacial arrangement and central metal atoms, are also discussed. The shape of the Q-bands indicates the differences in electronic spectra. In ball-type Pcs, the Q-bands are broad and have poor resolution. Some potential applications, such as gas sensors, NLO devices, potential usage in photodynamic therapy and artificial photosynthesis of ball-type phthalocyanines are also mentioned. Ball-type Pcs can be used as a sensor for gases such as; CO2, CO, SO2, VOC. A novel water-soluble ball-type Pc may have potential application in PDT. Finally, we consider future prospects of these molecules.