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Permanent URI for this collectionhttps://hdl.handle.net/20.500.14288/3
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Publication Metadata only Stepwise conversion of methane to methanol over Cu-mordenite prepared by supercritical and aqueous ion exchange routes and quantification of active Cu species by H2-TPR(Elsevier, 2023) Sushkevich, Vitaly; van Bokhoven, Jeroen A.; Department of Chemical and Biological Engineering; Yousefzadeh, Hamed; Bozbağ, Selmi Erim; Erkey, Can; Department of Chemical and Biological Engineering; Koç University Tüpraş Energy Center (KUTEM) / Koç Üniversitesi Tüpraş Enerji Merkezi (KÜTEM); College of EngineeringCopper-exchanged mordenite prepared by supercritical ion exchange (SCIE) and aqueous ion exchange (AIE) were investigated in stepwise conversion of methane to methanol. Increasing the oxygen activation temperature and methane reaction time enhances the methanol yield of copper-exchanged mordenite prepared by SCIE (CuMORS). The reducibility of Cu-MORS was compared with those of Cu-MORA prepared by aqueous ion exchange (AIE) using H-2-TPR. It was demonstrated for the first time that deconvoluted H2-TPR profile coupled with effects of Cu loading and oxygen activation temperature on methanol yield data can be used to distinguish the active Cu sites from inactive ones based on their reduction temperature. The copper species responsible for methane activation were found to be reduced below 150 C by H-2 in both Cu-MORS and Cu-MORA. From the stoichiometry of the reaction of H-2 with Cu2+ species, the average number of copper atoms of active sites were calculated as 2.07 and 2.80 for Cu-MORS and Cu-MORA, respectively. Differences in structure of copper species caused by the synthesis routes were also detected by in-situ FTIR upon NO adsorption indicating a higher susceptibility of CuMORS towards autoreduction. The results demonstrated the potential of TPR based methods to identify copper active sites and suggested the importance of site selective ion exchange in order to controllably synthesize active Cu species in zeolites.Publication Metadata only Solar-light-driven photocatalytic hydrogen evolution activity of gCN/WS2 heterojunctions incorporated with the first-row transition metals(Elsevier Science Sa, 2023) Acar, Eminegul Genc; Aslan, Emre; Patir, Imren Hatay; Department of Chemistry; Yılmaz, Seda; Eroğlu, Zafer; Metin, Önder; Department of Chemistry; Koç University Tüpraş Energy Center (KUTEM) / Koç Üniversitesi Tüpraş Enerji Merkezi (KÜTEM); Koç University Surface Science and Technology Center (KUYTAM) / Koç Üniversitesi Yüzey Teknolojileri Araştırmaları Merkezi (KUYTAM); Graduate School of Sciences and Engineering; College of SciencesThe design of semiconductor-based heterojunctions is an effective strategy to build highly active photo-catalyst systems. In this study, tungsten disulfide (WS2) modified graphitic carbon nitride (gCN) hetero-junction (gCN/WS2) is incorporated with Co and Ni (gCN/WS2-Co and gCN/WS2-Ni) to enhance the photocatalytic hydrogen evolution reaction (HER) activity of gCN/WS2 via performing a chemical reduction method and characterized by advanced analytical techniques. The photocatalytic HER activities of gCN, gCN/ WS2, gCN/WS2-Ni and gCN/WS2-Co were measured as 0.126, 0.221, 0.237 and 0.249 mmol g-1h-1, respec-tively, under the visible light irradiation. The improvement of photocatalytic activity and stability of gCN/ WS2-Ni and gCN/WS2-Co nanocomposites could be attributed to the 2D/2D heterojunction structure, ex-tended light harvesting ability, increased electron-hole lifetime and decreased recombination rate of the charge carriers. Moreover, mechanistic studies revealed that a S-scheme heterojunction is attributed to the enhanced photocatalytic HER by the gCN/WS2-Ni and gCN/WS2-Co photocatalysts, which provides pro-moted efficiency by photocarrier transfer and separation.Publication Metadata only Black phosphorus/WS2-TM (TM: Ni, Co) heterojunctions for photocatalytic hydrogen evolution under visible light illumination(MDPI, 2023) Acar, Emineguel Genc; Çekceoglu, Ilknur Aksoy; Aslan, Emre; Patir, Imren Hatay; Department of Chemistry; Yılmaz, Seda; Eroğlu, Zafer; Metin, Önder; Department of Chemistry; Koç University Tüpraş Energy Center (KUTEM) / Koç Üniversitesi Tüpraş Enerji Merkezi (KÜTEM); Koç University Surface Science and Technology Center (KUYTAM) / Koç Üniversitesi Yüzey Teknolojileri Araştırmaları Merkezi (KUYTAM); Graduate School of Sciences and Engineering; College of SciencesBlack phosphorus (BP) has recently emerged as a versatile photocatalyst owing to its unique photophysical properties and tunable bandgap. Nonetheless, the rapid recombination of the photogenerated charges of pristine BP samples has significantly hindered its practical applications in photocatalysis. Herein, we report, for the first time, the effect of transition metal nanoparticles (Ni and Co) as co-catalysts on the photocatalytic activity of BP/tungsten disulfide (WS2) binary heterojunctions (BP/WS2-TM (TM: Ni, Co)) in the hydrogen evolution reaction (HER) under visible light irradiation (& lambda; > 420 nm). Ternary heterojunctions named BP/WS2-TM (TM: Ni, Co) were synthesized via a chemical reduction method, leading to the formation of an S-scheme heterojunction, in which BP acts as a reduction catalyst and WS2 serves as an oxidation catalyst. BP/WS2-Ni and BP/WS2-Co performed substantial amounts of hydrogen generation of 9.53 mmol h(-1)g(-1) and 12.13 mmol h(-1)g(-1), respectively. Moreover, BP/WS2-Co exhibited about 5 and 15 times higher photocatalytic activity compared to the binary BP/WS2 heterojunctions and pristine BP, respectively. The enhanced photocatalytic activity of the heterojunction catalysts is attributed to the extended light absorption ability, enhanced charge separation, and larger active sites. This study is the first example of photocatalytic hydrogen evolution from water by using Ni- and Co-doped binary BP/WS2 heterojunctions.Publication Metadata only Exploration of novel 6,8,9-trisubstituted purine analogues: synthesis, in vitro biological evaluation, and their effect on human cancer cells(Tubitak Scientific & Technological Research Council Turkey, 2024) Polat, Muhammed Fatih; Atalay, Rengul; Tuncbilek, Meral; N/A; Şahin, İrem Durmaz; Koç University Research Center for Translational Medicine (KUTTAM); School of MedicineCancer, a leading global cause of mortality, demands continuous advancements in therapeutic strategies. This study focuses on the design and synthesis of a novel series of purine derivatives, specifically 6 -(substituted phenyl piperazine)-8-(4-phenoxyphenyl)9-cyclopentyl purine derivatives (5-11). The motivation behind this endeavor lies in addressing acquired resistance mechanisms in cancer cells, a significant hurdle in current treatment modalities. The synthesis, starting from 4,6-dichloro-5-nitropyrimidine, involves a multi -step process, resulting in seven new purine derivatives. Biological evaluation against human liver, colon, and breast cancer cells (Huh7, HCT116, and MCF7, respectively) was performed using the SRB assay. Among the synthesized analogs, compounds 5 and 6, exhibited notable cytotoxic activity, surpassing clinically used positive controls 5-Fluorouracil and Fludarabine in terms of efficacy. This research underscores the potential of purine derivatives with a phenyl group at the C-8 position as a scaffold for developing compounds with improved anticancer properties. The findings offer insights for future exploration and development of novel agents in cancer pharmaceutical research.Publication Metadata only Stabilization and adiabatic control of antiferromagnetically coupled skyrmions without the topological hall effect(Royal Soc Chemistry, 2023) Department of Electrical and Electronics Engineering; Yağan, Rawana; Cheghabouri, Arash Mousavi; Onbaşlı, Mehmet Cengiz; Department of Electrical and Electronics Engineering; Graduate School of Sciences and Engineering; College of EngineeringSynthetic antiferromagnetically coupled (SAF) multilayers provide different physics of stabilizing skyrmions while eliminating the topological Hall effect (THE), enabling efficient and stable control. The effects of material parameters, external current drive, and a magnetic field on the skyrmion equilibrium and propagation characteristics are largely unresolved. Here, we present a computational and theoretical demonstration of the large window of material parameters that stabilize SAF skyrmions determined by saturation magnetization, uniaxial anisotropy, and Dzyaloshinskii-Moriya interaction. Current-driven SAF skyrmion velocities reach & SIM;200 m s(-1) without the THE. The SAF velocities are about 3-10 times greater than the typical ferromagnetic skyrmion velocities. The current densities needed for driving SAF skyrmions could be reduced to 10(8) A m(-2), while 10(11) A m(-2) or above is needed for ferromagnetic skyrmions. By reducing the SAF skyrmion drive current by 3 orders, Joule heating is reduced by 6 orders of magnitude. These results pave the way for new SAF interfaces with improved equilibrium, dynamics, and power savings in THE-free skyrmionics.Publication Metadata only Active sites and their individual turnover frequencies for ethylene hydrogenation on reduced graphene aerogel(Amer Chemical Soc, 2024) Department of Chemistry;Department of Chemical and Biological Engineering; Yalçın, Kaan; Öztulum, Samira Fatma Kurtoğlu; Öztuna, Feriha Eylül Saraç; Kanat, Gizem Hasibe; Ünal, Uğur; Uzun, Alper; Koç University Tüpraş Energy Center (KUTEM) / Koç Üniversitesi Tüpraş Enerji Merkezi (KÜTEM); Koç University Surface Science and Technology Center (KUYTAM) / Koç Üniversitesi Yüzey Teknolojileri Araştırmaları Merkezi (KUYTAM); Graduate School of Sciences and Engineering; College of Sciences; College of EngineeringGraphene aerogel (GA) was reduced at various temperatures to prepare a series of reduced graphene aerogels (rGAs) with different surface characteristics. Detailed characterization demonstrated that an increase in the thermal reduction temperature leads to an increase in surface area accompanied by an increase in surface density of defect sites formed by the removal of the oxygen-containing functional groups. rGA samples were then tested for ethylene hydrogenation under identical conditions. A comparison of catalytic performances of each catalyst demonstrated that the rGA sample prepared by reduction in Ar at 900 degrees C (rGA-900) provides the highest performance compared with others prepared at lower temperatures. Next, we analyzed the per-gram activity of each catalyst as a sum of individual contributions from different defect sites quantified by Raman spectroscopy and CHNS-O analysis to determine the individual turnover frequencies (TOFs) of each active site. This analysis identified polyene-like structures and interstitial defects associated with amorphous sp(2) bonded carbon atoms as the dominant active sites responsible for hydrogenation. A comparison of their TOFs further indicated that the polyene-like structures provide approximately ten times higher TOF compared to those associated with the amorphous carbon defects. These results, identifying the dominant active centers and quantifying their corresponding TOFs, provide opportunities toward the rational design of GA-based carbocatalysts.Publication Metadata only Step-edge decoration and clustering of Pt atoms on a Cu(211) stepped surface(Amer Chemical Soc, 2024) Department of Chemistry; Mohammadpour, Amin; Kaya, Sarp; Department of Chemistry; Koç University Tüpraş Energy Center (KUTEM) / Koç Üniversitesi Tüpraş Enerji Merkezi (KÜTEM); Graduate School of Sciences and Engineering; College of SciencesThe atomic manipulation of the low-coordination sites of metal catalysts can give rise to activity enhancement;however, it is rather challenging to locally probe the dynamic changes and activities of these sites. Herein, step-edge/terrace site decoration and site exchange of Pt atoms with a stepped Cu(211) surface were investigated by a combination of infrared reflection absorption spectroscopy (IRRAS) and temperature-programmed desorption (TPD) of carbon monoxide (CO). For a low coverage of Pt, step decoration and site exchange with Cu were found to be two pathways to isolate Pt as single atoms. CO preferentially adsorbs near the Cu step sites on the lower terrace, and the binding energies of CO show strong Pt coverage dependence. The presence of Pt on terrace and step sites modifies the binding energy of CO absorbed on Cu in the proximity. Increased Pt-Pt lateral coordination changes the site preference;however, the reduced binding energy of CO to Pt is attributed to heteroatom bond formation rather than the strain induced by the lattice mismatch.Publication Metadata only Accelerating water oxidation on BiVO4 photoanodes via surface modification with Co dopants(Royal Soc Chemistry, 2023) Osterbacka, Nicklas; Erdem, Emre; Wiktor, Julia; Department of Physics;Department of Chemistry; Barzgarvishlaghi, Mahsa; Kahraman, Abdullah; Usman, Emre; Sennaroğlu, Alphan; Kaya, Sarp; Koç University Tüpraş Energy Center (KUTEM) / Koç Üniversitesi Tüpraş Enerji Merkezi (KÜTEM); Koç University Surface Science and Technology Center (KUYTAM) / Koç Üniversitesi Yüzey Teknolojileri Araştırmaları Merkezi (KUYTAM); Graduate School of Sciences and Engineering; College of SciencesDespite the vast investigations on improving the photoelectrochemical performance of BiVO4 for water splitting, charge recombination in the near-surface region remains a challenge. In this study, we showed that the diffusion of Co2+ ions into the BiVO4 subsurface boosted the water oxidation activity and charge injection efficiency remarkably. The increase in the concentration of oxygen vacancies upon the incorporation of cobalt ions was shown by electron paramagnetic resonance (EPR) spectroscopy and confirmed by density functional theory (DFT) calculations. DFT calculations revealed that vanadium sites in the subsurface region were the most favorable sites for substitution with cobalt ions. Charge localization at surface oxygen vacancies was found less favorable in the presence of cobalt in the subsurface layer, eliminating surface recombination. This resulted in 4.25 times larger charge injection efficiency and 6.2 times higher photocurrent density at the potential of & SIM;0.6 V, as compared to pristine BiVO4. This enhancement was significantly larger as compared to CoOx-loaded BiVO4, indicating that the suppressed recombination at the surface and improved charge transfer kinetics obtained solely by CoOx deposition are not sufficient for enhanced activity of BiVO4. A longer charge carrier lifetime obtained upon cobalt incorporation was observed by transient absorption spectroscopy and verified the reduced rate of recombination.Publication Metadata only High-throughput computational screening of MOF adsorbents for efficient propane capture from air and natural gas mixtures(AIP Publishing, 2024) Department of Chemical and Biological Engineering; Erçakır, Göktuğ; Aksu, Gökhan Önder; Keskin, Seda; Department of Chemical and Biological Engineering; Graduate School of Sciences and Engineering; College of EngineeringIn this study, we used a high-throughput computational screening approach to examine the potential of metal-organic frameworks (MOFs) for capturing propane (C3H8) from different gas mixtures. We focused on Quantum MOF (QMOF) database composed of both synthesized and hypothetical MOFs and performed Grand Canonical Monte Carlo (GCMC) simulations to compute C3H8/N2/O2/Ar and C3H8/C2H6/CH4 mixture adsorption properties of MOFs. The separation of C3H8 from air mixture and the simultaneous separation of C3H8 and C2H6 from CH4 were studied for six different adsorption-based processes at various temperatures and pressures, including vacuum-swing adsorption (VSA), pressure-swing adsorption (PSA), vacuum-temperature swing adsorption (VTSA), and pressure-temperature swing adsorption (PTSA). The results of molecular simulations were used to evaluate the MOF adsorbents and the type of separation processes based on selectivity, working capacity, adsorbent performance score, and regenerability. Our results showed that VTSA is the most effective process since many MOFs offer high regenerability (>90%) combined with high C3H8 selectivity (>7 x 103) and high C2H6 + C3H8 selectivity (>100) for C3H8 capture from air and natural gas mixtures, respectively. Analysis of the top MOFs revealed that materials with narrow pores (<10 angstrom) and low porosities (<0.7), having aromatic ring linkers, alumina or zinc metal nodes, typically exhibit a superior C3H8 separation performance. The top MOFs were shown to outperform commercial zeolite, MFI for C3H8 capture from air, and several well-known MOFs for C3H8 capture from natural gas stream. These results will direct the experimental efforts to the most efficient C3H8 capture processes by providing key molecular insights into selecting the most useful adsorbents.Publication Metadata only Atomically dispersed zeolite-supported rhodium complex: selective and stable catalyst for acetylene semi-hydrogenation(Academic Press Inc., 2024) Su Yordanli, Melisa; Hoffman, Adam S.; Hong, Jiyun; Perez-Aguilar, Jorge E.; Saltuk, Aylin; Akgül, Deniz; Demircan, Oktay; Ateşin, Tülay A.; Aviyente, Viktorya; Gates, Bruce C.; Bare, Simon R.; Department of Chemical and Biological Engineering; Zhao, Yuxin; Bozkurt, Özge Deniz; Öztulum, Samira Fatma Kurtoğlu; Uzun, Alper; Department of Chemical and Biological Engineering; Koç University Tüpraş Energy Center (KUTEM) / Koç Üniversitesi Tüpraş Enerji Merkezi (KÜTEM); Koç University Surface Science and Technology Center (KUYTAM) / Koç Üniversitesi Yüzey Teknolojileri Araştırmaları Merkezi (KUYTAM); Graduate School of Sciences and Engineering; College of EngineeringSupported rhodium catalysts are known to be unselective for semi-hydrogenation reactions. Here, by tuning the electronic structure of supported mononuclear rhodium sites determined by the metal nuclearity and the electron-donor properties of the support, we report that atomically dispersed HY zeolite-supported rhodium with reactive acetylene ligands affords a stable ethylene selectivity > 90 % for acetylene semi-hydrogenation at 373 K and atmospheric pressure, even when ethylene is present in a large excess over acetylene. Infrared and X-ray absorption spectra and measurements of rates of the catalytic reaction complemented with calculations at the level of density functional theory show how the catalyst performance depends on the electronic structure of the rhodium, influenced by the support as a ligand that is a weak electron donor.