Kaya, Murat
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Kaya,Murat Murat, Kaya M., Kaya Kaya M. Kaya, Murat K.,Murat K., Murat M.,Kaya Kaya,M. Murat Kaya
Job Title
Profesör Doktor
Email Address
muratkaya@atilim.edu.tr
Main Affiliation
Chemical Engineering
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WoS Researcher ID
Research Topics
Domains
Physical Sciences
Fields
Materials ScienceChemical EngineeringChemistry
Subfields
Materials ChemistryCatalysisOrganic ChemistryProcess Chemistry and TechnologyElectronic, Optical and Magnetic Materials
Specific Research Areas
Hydrogen Storage and Materials
Ammonia Synthesis and Nitrogen Reduction
Nanomaterials for catalytic reactions
Carbon dioxide utilization in catalysis
Gold and Silver Nanoparticles Synthesis and Applications
Sustainable Development Goals
1NO POVERTY
0
Research Products
2ZERO HUNGER
0
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3GOOD HEALTH AND WELL-BEING
3
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4QUALITY EDUCATION
0
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5GENDER EQUALITY
0
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6CLEAN WATER AND SANITATION
9
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7AFFORDABLE AND CLEAN ENERGY
25
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8DECENT WORK AND ECONOMIC GROWTH
0
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9INDUSTRY, INNOVATION AND INFRASTRUCTURE
4
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10REDUCED INEQUALITIES
0
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11SUSTAINABLE CITIES AND COMMUNITIES
1
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12RESPONSIBLE CONSUMPTION AND PRODUCTION
0
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13CLIMATE ACTION
0
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14LIFE BELOW WATER
4
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15LIFE ON LAND
0
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16PEACE, JUSTICE AND STRONG INSTITUTIONS
0
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17PARTNERSHIPS FOR THE GOALS
0
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Documents
43
Citations
2181
h-index
23

This researcher does not have a WoS ID.
Publication Collaboration
| Affiliation Name | Count |
|---|---|
| Atilim University | 39 |
| Van Yüzüncü Yıl Üniversitesi | 24 |
| Middle East Technical University | 13 |
| Dicle University | 2 |
| Northeastern University | 1 |
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Data obtained from OpenAlex

Scholarly Output
59
Articles
38
Views / Downloads
123/249
Supervised MSc Theses
17
Supervised PhD Theses
2
WoS Citation Count
2012
Scopus Citation Count
1983
Patents
0
Projects
6
WoS Citations per Publication
34.10
Scopus Citations per Publication
33.61
Open Access Source
3
Supervised Theses
19
| Journal | Count |
|---|---|
| Applied Catalysis B: Environmental | 9 |
| ChemistrySelect | 4 |
| New Journal of Chemistry | 3 |
| Analytical Chemistry | 1 |
| Chemical Communications | 1 |
Current Page: 1 / 6
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59 results
Scholarly Output Search Results
Now showing 1 - 10 of 59
Article Citation - WoS: 28Citation - Scopus: 30Functionalized Polysulfide Copolymers With 4-Vinylpyridine Via Inverse Vulcanization(Elsevier Science Bv, 2019-06) Berk, Hasan; Balci, Burcu; Ertan, Salih; Kaya, Murat; Cihaner, AtillaA new series of functional polysulfide copolymers called poly(sulfur-random-4-vinylpyridine) (poly(S-r-4VP)) was synthesized via inverse vulcanization technique by ring opening polymerization of elemental sulfur in the presence of 4-vinylpyridine (4VP). The corresponding copolymers can be post functionalized by using amine group in 4VP unit to get polymers bearing various properties. Elemental sulfur was heated up to 160 degrees C and 4VP was added slowly to a clear yellowish orange colored liquid at this temperature. The reaction mixture was vitrified to form a reddish-brown polymeric material at 180 degrees C in 1 h. The products were characterized by using FTIR, NMR, and Raman spectroscopic techniques. Poly(S-r-4VP) copolymers are soluble in common solvents like dichloromethane, chloroform and tetrahydrofuran. Weight-average molecular weights of poly(S-r-4VP) copolymers with different wt% 4VP were measured by using gel permeation chromatography technique. The polysulfide copolymers with different wt% 4VP have high weight-average molecular weights with polydispersity indeces (PDI) in a range from 1.88 to 4.06 measured by gel permeation chromatography. Post functionalization of the copolymer with 50 wt% 4VP as an example was performed successfully by using alkyl bromide to get N-alkyl quaternized 4VP in polymer backbone.Master Thesis Amin Boranın Dehidrojenlenmesi için Bakır Nanoparçacık Eklenmiş Politiyofenin Hazırlanması(2017) Alablaq, Salha; Kaya, MuratNanokatalizörler sahip oldukları büyük yüzey-hacim oranları sebebi ile yüksek katalitik aktivite gösteren malzemeler olarak bilinmektedirler. Koloidal nanoparçacıkların sulu çözeltileri gibi homojen nanokatalizörler ise reaksiyonun oluşması için kullanılan başlangıç maddeleri ve oluşan ürünler ile aynı fazda bulunmaktadır. Bu tip katalizörlerin heterojen katalizörlere karşı başlıca avantajı sahip oldukları yüksek seçicilik olarak sayılabilir. Ancak düşük termal kararlılıkları, ciddi metal kirliliği ve reaksiyon ortamından geri kazanımındaki zorluk homojen katalizörlerin karşılaştığı başlıca zorluklardır. Bu zorlukların üstesinden gelebilmek için heterojen nanokatalizörler yaygın olarak kullanılmaktadır. Bu tür katalizörlerde metal nanoparçacıklar silika, alumiyum ve karbon temelli malzemelerin üzerine sabitlenmektedir. Günümüzde ise bazı polimer destek malzemeleri kolay ve ucuz üretim metodları sebebi ile büyük ilgi toplamaktadır. Hidrojen en önemli temiz enerji kaynaklarından biri olarak bilinmektedir. Bu sebeple metal hidrürler, kimyasal hidrürler, organik moleküller, metal organik kafesler ve karbon nanotüpler gibi hidrojen depolama malazemelerinin üretimi için birçok çalışma yapılmaktadır. Bu hidrojen depolama malzemleri arasında kimyasal hidrürler yüksek hidrojen depolama kapasitesine sahip olmaları sebebi ile büyük ilgi görmektedir. Kimyasal hidrürler arasından amin boran, yüksek hidrojen depolama kapasitesi (kütlece 19.6 %), yüksek kararlılık ve düşük toksisiteye sahip olması sebebi ile büyük önem kazanmıştır. Uygun katalizör kullanımı ile ılımlı şartlarda 1 mol amin borandan 3 mol hidrojen eldesi mümkündür. Amin borandan hidrojen eldesinde kinetik parametrelerin iyileştirilmesi için yüksek etkiye sahip katalizörlerin geliştirilmesi, hidrojen enerjisinin uygulamaları için çok önemlidir. Bu tezde, amin borandan sulu ortamda hidrojen eldesi için politiyofen üzerine bakır nanoparçacıkların eklendiği katalizörün hazırlanması için uygun bir yöntem sunulmaktadır. Bunun için ilk olarak politiyofen destek malzemesi hazırlanmıştır. Daha sonra bakır iyonları ıslak emdirme yöntemi ile polimer destek malzemesinin üzerine eklenmiştir. Bu aşamadan sonra bakır iyonları sodium borohidrür kullanılarak indirgenmiş ve bakır nanoparçacıklar elde edilmiştir. Daha sonra hazırlanan katalizörün katalitik aktivitesi ortaya çıkarılmıştır. İlk çevrim frekansı 11.8 dk-1 olarak bulunmuştur. Buna ek olarak, hazırlanan katalizörün kararlılığı ve tekrar kullanılabilme kapasitesi bulunmuştur. Hazırlanan katalizör oldukça iyi kararlılık ve tekrar kullanılabilme kapasitesine sahiptir. Bakır eklenmiş politiyofen katalizörü amin boranın hidrolitik olarak dehidrojenlenmesindeki beşinci tekrar kullanımından sonra benzer aktivite göstermiştir.Article Citation - WoS: 51Citation - Scopus: 54Atomic Layer Deposition-sio<sub>2</Sub> Layers Protected Pdconi Nanoparticles Supported on Tio<sub>2</Sub> Nanopowders: Exceptionally Stable Nanocatalyst for the Dehydrogenation of Formic Acid(Elsevier Science Bv, 2017-08) Caner, Nurdan; Bulut, Ahmet; Yurderi, Mehmet; Ertas, Ilknur Efecan; Kivrak, Hilal; Kaya, Murat; Zahmakiran, MehmetTiO2 nanopowders supported trimetallic PdCoNi alloy nanoparticles were simply and reproducibly prepared by wet-impregnation followed by simultaneous reduction method, then to enhance their stability against to sintering and leaching atomic layer deposition (ALD) technique was utilized to grow SiO2 layers amongst these surface bound PdCoNi alloy nanoparticles (PdCoNi/TiO2-ALD-SiO2). These new nanomaterials are characterized by the combination of complimentary techniques and sum of their results exhibited that the formation of ALD-SiO2 layers protected well-dispersed and highly crystalline PdCoNi alloy nanoparticles (ca. 3.52 nm) supported on TiO2 nanopowders. The catalytic performance of the resulting PdCoNi/TiO2-ALD-SiO2 in terms of activity, selectivity and stability was investigated in the dehydrogenation of aqueous formic acid (HCOOH), which has recently been suggested as a promising hydrogen storage material with a 4.4 wt% hydrogen capacity, solution under mild conditions. The results collected from our systematic studies revealed that PdCoNi/TiO2-ALD-SiO2 nanomaterial can act as highly active and selective nanocatalyst in the formic acid dehydrogenation at room temperature by providing an initial turnover frequency (TOF) value of 207 mol H-2/mol metal;: h and >99% of dehydrogenation selectivity at almost complete conversion. More importantly, the catalytic reusability experiments separately carried out with PdCoNi/TiO2-ALD-SiO2 and PdCoNi/TiO2 nanocatalysts in the dehydrogenation of formic acid under more forcing conditions pointed out that PdCoNi/TiO2-ALD-SiO2 nanocatalyst displays unprecedented catalytic stability against to leaching and sintering throughout the reusability experiments it retains almost its inherent activity, selectivity and conversion even at 20th reuse, whereas analogous PdCoNi/TiO2 completely lost its catalytic performance. (C) 2017 Elsevier B.V. All rights reserved.Article Citation - WoS: 137Citation - Scopus: 150Palladium(0) Nanoparticles Supported on Silica-Coated Cobalt Ferrite: a Highly Active, Magnetically Isolable and Reusable Catalyst for Hydrolytic Dehydrogenation of Ammonia Borane(Elsevier, 2014-04) Akbayrak, Serdar; Kaya, Murat; Volkan, Murvet; Ozkar, SaimPalladium(0) nanoparticles supported on silica-coated cobalt ferrite (Pd(0)/SiO2-CoFe2O4) were in situ generated during the hydrolysis of ammonia borane, isolated from the reaction solution by using a permanent magnet and characterized by ICP-OES, XRD, TEM, TEM-EDX, XPS and the N-2 adsorption-desorption techniques. All the results reveal that well dispersed palladium(0) nanoparticles were successfully supported on silica coated cobalt ferrite and the resulting Pd(0)/SiO2-CoFe2O4 are highly active, magnetically isolable, and recyclable catalysts in hydrogen generation from the hydrolysis of ammonia borane with an unprecedented turnover frequency (TOF, calculated on the basis of the total amount of Pd) of 254 mol H-2 (mol Pd min)(-1) at 25 +/- 0.1 degrees C. The reusability tests reveal that Pd(0)/SiO2-CoFe2O4 are still active in the subsequent runs of hydrolysis of ammonia borane providing 100% conversion. Pd(0)/SiO2-CoFe2O4 provide the highest catalytic activity with a TOF value of 198 mol H-2 (mol Pd min)(-1) in the 10th use in hydrogen generation from the hydrolysis of ammonia borane as compared to the other palladium catalysts. The work reported here also includes the kinetic studies depending on the temperature to determine the activation energy of the reaction (E-a = 52 +/- 2 kJ/mol) and the effect of catalyst concentration on the rate of hydrolytic dehydrogenation of ammonia borane, respectively. (C) 2013 Elsevier B.V. All rights reserved.Article Citation - WoS: 9Citation - Scopus: 10Chromium Based Metal-Organic Framework Mil-101 Decorated Palladium Nanoparticles for the Methanolysis of Ammonia-Borane(Royal Soc Chemistry, 2020) Caner, Nurdan; Yurderi, Mehmet; Bulut, Ahmet; Kanberoglu, Gulsah Saydan; Kaya, Murat; Zahmakiran, MehmetPalladium nanoparticles stabilized by an MIL-101 metal-organic framework (Pd@MIL-101) are synthesized by a novel synthesis approach. A Pd@MIL-101 catalyst facilitates H(2)generation from the methanolysis of ammonia-borane with record catalytic activity (TOF = 1080 min(-1)) at room temperature. Moreover, the exceptional stability of Pd@MIL-101 makes it a reusable heterogeneous catalyst in this catalytic transformation.Correction Citation - WoS: 1Citation - Scopus: 2Supported Copper-Copper Oxide Nanoparticles as Active, Stable and Low-Cost Catalyst in the Methanolysis of Ammonia-Borane for Chemical Hydrogen Storage (vol 165, Pg 169, 2015)(Elsevier, 2016-06) Yurderi, Mehmet; Bulut, Ahmet; Ertas, Ilknur Efecan; Zahmakiran, Mehmet; Kaya, Murat[No Abstract Available]Article Polysulfur Copolymer as a Support Material for the Preparation of a Novel Multifunctional Photocatalytic Composite Material(Springer, 2025-04-06) Kesimal, Busra; Guner, Zuhal Vanli; Cihaner, Atilla; Kaya, Murat; Vanli Guner, ZuhalOne-step addition of magnetic nanoparticles and titanium dioxide nanoparticles into polysulfur copolymer as cheap and available support was reported for the first time to prepare the magnetically separable heterogeneous catalyst, PolyS-MNP-TiO2. The photocatalytic activities of the PolyS-MNP-TiO2 composite material and its constituents were examined in the methylene blue (MB) degradation, textile-based wastewater simulant, exposed to solar light. Detailed characterization of the catalysts was performed with SEM, TEM, and EDX measurements. The photocatalytic activity of the resulting composite was figured out in the removal of methylene blue dye by using a solar simulator. Significantly, the as-prepared PolyS-MNP-TiO2 exhibits exceptional photocatalytic activity and total degradation of dye molecules was achieved in 60 min. Additionally, the prepared novel photocatalyst showed enhanced stability and reusability due to the magnetic behavior of the composite material and the same portion of catalyst was used in five successive tries without apparent loss in catalytic activity by eliminating long and work-loaded processes like filtration and centrifugation.Article Citation - WoS: 81Citation - Scopus: 89New Approach for the Surface Enhanced Resonance Raman Scattering (serrs) Detection of Dopamine at Picomolar (pm) Levels in the Presence of Ascorbic Acid(Amer Chemical Soc, 2012-08-30) Kayat, Murat; Volkan, Murvet; Kaya, MuratThe development of a novel surface-enhanced resonance Raman scattering (SERRS) platform that allows fast and sensitive detection of dopamine (DA) has been reported. The iron-nitrilotriacetic acid attached silver nanoparticle (Ag-Fe(NTA)) substrate provides remarkable sensitivity and reliable repeatability. The advantages of both the surface functionalization for specific analytes and the SERRS are integrated into a single functional unit. While the silver core gives the necessary enhancing properties, the Fe-NTA receptors can trap DA adjacent the silver core and the NTA-Fe-DA complex formed provides resonance enhancement with a 632.8 nm laser. DA could be detected in pM level without any pretreatment with a reliable discrimination against AA, by utilizing low laser power (10 mW) and short data acquisition time (10 s). The high sensitivity along with the improved selectivity of this sensing approach is a significant step toward molecular diagnosis of Parkinson's disease.Article Citation - WoS: 143Citation - Scopus: 149Carbon Dispersed Copper-Cobalt Alloy Nanoparticles: a Cost-Effective Heterogeneous Catalyst With Exceptional Performance in the Hydrolytic Dehydrogenation of Ammonia-Borane(Elsevier, 2016-01) Bulut, Ahmet; Yurderi, Mehmet; Ertas, Ilknur Efecan; Celebi, Metin; Kaya, Murat; Zahmakiran, MehmetHerein, we report the development of a new and cost-effective nanocatalyst for the hydrolytic dehydrogenation of ammonia-borane (NH3BH3), which is considered to be one of the most promising solid hydrogen carriers due to its high gravimetric hydrogen storage capacity (19.6 wt%) and low molecular weight. The new catalyst system consisting of bimetallic copper-cobalt alloy nanoparticles supported on activated carbon was simply and reproducibly prepared by surfactant-free deposition-reduction technique at room temperature. The characterization of this new catalytic material was done by the combination of multi-pronged techniques including ICP-MS, XRD, XPS, BFTEM, HR-TEM, STEM and HAADF-STEM-line analysis. The sum of their results revealed that the formation of copper-cobalt alloy nanoparticles (d(mean) =1.8 nm) on the surface of activated carbon (CuCo/C). These new carbon supported copper-cobalt alloy nanoparticles act as highly active catalyst in the hydrolytic dehydrogenation of ammonia-borane, providing an initial turnover frequency of TOF = 2700 h(-1) at 298 K, which is not only higher than all the non-noble metal catalysts but also higher than the majority of the noble metal based homogeneous and heterogeneous catalysts employed in the same reaction. More importantly, easy recovery and high durability of these supported CuCo nanoparticles make CuCo/C recyclable heterogeneous catalyst for the hydrolytic dehydrogenation of ammonia-borane. They retain almost their inherent activity even at 10th catalytic reuse in the hydrolytic dehydrogenation of ammonia-borane at 298K. (C) 2015 Elsevier B.V. All rights reserved.Doctoral Thesis Yakın Kızılötesi Bölgede Yüksek Işık-ısı Çevrimine Sahip Özgün Nanoyapıların Hazırlanması ve Fototermal Etkinliklerinin Araştırılması(2023) Güner, Zuhal Selvi Vanlı; Kaya, MuratNano boyutlu malzemelerin geniş yüzey alanı-hacim oranı, geçmişten bugüne kadar keşfedilen beklenmedik mekanik, elektriksel ve optik özellikler sayesinde yeni ve heyecan verici araştırma alanlarının ortaya çıkmasını sağlamıştır. Bu özellikler sayesinde nano-yapılar moleküler görüntüleme, erken hastalık teşhisi, doku mühendisliği, atık su arıtma, gıda paketleme, UV koruması, endüstriyel katalizörler, elektronik, piller ve kuantum bilgisayarlar alanlarında geniş bir uygulama alanı sunmaktadır. Hem altın nanoparçacıkların hem de manyetik nanoparçacıkların, ışık ısı çevrimi son zamanlarda deneysel ve teorik olarak incelenmektedir. Ancak daha önce de belirtildiği gibi bu dönüşüm özelliği her nanomalzemenin yapısına ve bileşimine bağlı olarak farklılık göstermektedir. Farklı nanoparçacık yapılarının dekore ve organize edilmesi ile nanoparçacıkların plazmonik özellikleri geliştirilerek ışıktan ısıya yüksek dönüşüm elde edilmesi mümkün gözükmektedir. Bu bilgiler ışığında, benzerlerinden farklı optik özellikleri nedeniyle yüksek ışık-ısı dönüşümüne sahip nanoyapıların hazırlanması amaçlanmıştır. Bu amaçla içi boş altın nanoparçacıklar ve silika kaplı manyetik demir oksit nanoparçacıklar üzerinde çalışılmıştır. Bu amaçla, içi boş altın nanoparçacıklar ve silika kaplı manyetik demir vi oksit nanoparçacıklar hazırlanmış ve daha sonra küçük boyutlu altın nanoparçacıklar ve gümüş-altın bimetalik nanoparçacıklar ile bezenmiştir. Bu çalışmada dört farklı nanoyapı hazırlanmış ve bunların ışığı ısıya dönüştürme kapasitesi araştırılmıştır. Bu yapılardan ilk ikisi, 24 nm boyutunda ve 5-10 nm kalınlığında kabuğa sahip içi boş altın nanoparçacıklar (HAuNPs) üzerine 1-3 nm boyutunda altın (AuNPs) ve gümüş-altın bimetalik nanoparçacıkların (AgAuNPs) eklenmesiyle hazırlanmıştır. (HAuNPs-AuNPs, HAuNPs-AgAuNPs). Üçüncü ve dördüncü parçacık yapıları, sırasıyla silika kabuk ile kaplanmış manyetik demir oksit nanoparçacıkların üzerine 1-3 nm boyutunda hem altın nanoparçacıklar ve altın-gümüş bimetalik nanoparçaçıklar eklenerek hazırlanmıştır(Fe3O4-SiO2-AuNPs, Fe3O4-SiO2-AgAuNPs). Hazırlanan yapıların karakterizasyonu, yüksek çözünürlüklü transmisyon elektron mikroskobu (HR-TEM), enerji dağılımlı X-ışını spektroskopisi (EDX), ultraviyole ve görünür spektroskopi (UV-Vis) ve titreşimli numune manyetometresi (VSM), ve hazırlanan yapıların fototermal etkileri, çözelti içinde, 808 nm dalga boyunda ışık kaynağı kullanılarak araştırılmıştır.
