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Molecular electrocatalysis for oxygen reduction by cobalt porphyrins adsorbed at liquid/liquid interfaces
Scopus
Toplam 141 atıf DOI
Molecular electrocatalysis for oxygen reduction at a polarized water/1,2-dichloroethane (DCE) interface was studied, involving aqueous protons, ferrocene (Fc) in DCE and amphiphilic cobalt porphyrin catalysts adsorbed at the interface. The catalyst, (2,8,13,17-tetraethyl-3,7,12,18-tetramethyl-5-p- amino-phenylporphyrin) cobalt(II) (CoAP), functions like conventional cobalt porphyrins, activating O2 via coordination by the formation of a superoxide structure. Furthermore, due to the hydrophilic nature of the aminophenyl group, CoAP has a strong affinity for the water/DCE interface as evidenced by lipophilicity mapping calculations and surface tension measurements, facilitating the protonation of the CoAP-O2 complex and its reduction by ferrocene. The reaction is electrocatalytic as its rate depends on the applied Galvani potential difference between the two phases. © 2010 American Chemical Society.
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Catalytic Hydrogen Evolution by Molybdenum-Based Ternary Metal Sulfide Nanoparticles
Scopus
Havuzumuzda 31 atıf almış
The search for highly active earth-abundant elements and nonexpensive catalysts for hydrogen evolution reaction is a vital and demanding task to minimize energy consumption. Transition metals incorporated into molybdenum sulfides are promising candidates for hydrogen evolution because of their unique chemical and physical properties. Here, we first describe a general strategy for the synthesis of particle-shaped molybdenum-based ternary refractory metal sulfides (MMoSx; M = Fe, Co, Ni, and Mn) through a simple hot-injection method. The newly developed materials are affirmed as valuable alternatives to noble-metal platinum because of their simple fabrication, inexpensiveness, and impressive catalytic performance. We present highly efficient catalysts for hydrogen evolution at a polarized water/1,2-dichloroethane interface by using decamethylferrocene (DMFc). The kinetics of hydrogen evolution studies are monitored by two-phase reactions using UV-vis spectroscopy and also further proven by gas chromotography. These ternary refractory metal sulfide catalysts show high catalytic activities upon hydrogen evolution comparable to platinum. The rate of hydrogen evolution for the MMoSx catalysts changed in the order Ni > Co > Fe > Mn according to the types of first-row transition metals.
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Kurumlar (3)
École Polytechnique Fédérale de Lausanne
Lausanne, Switzerland
Karamanoğlu Mehmetbey Üniversitesi
Karaman, Turkey
Selçuk Üniversitesi
Selçuklu, Turkey