Effect of Modifying Carbon Materials with Metal Phthalocynines and Palladium on Their Catalytic Activity in ORR

Author:

Bulanova Andzhela VladimirovnaORCID,Shafigulin Roman Vladimirovich,Vinogradov Kirill YurievichORCID,Tokranova Elena Olegovna,Martynenko Evgenia AndreevnaORCID,Vostrikov Sergey Vladimirovich,Podlipnov Vladimir VladimirovichORCID

Abstract

Bimetallic catalysts based on multi-walled carbon nanotubes (MWCNT), graphene oxide (GO) and ultradispersed diamonds (UDD) supports for the process of electroreduction of oxygen from alkaline electrolyte were obtained using high-temperature synthesis. The materials were characterized by low-temperature nitrogen adsorption, Raman spectroscopy, scanning electron microscopy and X-ray structure analysis. The synthesized bimetallic catalysts contain meso- and micropores. Based on the study by Raman spectroscopy, it is shown that high-temperature synthesis of MWCNT with metal phthalocyanines leads to doping of this material with nitrogen and the appearance of significant defects in the structure. Carbon nanotube-based catalysts showed enhanced activity compared to other carbon materials. Moreover, bimetallic catalysts based on cobalt phthalocyanine and palladium (MWCNT_CoPc_Pd) are characterized by higher activity on all carbon supports compared to materials contain on copper and palladium. The specific current density in the diffusion region of the MWCNT_CoPc_Pd catalyst is comparable to a commercial platinum electrode (Pt(20%)/C) and equals to 2.65 mA/cm2. The area of the electrochemically active surface of all the obtained catalysts was calculated from the CV data in a nitrogen atmosphere. The MWCNT_CoPc_Pd catalyst is characterized by high corrosivity: after 2500 revolutions, the current density in the diffusion region decreases by 7%, and, also, an increase in the values of E1/2 and Eonset is observed.

Funder

Russian Foundation for Basic Research

Russian Federation Ministry of Science and Higher Education

Publisher

MDPI AG

Subject

Physical and Theoretical Chemistry,Catalysis,General Environmental Science

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