Characterization of Zeolitic Imidazolate Framework–derived Polyhedral Carbonaceous Material and its Application to Electrocatalyst for Oxygen Reduction Reaction

A porous carbonaceous material is synthesized by direct carbonization of zeolitic imidazolate framework-67 (ZIF-67). A series of analytical tools such as scanning/transmission electron microscopy, gas chromatography/mass spectroscopy, thermogravimetric analysis, nitrogen adsorption, X-ray diffractio...

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Veröffentlicht in:International journal of electrochemical science 2016-11, Vol.11 (11), p.9295-9306
Hauptverfasser: Park, Kyo Sung, Jin, Seon-ah, Lee, Kang Hee, Lee, Junho, Song, Inyong, Lee, Byoung-Sun, Kim, Sookyung, Sohn, Jeongsoo, Pak, Chanho, Kim, Gunha, Doo, Seok-Gwang, Kwon, Kyungjung
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Sprache:eng
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Zusammenfassung:A porous carbonaceous material is synthesized by direct carbonization of zeolitic imidazolate framework-67 (ZIF-67). A series of analytical tools such as scanning/transmission electron microscopy, gas chromatography/mass spectroscopy, thermogravimetric analysis, nitrogen adsorption, X-ray diffraction, X-ray photoelectron spectroscopy and 3D tomography are conducted for the characterization of the prepared carbonaceous material (ZIF-C). ZIF-C has a well-defined concave dodecahedral shape, and its chemical composition, surface area and electrical conductivity substantially depend on carbonization temperature. ZIF-C heat-treated at 800°C (ZIF-C-800) shows a typical nitrogen adsorption-desorption isotherm of mesoporous materials with unimodal pores around 2 nm and sufficiently high electrical conductivity comparable to that of carbon nanotubes. ZIF-C-800 has Co metal particles wrapped by graphene layers on the walls of the interior open channels, and its framework is composed of Co-N, C-N species and C-C networks. ZIF-C-800 also displays the highest oxygen reduction reaction catalytic activity among ZIF-C treated at various temperatures, and its feasibility as cathode electrocatalysts for fuel cells is demonstrated by confirming the single cell performance.
ISSN:1452-3981
1452-3981
DOI:10.20964/2016.11.27