journal article·2019-06-12

Selective Alcohol Electrooxidation by ZIF-8 Functionalized Pt/Carbon Catalyst

Claudia Eßbach, Irena Senkovska, Tobias Unmüssig, Anna Fischer, Stefan Kaskel

ACS Applied Materials & Interfaces· Volume 11· Issue 23
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Abstract

Highly selective electrooxidation catalysts were synthesized by functionalizing a commercially available reference electrooxidation catalyst (Pt/Vulcan XC 72R) with a coating of the highly hydrophobic porous zeolitic imidazolate framework ZIF-8, an adsorbent with high affinity for the extraction of aliphatic alcohols from water. According to cyclovoltammetric studies in alkaline media at 25 °C, the ZIF-8 functionalized catalyst shows a high selectivity for the electrooxidation of small alcohols such as ethanol and methanol over more hydrophobic alcohols ( n-butanol, n-propanol). In contrast, the noncoated reference catalyst (Pt/Vulcan XC 72R) oxidizes all investigated alcohols with comparable current densities. Tafel curves confirm these observations and indicate a limited conversion of long chain alcohols, especially n-butanol, caused by the high affinity of the ZIF-8 for this molecule resulting in significant diffusion limitations.
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Research context

OpenAlex topics: Metal-Organic Frameworks: Synthesis and Applications · Fuel Cells and Related Materials · Electrochemical Analysis and Applications

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

Technische Universität Dresden, Bergstraße 66, 01062 Dresden, Germany

Institut für Anorganische und Analytische Chemie, Fakultät für Chemie und Pharmazie, Albert-Ludwigs-Universität Freiburg, Albertstraße 21, 79104 Freiburg, Germany

Freiburg Material Research Center, Albert-Ludwigs-Universität Freiburg, Stefan-Meier-Straße 21, 79104 Freiburg, Germany

Freiburg Center for Interactive Materials and Bioinspired Technologies, Albert-Ludwigs-Universität Freiburg, Georges-Köhler-Allee 105, 79110 Freiburg, Germany

Funding

Bundesministerium f?r Bildung und Forschung · Deutsche Forschungsgemeinschaft

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