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Covalent Organic Framework (COF) derived Ni-N-C Catalysts for Electrochemical CO2 Reduction: Unraveling Fundamental Kinetic and Structural Parameters of the Active Sites

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Timoshenko,  Janis
Interface Science, Fritz Haber Institute, Max Planck Society;

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Jeon,  Hyosang
Interface Science, Fritz Haber Institute, Max Planck Society;

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Haase,  Felix
Interface Science, Fritz Haber Institute, Max Planck Society;

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Rettenmaier,  Clara
Interface Science, Fritz Haber Institute, Max Planck Society;

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Roldan Cuenya,  Beatriz
Interface Science, Fritz Haber Institute, Max Planck Society;

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Citation

Li, C., Ju, W., Vijay, S., Timoshenko, J., Mou, K., Cullen, D. A., et al. (2022). Covalent Organic Framework (COF) derived Ni-N-C Catalysts for Electrochemical CO2 Reduction: Unraveling Fundamental Kinetic and Structural Parameters of the Active Sites. Angewandte Chemie International Edition, 61(15): e202114707. doi:10.1002/anie.202114707.


Cite as: https://hdl.handle.net/21.11116/0000-0009-E478-F
Abstract
Electrochemical CO2 reduction is a potential approach to convert CO2 into valuable chemicals using electricity as feedstock. Abundant and affordable catalyst materials are needed to upscale this process in a sustainable manner. Nickel-nitrogen-doped carbon (Ni-N-C) is an efficient catalyst for CO2 electro-reduction to CO, and the single-site Ni-Nx motif is believed as the active site. However, critical metrics for its catalytic activity, such as active site density and intrinsic turnover frequency, so far lack systematic discussion. In this work, we prepared a set of covalent organic framework (COF)-derived Ni-N-C catalysts, for which the Ni-Nx content could be adjusted by the pyrolysis temperature. The combination of high-angle annular dark-field scanning transmission electron microscopy and extended X-ray absorption fine structure evidenced the presence of Ni single-sites, and quantitative X-ray photoemission addressed the relation between active site density and turnover frequency.