4.5 Article

Catalytic hydrogenation performance of ZIF-8 carbide for electrochemical reduction of carbon dioxide

Journal

CHINESE JOURNAL OF CHEMICAL ENGINEERING
Volume 39, Issue -, Pages 144-153

Publisher

CHEMICAL INDUSTRY PRESS CO LTD
DOI: 10.1016/j.cjche.2021.05.032

Keywords

Carbon dioxide; Electrochemistry; Selective catalytic reduction; Electrochemical hydrogen pump; Nitrogen-doping carbonized ZIF-8

Funding

  1. National Natural Science Foundation of China [U1663223, 21776034]
  2. Science Fund for Creative Research Groups of the National Natural Science Foundation of China [22021005]
  3. National Key Research and Development Program of China [2016YFB0101203]
  4. Educational Department of Liaoning Province of China [LT2015007]
  5. Fundamental Research Funds for the Central Universities [DUT16TD19]
  6. Changjiang Scholar Program [T2012049]

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The nitrogen-doped carbonized ZIF-8 with hierarchically porous structure is proposed as a carrier of Sn catalyst to enhance electron transfer and CO2 adsorption capacity. The interaction between ZIF-8 and Sn improves the conductivity and electron transfer efficiency, leading to significantly higher catalytic activity for CO2 reduction reaction compared to commercial Sn and other Sn-based catalysts.
The conversion of CO2 electrocatalytic hydrogenation into energy-rich fuel is considered to be the most effective way to carbon recycle. Nitrogen-doping carbonized ZIF-8 is proposed as carrier of the earth-rich Sn catalyst to overcome the limit of electron transfer and CO2 adsorption capacity of Sn. Hierarchically porous structure of Sn doped carbonized ZIF-8 is controlled by hydrothermal and carbonization conditions, which induces much higher specific surface area than that of the commercial Sn nanoparticle (1003.174 vs. 7.410 m(2).g(-1)). The shift of nitrogen peaks in X-ray Photoelectron Spectroscopy spectra indicates interaction between ZIF-8 and Sn, which induces the shift of electron cloud from Sn to the chemical nitrogen to enhance conductivity and regulate electron transfer from catalyst to CO2. Lower mass transfer resistance and Warburg resistance are investigated through EIS, which significantly improves the catalytic activity for CO2 reduction reaction (CO2RR). Onset potential of the reaction is reduced from -0.74 V to less than -0.54 V vs. RHE. The total Faraday efficiency of HCOOH and CO reaches 68.9% at -1.14 V vs. RHE, which is much higher than that of the commercial Sn (45.0%) and some other Sn-based catalyst reported in the literature. (C) 2021 The Chemical Industry and Engineering Society of China, and Chemical Industry Press Co., Ltd. All rights reserved.

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