4 research outputs found
Utilisation of gelatin as nitrogen source for N-doped carbon nanotubes and its performance for the oxygen reduction reaction
Gelatin is utilised as a nitrogen source to synthesise nitrogen (N)-doped carbon nanotubes (CNTs). The N-doped CNT was prepared by mixing gelatin and CNT, followed by calcination at 500 °C and 800 °C under N2 atmosphere. X-ray diffraction analysis shows that the higher gelatin weight ratio results in a decrease of the crystallisation. X-ray photoelectron spectroscopy deconvolution analysis confirms that pyridinic-N and pyrrolic-N have appeared at the surface of the samples. The higher calcination temperature affects the surface properties of N-doped CNT which tend to shift the pyrrolic-N to the pyridinic-N. Cyclic voltammetry analysis reveals that the presences of pyridinic-N and graphitic-N configuration have higher oxygen reduction reaction (ORR) activity compared to the N-pyrrolic structure. © 2022 Vietnam Academy of Science & Technology
Oxygen Plasma Induced Hierarchically Structured Gold Electrocatalyst for Selective Reduction of Carbon Dioxide to Carbon Monoxide
Electrochemical
reduction of CO<sub>2</sub> into C1 products with
high energy density has attracted attention due to the demands for
renewable energy sources. Herein, we demonstrate a selective electrocatalytic
CO<sub>2</sub> reduction system where the cathode consists of hierarchically
structured Au islands catalysts. To be more specific, the Au islands
were prepared by oxygen plasma treatment on the Au foil to increase
the current density for the selective production of carbon monoxide
with over 95% of faradaic efficiency. Faradaic efficiency, production
rate, and the onset potential for CO<sub>2</sub> reduction were significantly
improved by the expanded surface area compared with a polycrystalline
Au electrode. Furthermore, the performance of CO<sub>2</sub> reduction
to CO was enhanced by adding ionic liquid (1-butyl-3-methylimidazolium
tetrafluoroborate) which has high CO<sub>2</sub>-capture ability and
catalytic activity. On the other hand, the rate-determining step of
the Au electrode for the CO production determined by Tafel plots was
found to be consistent with the initial one electron transfer step
to form the surface-adsorbed CO<sub>2</sub><sup>•–</sup> intermediates regardless of the application of hierarchically structured
catalyst and ionic liquid in the CO<sub>2</sub> reduction system