Effect of the Nanostructured Zn/Cu Electrocatalyst Morphology on the Electrochemical Reduction of CO2 to Value-Added Chemicals
Piriya Pinthong a, Phongsathon Klongklaew a, Piyasan Praserthdam a, Joongjai Panpranot a
a Center of Excellence on Catalysis and Catalytic Reaction Engineering, Department of Chemical Engineering, Faculty of Engineering, Chulalongkorn University, Bangkok 10330, Thailand
Materials for Sustainable Development Conference (MATSUS)
Proceedings of Materials for Sustainable Development Conference (MAT-SUS) (NFM22)
#Suschem- Materials and electrochemistry for sustainable fuels and chemicals
Barcelona, Spain, 2022 October 24th - 28th
Organizers: Marta Costa Figueiredo and Raffaella Buonsanti
Poster, Piriya Pinthong, 281
Publication date: 11th July 2022

Zn/Cu electrocatalysts were synthesized by the electrodeposition method with various bath compositions and deposition times. X-ray diffraction results confirmed the presence of (101) and (002) lattice structures for all the deposited Zn nanoparticles. However, a bulky (hexagonal) structure with particle size in the range of 1–10 μm was obtained from a high-Zn-concentration bath, whereas a fern-like dendritic structure was produced using a low Zn concentration. A larger particle size of Zn dendrites could also be obtained when Cu2+ ions were added to the high-Zn-concentration bath. The catalysts were tested in the electrochemical reduction of CO2 (CO2RR) using an H-cell type reactor under ambient conditions. Despite the different sizes/shapes, the CO2RR products obtained on the nanostructured Zn catalysts depended largely on their morphologies. All the dendritic structures led to high CO production rates, while the bulky Zn structure produced formate as the major product, with limited amounts of gaseous CO and H2. The highest CO/H2 production rate ratio of 4.7 and a stable CO production rate of 3.55 μmol/min were obtained over the dendritic structure of the Zn/Cu–Na200 catalyst at −1.6 V vs. Ag/AgCl during 4 h CO2RR. The dissolution and re-deposition of Zn nanoparticles occurred but did not affect the activity and selectivity in the CO2RR of the electrodeposited Zn catalysts. The present results show the possibilities to enhance the activity and to control the selectivity of CO2RR products on nanostructured Zn catalysts.

Financial support from the Rachadapisek Sompote Endowment Fund for the Postdoctoral Fellowship, Chulalongkorn University for P.P., the Research Team Promotional Grant from the National Research Council of Thailand (NRCT) for J.P., and the Malaysia-Thailand Joint Authority (MTJA) Research Cess Fund are gratefully acknowledged.

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