Abstract
Both metal and nonmetal electrodes normally exhibit a low CO partial current density (JCO) of lower than 15 mA cm−2 during CO2 electrochemical reduction to CO in the aqueous phase, which is primarily attributed to the low solubility and mass transfer rate of CO2. Modifying the catalyst surface with a hydrophobic substance is recognized as an effective strategy for addressing this challenge. However, the formation of a hydrophobic layer may evacuate the electrode surface from electrolyte. In this study, a one-step electrodeposition method was employed to prepare a polytetrafluoroethylene (PTFE)-doped Zn@ZnAg porous catalyst, and two doping approaches were investigated, which involved surface-layer doping and bulk-phase doping. Energy-dispersive spectrometer (EDS) mapping and X-ray diffractometer (XRD) analyses revealed that bulk-phase doping enabled uniform dispersion of PTFE over the pore walls of the ZnAg alloy. The results showed the Janus catalyst with a PTFE-doped side and an undoped one, achieved a remarkable JCO of 34.19 mA cm−2 with a CO Faradaic efficiency (FECO) of 90.75 % in 0.1 M KHCO3 electrolyte at a potential of −2.6 V vs. SCE.
Original language | English |
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Article number | 131799 |
Journal | Separation and Purification Technology |
Volume | 362 |
DOIs | |
State | Published - 30 Jul 2025 |
Bibliographical note
Publisher Copyright:© 2025 Elsevier B.V.
Keywords
- CO electroreduction
- Janus electrode
- Reaction environment
- ZnAg alloy catalyst
ASJC Scopus subject areas
- Analytical Chemistry
- Filtration and Separation