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Updated: May 29, 2026

Synthesis and Performance Characterizations of Transition Metal Single Atom Catalyst for Electrochemical CO2 Reduction
Published on: April 10, 2018
Membrane-separated electrodes enable high-rate low-energy electrochemical carbon capture
Kaige Sun1,2, Mike Tebyetekerwa1,2, Hongxia Zhang1,2
1ARC Centre of Excellence for Green Electrochemical Transformation of Carbon Dioxide, The University of Queensland, Brisbane, QLD 4072, Australia.
None:
Electrochemical carbon dioxide (CO2) capture using supercapacitive systems is a promising green technology but remains limited by low uptake rates and high energy requirement. Here, we present a membrane-integrated supercapacitor system that addresses these challenges by decoupling electrode environments with a cation exchange membrane. This configuration sustains high hydroxide concentration at the gas-facing negative electrode, generated through dynamic water dissociation within the electric double layer. The resulting localized alkaline interface enhances CO2 capture by driving its conversion into (bi)carbonate species via a pH-swing mechanism. The system achieves a CO2 uptake of up to 893 mmol/kg with a fast rate of 1281 mmol/kg/hour at -1.4 V under 20% CO2. Energy consumption as low as 32 kJ/mol is obtained at -0.8 V under 20% CO2 together with a long lifetime over 200 hours at -1.0 V, 10% CO2. These findings establish a robust platform for electrochemical CO2 capture and underscore the importance of localized chemical environments in supercapacitive swing adsorption.
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