Reactive CO2 capture electrolysis at low voltage and high single-pass conversion enabled by ultra-low loading molecular catalyst

We demonstrate a high-efficiency reactive CO 2 capture electrolysis system, utilizing ultra-low loading CoPc/CNT catalysts. By achieving 55.1% single-pass conversion and reducing voltage by 30%, this integrated approach offers a low-cost, energy-saving pathway for sustainable carbon utilization. Integrating electrochemical CO 2 conversion with carbon capture extends the CO 2 source beyond pure or point-source streams. By directly interfacing with capture units, reactive CO 2 capture electrolysis circumvents the energy-intensive regeneration and compression processes to supply pure CO 2 stream, also minimizes the amount of unreacted CO 2 through gas-fed CO 2 electrolysis. However, the conversion pathway is hampered by high electrolyser voltages and reliance on precious and thick metal catalysts (> 2.0 mg cm −2 ). Here, we report an energy-efficient reactive CO 2 capture electrolysis system enabled by an ultra-low loading molecular catalyst (cobalt phthalocyanine anchored onto multi-walled carbon nanotubes, CoPc/CNT). When the CoPc/CNT exceeds 0.2 mg cm −2 loading on cathode, the thicker CoPc/CNT layer largely increase electrical and mass transfer resistances. This limits the availability of local CO 2 at the catalyst surface, suppressing the formation of adsorbed intermediates (COOH*/CO*) on cobalt centres, as observed by operando Raman spectroscopy. Benefiting from the features, the electrolysis system achieves a single-pass CO 2 conversion of 55.1% at 300 mA cm −2 and a faradaic efficiency of CO (FE CO ) 84.7% at a 0.2 mg cm −2 . At 100 mA cm −2 , the synergistic combination of CoPc/CNT with a two-layer membrane architecture reduces electrolyser voltage by 30% to widely used bipolar membrane (BPM)-incorporated electrolyser and 17% voltage to metal catalyst-based cathode. This study offers a cost-effective molecular catalyst for reactive CO 2 capture electrolysis and paves the way for energy-efficient carbon capture and utilisation integrated systems.

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Publication Details

Journal
Journal of Energy Chemistry
Published
2026-03-13
DOI
https://doi.org/10.1016/j.jechem.2026.03.008
Primary Topic
CO2 Reduction Techniques and Catalysts
Type
article
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article

Reactive CO2 capture electrolysis at low voltage and high single-pass conversion enabled by ultra-low loading molecular catalyst

Mengxin Liu, Yasuhiro Sakamoto, Catherine Stampfl, George Li et al.
Journal of Energy Chemistry
CO2 Reduction Techniques and Catalysts
article

Reactive CO2 capture electrolysis at low voltage and high single-pass conversion enabled by ultra-low loading molecular catalyst

Mengxin Liu, Yasuhiro Sakamoto, Catherine Stampfl, George Li, Yijiao Jiang, Yuming Wu, Lizhuo Wang, Zhiqiang Zhao, David Inglis, Feng Jiao
article en

Abstract

We demonstrate a high-efficiency reactive CO 2 capture electrolysis system, utilizing ultra-low loading CoPc/CNT catalysts. By achieving 55.1% single-pass conversion and reducing voltage by 30%, this integrated approach offers a low-cost, energy-saving pathway for sustainable carbon utilization. Integrating electrochemical CO 2 conversion with carbon capture extends the CO 2 source beyond pure or point-source streams. By directly interfacing with capture units, reactive CO 2 capture electrolysis circumvents the energy-intensive regeneration and compression processes to supply pure CO 2 stream, also minimizes the amount of unreacted CO 2 through gas-fed CO 2 electrolysis. However, the conversion pathway is hampered by high electrolyser voltages and reliance on precious and thick metal catalysts (> 2.0 mg cm −2 ). Here, we report an energy-efficient reactive CO 2 capture electrolysis system enabled by an ultra-low loading molecular catalyst (cobalt phthalocyanine anchored onto multi-walled carbon nanotubes, CoPc/CNT). When the CoPc/CNT exceeds 0.2 mg cm −2 loading on cathode, the thicker CoPc/CNT layer largely increase electrical and mass transfer resistances. This limits the availability of local CO 2 at the catalyst surface, suppressing the formation of adsorbed intermediates (COOH*/CO*) on cobalt centres, as observed by operando Raman spectroscopy. Benefiting from the features, the electrolysis system achieves a single-pass CO 2 conversion of 55.1% at 300 mA cm −2 and a faradaic efficiency of CO (FE CO ) 84.7% at a 0.2 mg cm −2 . At 100 mA cm −2 , the synergistic combination of CoPc/CNT with a two-layer membrane architecture reduces electrolyser voltage by 30% to widely used bipolar membrane (BPM)-incorporated electrolyser and 17% voltage to metal catalyst-based cathode. This study offers a cost-effective molecular catalyst for reactive CO 2 capture electrolysis and paves the way for energy-efficient carbon capture and utilisation integrated systems.

Journal of Energy ChemistryVol. 117
The University of Sydney (AU), Washington University in St. Louis (US), Macquarie University (AU)
Responsible consumption and production
Openalex Percentile: Top 27%
CO2 Reduction Techniques and Catalysts
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