A Vanadium Redox Flow Process for Carbon Capture and Energy Storage

Climate change mitigation by decreasing worldwide CO2 emissions is an urgent and demanding challenge that requires innovative technical solutions. This work, inspired by vanadium redox flow batteries (VRFB), introduces an integrated electrochemical process for carbon capture and energy storage. It utilizes established vanadium and ferricyanide redox couples for pH modulation for CO2 desorption and absorbent regeneration. The developed process consumes electricity during the daytime─when renewable electricity is available─to desorb CO2 and charge the cell, and it can regenerate the absorbent for further CO2 absorption while releasing electricity to the grid during nighttime when solar power is unavailable. This research explores the process fundamentals and scalability potential, through an extensive study of the system’s thermodynamics, transport phenomena, kinetics, and bench-scale operations. Cyclic voltammetry (CV) was utilized to study the thermodynamics of the process, mapping the redox profiles to identify ideal potential windows for operation. The CV results indicated that an overpotential of approximately 0.3 V was required for driving redox reactions. Additionally, polarization studies were conducted to select the practical operating potential, identifying 0.5 V as optimal for the CO2 desorption cycle to provide sufficient polarity to overcome activation barriers in addition to the Nernstian potential. Mass transfer analysis balanced conductivity and desorption efficiency, with a 1:1 ratio identified as optimal for redox-active species and background electrolyte concentration. To further enhance the kinetics of the redox reactions, plasma treatment of electrode surfaces was implemented, resulting in a 43% decrease in charge transfer resistance, as measured by electrochemical impedance spectroscopy (EIS) analysis. Finally, a bench-scale operation of the system demonstrated an energy consumption of 54 kJ/mol CO2, which is competitive with other electrochemical carbon capture technologies. Besides its energy competitiveness, the process offers multiple additional advantages, including the elimination of precious metal electrodes, oxygen insensitivity in flue gas, scalability inspired by VRFB technology, and the unique ability to function as a battery during the absorbent regeneration process, enabling efficient day-night operation.

Authors

Institutions

Publication Details

Journal
ACS ES&T Engineering
Published
2025-01-29
DOI
https://doi.org/10.1021/acsestengg.4c00631
Citations
7
Primary Topic
Carbon Dioxide Capture Technologies
Type
article
Field-Weighted Citation Impact
4.99

Funders

Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

A Vanadium Redox Flow Process for Carbon Capture and Energy Storage

Abdelrahman Refaie, Mohsen Afshari, Mohammad Rahimi, Prince Aleta et al.
7 citations
ACS ES&T Engineering
Carbon Dioxide Capture Technologies
4.99
article

A Vanadium Redox Flow Process for Carbon Capture and Energy Storage

Abdelrahman Refaie, Mohsen Afshari, Mohammad Rahimi, Prince Aleta, Ahmad Hassan
article en
7 citations

Abstract

Climate change mitigation by decreasing worldwide CO2 emissions is an urgent and demanding challenge that requires innovative technical solutions. This work, inspired by vanadium redox flow batteries (VRFB), introduces an integrated electrochemical process for carbon capture and energy storage. It utilizes established vanadium and ferricyanide redox couples for pH modulation for CO2 desorption and absorbent regeneration. The developed process consumes electricity during the daytime─when renewable electricity is available─to desorb CO2 and charge the cell, and it can regenerate the absorbent for further CO2 absorption while releasing electricity to the grid during nighttime when solar power is unavailable. This research explores the process fundamentals and scalability potential, through an extensive study of the system’s thermodynamics, transport phenomena, kinetics, and bench-scale operations. Cyclic voltammetry (CV) was utilized to study the thermodynamics of the process, mapping the redox profiles to identify ideal potential windows for operation. The CV results indicated that an overpotential of approximately 0.3 V was required for driving redox reactions. Additionally, polarization studies were conducted to select the practical operating potential, identifying 0.5 V as optimal for the CO2 desorption cycle to provide sufficient polarity to overcome activation barriers in addition to the Nernstian potential. Mass transfer analysis balanced conductivity and desorption efficiency, with a 1:1 ratio identified as optimal for redox-active species and background electrolyte concentration. To further enhance the kinetics of the redox reactions, plasma treatment of electrode surfaces was implemented, resulting in a 43% decrease in charge transfer resistance, as measured by electrochemical impedance spectroscopy (EIS) analysis. Finally, a bench-scale operation of the system demonstrated an energy consumption of 54 kJ/mol CO2, which is competitive with other electrochemical carbon capture technologies. Besides its energy competitiveness, the process offers multiple additional advantages, including the elimination of precious metal electrodes, oxygen insensitivity in flue gas, scalability inspired by VRFB technology, and the unique ability to function as a battery during the absorbent regeneration process, enabling efficient day-night operation.

ACS ES&T EngineeringVol. 5(5)
Division of Materials Science and Engineering (AU), University of Houston (US)
University of Houston, Office of Fossil Energy and Carbon Management, Division of Chemical, Bioengineering, Environmental, and Transport Systems
Openalex Percentile: Top 5%
Carbon Dioxide Capture Technologies
4.99
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.