Coupling electrochemical CO2 conversion with CO2 capture
Ian Sullivan (California Institute of Technology)
A. Goryachev (TU Delft - ChemE/Transport Phenomena)
Ibadillah A. Digdaya (California Institute of Technology)
Xueqian Li (California Institute of Technology)
Harry A. Atwater (California Institute of Technology)
David Vermaas (TU Delft - ChemE/Transport Phenomena)
Chengxiang Xiang (California Institute of Technology)
More Info
expand_more
Abstract
Electrochemical CO2 conversion into fuels or chemicals and CO2 capture from point or dilute sources are two important processes to address the gigaton challenges in reducing greenhouse gas emissions. Both CO2 capture and electrochemical CO2 conversion are energy intensive, and synergistic coupling between the two processes can improve the energy efficiency of the system and reduce the cost of the reduced products, via eliminating the CO2 transport and storage or eliminating the capture media regeneration and molecular CO2 release. We consider three different levels to couple electrochemical CO2 reduction with CO2 capture: independent (Type-I), subsequent (Type-II) and fully integrated (Type-III) capture and conversion processes. We focus on Type-II and Type-III configurations and illustrate potential coupling routes of different capture media, which include amine-based solutions and direct carbamate reduction, redox active carriers, aqueous carbonate and bicarbonate solutions, ionic liquids CO2 capture and conversion mediated by covalent organic frameworks. [Figure not available: see fulltext.]
No files available
Metadata only record. There are no files for this record.