Reactive capture of CO 2 via amino acid

• Published in: Nature communications Vol. 15; no. 1; p. 7849
• Main Authors: Xiao, Yurou Celine, Sun, Siyu Sonia, Zhao, Yong, Miao, Rui Kai, Fan, Mengyang, Lee, Geonhui, Chen, Yuanjun, Gabardo, Christine M, Yu, Yan, Qiu, Chenyue, Guo, Zunmin, Wang, Xinyue, Papangelakis, Panagiotis, Huang, Jianan Erick, Li, Feng, O'Brien, Colin P, Kim, Jiheon, Han, Kai, Corbett, Paul J, Howe, Jane Y, Sargent, Edward H, Sinton, David
• Format: Journal Article
• Language: English
• Published: England 08-09-2024
• EISSN: 2041-1723

Reactive capture of carbon dioxide (CO
) offers an electrified pathway to produce renewable carbon monoxide (CO), which can then be upgraded into long-chain hydrocarbons and fuels. Previous reactive capture systems relied on hydroxide- or amine-based capture solutions. However, selectivity for CO remains low (<50%) for hydroxide-based systems and conventional amines are prone to oxygen (O
) degradation. Here, we develop a reactive capture strategy using potassium glycinate (K-GLY), an amino acid salt (AAS) capture solution applicable to O
-rich CO
-lean conditions. By employing a single-atom catalyst, engineering the capture solution, and elevating the operating temperature and pressure, we increase the availability of dissolved in-situ CO
and achieve CO production with 64% Faradaic efficiency (FE) at 50 mA cm
. We report a measured CO energy efficiency (EE) of 31% and an energy intensity of 40 GJ t
, exceeding the best hydroxide- and amine-based reactive capture reports. The feasibility of the full reactive capture process is demonstrated with both simulated flue gas and direct air input.