Routes to Bidirectional Cathodes for Reversible Aprotic Alkali Metal-CO<sub>2</sub> Batteries.
review · Level V
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- Record sourced from PubMed, PMID 39308193.
- Also identified by DOI 10.1002/adma.202410704.
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Abstract
Aprotic alkali metal-CO<sub>2</sub> batteries (AAMCBs) have garnered significant interest owing to fixing CO<sub>2</sub> and providing large energy storage capacity. The practical implementation of AAMCBs is constrained by the sluggish kinetics of the CO<sub>2</sub> reduction reaction (CO<sub>2</sub>RR) and the CO<sub>2</sub> evolution reaction (CO<sub>2</sub>ER). Because the CO<sub>2</sub>ER and CO<sub>2</sub>RR take place on the cathode, which connects the internal catalyst with the external environment. Building a bidirectional cathode with excellent CO<sub>2</sub>ER and CO<sub>2</sub>RR kinetics by optimizing the cathode's internal catalyst and environment has attracted most of the attention to improving the electrochemical performance of AAMCBs. However, there remains a lack of comprehensive understanding. This review aims to give a route to bidirectional cathodes for reversible AAMCBs, by systematically discussing engineering strategies of both the internal catalyst (atomic, nanoscopic, and macroscopic levels) and the external environment (photo, photo-thermal, and force field). The CO<sub>2</sub>ER and CO<sub>2</sub>RR mechanisms and the "engineering strategies from internal catalyst to the external environment-cathode properties-CO<sub>2</sub>RR and CO<sub>2</sub>ER kinetics and mechanisms-batteries performance" relationship are elucidated by combining computational and experimental approaches. This review establishes a fundamental understanding for designing bidirectional cathodes and gives a route for developing reversible AAMCBs and similar metal-gas battery systems.