Activated Co in Thiospinel Boosting Li<sub>2</sub>CO<sub>3</sub> Decomposition in Li-CO<sub>2</sub> Batteries.
basic_science · Level V
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- Record sourced from PubMed, PMID 39177199.
- Also identified by DOI 10.1002/adma.202406856.
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Abstract
Catalytic reactions mainly depend on the adsorption properties of reactants on the catalyst, which provides a perspective for the design of reversible lithium-carbon dioxide (Li-CO<sub>2</sub>) batteries including CO<sub>2</sub> reduction (CO<sub>2</sub>RR) and CO<sub>2</sub> evolution (CO<sub>2</sub>ER) reactions. However, due to the complex reaction process, the relationship between the adsorption configuration and CO<sub>2</sub>RR/CO<sub>2</sub>ER catalytic activity is still unclear in Li─CO<sub>2</sub> batteries. Herein, taking Co<sub>3</sub>S<sub>4</sub> as a model system, nickel (Ni substitution in the tetrahedral site to activate cobalt (Co) atom for forming multiatom catalytic domains in NiCo<sub>2</sub>S<sub>4</sub> is utilized. Benefiting from the special geometric and electronic structures, NiCo<sub>2</sub>S<sub>4</sub> exhibits an optimized adsorption configuration of lithium carbonate (Li<sub>2</sub>CO<sub>3</sub>), promoting its effective activation and decomposition. As a result, the Li-CO<sub>2</sub> batteries with NiCo<sub>2</sub>S<sub>4</sub> cathode exhibit remarkable electrochemical performance in terms of low potential gap of 0.42 V and high energy efficiency of 88.7%. This work provides a unique perspective for the development of highly efficient catalysts in Li-CO<sub>2</sub> batteries.