Photoassisted Li–CO<sub>2</sub> Batteries withUltrahigh Energy Efficiency and Cycle Stability by a Redox Mediator

Li–CO<sub>2</sub> batteries are considered promising energy storage systems for implementation in space applications. However, unsatisfactory overpotentials and poor cycling stability caused by the sluggish reaction kinetics of CO<sub>2</sub> reduction and evolution have greatly limited the practical application of Li–CO<sub>2</sub> batteries. Herein, we introduce a redox mediator LiI to stabilize the Bi<sub>5</sub>O<sub>7</sub>I photocathode by the successive separation of electrons and holes to accelerate the sluggish kinetics. Under illumination, LiI allows photogenerated holes to preferentially react with I<sup>–</sup> in the solid–liquid interface, thereby inhibiting the release of I<sup>–</sup> from Bi<sub>5</sub>O<sub>7</sub>I and effectively improving the lifespan of the photocathode. Thus, a high discharging platform of 3.05 V and an ultralow charging platform of 3.09 V are achieved to exhibit an energy efficiency of 98.8%. Moreover, a significantly enhanced reversibility is attained, attributed to the decomposition of Li<sub>2</sub>CO<sub>3</sub>, which further extends the cycle life to 250 h. This double-phase catalytic strategy demonstrates effectiveness in the development of high-performance Li–CO<sub>2</sub> batteries and other energy storage devices.

Publication Details

Journal
Figshare
Published
2025-02-20
DOI
https://doi.org/10.1021/acsnano.4c11559.s001
Primary Topic
Advanced Battery Materials and Technologies
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article
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article

Photoassisted Li–CO2 Batteries withUltrahigh Energy Efficiency and Cycle Stability by a Redox Mediator

Figshare
Advanced Battery Materials and Technologies
article

Photoassisted Li–CO2 Batteries withUltrahigh Energy Efficiency and Cycle Stability by a Redox Mediator

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Abstract

Li–CO<sub>2</sub> batteries are considered promising energy storage systems for implementation in space applications. However, unsatisfactory overpotentials and poor cycling stability caused by the sluggish reaction kinetics of CO<sub>2</sub> reduction and evolution have greatly limited the practical application of Li–CO<sub>2</sub> batteries. Herein, we introduce a redox mediator LiI to stabilize the Bi<sub>5</sub>O<sub>7</sub>I photocathode by the successive separation of electrons and holes to accelerate the sluggish kinetics. Under illumination, LiI allows photogenerated holes to preferentially react with I<sup>–</sup> in the solid–liquid interface, thereby inhibiting the release of I<sup>–</sup> from Bi<sub>5</sub>O<sub>7</sub>I and effectively improving the lifespan of the photocathode. Thus, a high discharging platform of 3.05 V and an ultralow charging platform of 3.09 V are achieved to exhibit an energy efficiency of 98.8%. Moreover, a significantly enhanced reversibility is attained, attributed to the decomposition of Li<sub>2</sub>CO<sub>3</sub>, which further extends the cycle life to 250 h. This double-phase catalytic strategy demonstrates effectiveness in the development of high-performance Li–CO<sub>2</sub> batteries and other energy storage devices.

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