Li-CO2 batteries demonstrate promising prospects in terms of high-density energy storage and efficient CO2 fixation. However, their practical application is impeded by sluggish reaction kinetics and leakage of volatile and flammable organic electrolytes, especially for high temperature application scenarios, leading to large polarization and limited cycling stability. Herein, we fabricate a highly rechargeable and stable Li-CO2 battery with high temperature adaptability by employing fluorine-substituted graphdiyne (FGDY) as cathode catalysts and imidazolium-based ionic liquid as electrolyte solvents. The employed FGDY, which possesses homogeneous sp-hybridized carbon, high specific surface area, and uniform pores, significantly enhances the battery reaction kinetics. Consequently, the fabricated Li-CO2 batteries operate consistently at a large current density of 5.0 A·g-1 at 80 °C while showcasing high discharge capacity of 29050 mAh·g-1 along with excellent cycling stability. As proof of concept, Li-CO2 pouch cells achieve a high energy density of 536 Wh·kg-1 based on the total mass of the device, and show outstanding cycling stability at 80 °C. This study underscores the effectiveness of graphdiyne-derived carbon catalysts in achieving high-performance Li-CO2 batteries.
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http://dx.doi.org/10.1002/anie.202420892 | DOI Listing |
Angew Chem Int Ed Engl
January 2025
University of Electronic Science and Technology of China, No.2006 Xiyuan Road, 611731, Chengdu, CHINA.
Li-CO2 batteries demonstrate promising prospects in terms of high-density energy storage and efficient CO2 fixation. However, their practical application is impeded by sluggish reaction kinetics and leakage of volatile and flammable organic electrolytes, especially for high temperature application scenarios, leading to large polarization and limited cycling stability. Herein, we fabricate a highly rechargeable and stable Li-CO2 battery with high temperature adaptability by employing fluorine-substituted graphdiyne (FGDY) as cathode catalysts and imidazolium-based ionic liquid as electrolyte solvents.
View Article and Find Full Text PDFACS Appl Mater Interfaces
January 2025
Department of Chemical and Biological Engineering, University of New Mexico, Albuquerque, New Mexico 87131, United States.
Rechargeable Li-CO batteries face challenges of sluggish reaction kinetics and poor rechargeability. Highly efficient electrocatalysts are urgently needed to decompose the discharge product, LiCO. Mn-based transition metal oxides are regarded as promising candidates for improving the cycle performance and reaction kinetics of Li-CO batteries.
View Article and Find Full Text PDFACS Nano
December 2024
State Key Laboratory of Organic-Inorganic Composites, Beijing Key Laboratory of Electrochemical Process and Technology for Materials, Beijing University of Chemical Technology, Beijing 100029, China.
MXenes are promising cathodes for Li-CO batteries owing to their high electrical conductivity and efficient CO activation function. However, the effects of adsorption and electronic structures of MXene on the full life cycle of Li-CO batteries have been rarely investigated. Here, we employ a coregulation approach to enhance the adsorption-decomposition of lithium carbonate (LiCO) by introducing Zn and Cl surface groups onto the TiC MXene (Zn-TiCCl) catalyst.
View Article and Find Full Text PDFNanomaterials (Basel)
November 2024
Department of Electronic and Information Materials Engineering, Division of Advanced Materials Engineering, Research Center of Advanced Materials Development, Jeonbuk National University, Jeonju 54896, Republic of Korea.
Li-CO batteries (LCBs) have emerged as promising solutions for energy storage, with the added benefit of contributing to carbon neutrality by capturing and utilizing CO during operation. In this study, a high-performance LCB was developed using a Ge-doped LiAlGeTi (PO) (LAGTP) solid electrolyte, which was synthesized via a solution-based method by doping Ge into NASICON-type LATP. The ionic conductivity of the LAGTP pellets was measured as 1.
View Article and Find Full Text PDFNano Lett
December 2024
State Key Laboratory of Organic-Inorganic Composites, College of Chemical Engineering, Beijing University of Chemical Technology, Beijing 100029, China.
Surface discharge mechanism-induced cathode passivation is a critical challenge that blocks the full liberation of the ultrahigh theoretical energy density of Li-CO batteries. Herein, we propose a novel concept based on Hansen solubility parameters (HSPs) to guide the selection of solvents for inducing the dissolution of discharge products, facilitating the detachment of in situ-formed metastable LiCO from the electrode surface and enabling a continuous LiCO-dominated discharge process. Combining theoretical calculations with HSP predictions, we identified Pd-OCNTs as an ideal catalyst, with tetraethylene glycol dimethyl ether as the optimal solvent for LiCO production and stabilization.
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