A High Capacity Gas Diffusion Electrode for Li-O<sub>2</sub> Batteries.
basic_science · Level V
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- Record sourced from PubMed, PMID 39101286.
- Also identified by DOI 10.1002/adma.202405715.
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Abstract
The very high theoretical specific energy of the lithium-air (Li-O<sub>2</sub>) battery (3500 Wh kg<sup>-1</sup>) compared with other batteries makes it potentially attractive, especially for the electrification of flight. While progress has been made in realizing the Li-air battery, several challenges remain. One such challenge is achieving a high capacity to store charge at the positive electrode at practical current densities, without which Li-air batteries will not outperform lithium-ion. The capacity is limited by the mass transport of O<sub>2</sub> throughout the porous carbon positive electrode. Here it is shown that by replacing the binder in the electrode by a polymer with the intrinsic ability to transport O<sub>2</sub>, it is possible to reach capacities as high as 31 mAh cm<sup>-2</sup> at 1 mA cm<sup>-2</sup> in a 300 µm thick electrode. This corresponds to a positive electrode energy density of 2650 Wh L<sup>-1</sup> and specific energy of 1716 Wh kg<sup>-1</sup>, exceeding significantly Li-ion batteries and previously reported Li-O<sub>2</sub> cells. Due to the enhanced oxygen diffusion imparted by the gas diffusion polymer, Li<sub>2</sub>O<sub>2</sub> (the product of O<sub>2</sub> reduction on discharge) fills a greater volume fraction of the electrode and is more homogeneously distributed.