Additives Capable of Stably Supplying Anions/Cations for Homogeneous Lithium Deposition/Stripping.
basic_science · Level V
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- Record sourced from PubMed, PMID 39636256.
- Also identified by DOI 10.1021/acsnano.4c13229.
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Abstract
One of the important factors leading to lithium dendrites is a slow lithium-ion mass transport and imbalanced distribution of the Li<sup>+</sup> concentration and nuclei sites on the anode surface. To achieve uniform lithium deposition during the charge and discharge process, we introduce a homemade new copolymer (with the quaternary ammonium group N<sub>3</sub>R<sup>+</sup>I<sup>-</sup> on its side chain as the main functional group), named P35, as a functional electrolyte additive to regulate the lithium deposition. Theoretical calculations show that under the strong coordinating interaction between I<sup>-</sup> and N<sub>3</sub>R<sup>+</sup>, P35 preferentially adsorbs onto the lithium foil surface, effectively countering the adsorption of lithium salt anions such as PF<sub>6</sub><sup>-</sup>. Moreover, the positive charge carried by the quaternary ammonium salt group of P35 could interact with PF<sub>6</sub><sup>-</sup> to limit their mobility. Consequently, the dipole interaction on lithium ions is diminished, leading to an enhancement in the transport rate and a decrease in the concentration gradient of lithium ions. Furthermore, a more efficient SEI was formed due to the dual charges electrostatic shield formed by N<sub>3</sub>R<sup>+</sup>I<sup>-</sup>. Li-Li symmetric cells and Li-LiFePO<sub>4</sub> full cells assembled with electrolytes with P35 exhibit better rate performance, smaller polarization, and smoother deposition morphology in comparison to the cells without the P35 additive.