Protection of High-Nickel Cathodes from H<sub>2</sub>O-Triggered Electrochemical Degradation Enabled by Moisture-Responsible Dehumidifying Separators.
basic_science · Level V
Where this comes from
- Record sourced from PubMed, PMID 41680103.
- Also identified by DOI 10.1021/acsnano.5c19443.
- No licence information is recorded for this record.
- Because redistribution is not established, this page shows the abstract only. Follow the links below for the full text.
Abstract
High-Ni NCM (LiNi<sub><i>x</i></sub>Co<sub><i>y</i></sub>Mn<sub><i>z</i></sub>O<sub>2</sub>) has been widely adopted as a promising solution for enhancing the energy density of lithium-ion batteries (LIBs) owing to its high theoretical specific capacity and wide operating voltage. Because of the high oxidation stability, a carbonate electrolyte containing LiPF<sub>6</sub> salt is employed in such a battery system; however, LiPF<sub>6</sub> reacts with the residual moisture, which remains even after thorough drying processes, to produce detrimental hydrofluoric acid (HF) promoting the significant structural degradation of high-Ni NCM. Herein, a moisture-responsive dehumidifying separator incorporating an oxygen-deficient TiO<sub>2-<i>x</i></sub> nanolayer was developed to mitigate the water-induced electrochemical degradation of LIBs paired with high-Ni NCM cathodes, thereby stabilizing the electrochemical performance even under highly humid conditions. Owing to the advantageous characteristics of the oxygen-deficient TiO<sub>2-<i>x</i></sub>, which spontaneously transforms into TiO<sub>2</sub> by reacting with moisture, LIBs employing the TiO<sub>2-<i>x</i></sub>/PE separator achieved a stable electrochemical performance even under extreme conditions of high H<sub>2</sub>O concentration and high cutoff voltage by suppressing the H<sub>2</sub>O-induced electrochemical deterioration. This dehumidifying separator would expedite the commercialization of the LIBs using high-Ni NCM and LiPF<sub>6</sub>-based electrolyte by mitigating the electrochemical degradation of electrodes caused by residual H<sub>2</sub>O.