Pseudo-trilayer Organoclay Enables Directed Li<sup>+</sup> Transport and Anion Trapping in Quasi-Solid-State Gel Electrolytes.

Choi, Young Gyun; Kim, Jongkyoung; Park, Chanui; Jang, Jin Il; Kim, Sangdeok; Kim, Hyoseok; Kim, Hyung Min; Lee, Won Bo et al. · ACS Nano · 2025

basic_science · Level V

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Abstract

Enhancing Li<sup>+</sup> transport while ensuring safety is crucial for the development of high-energy density batteries. While nanomaterials boost ionic conductivity in quasi-solid state gel electrolyte (QSE), the transport mechanisms remain unclear. This study presents a synthetic strategy utilizing tailored two-dimensional saponite clay additives with a controlled organic cation configuration to achieve superior Li-ion conductivity in QSE. This optimized configuration enables rapid, uniform Li<sup>+</sup> movement through controlled interlayers and effective anion trapping within aligned surfactant domains. Consequently, a pseudo-trilayer configuration of organoclay serves as a fast Li<sup>+</sup> transport pathway in the QSE, leading to a high Li<sup>+</sup> transference number of 0.71 and stable cycling performance for 1000 h. Moreover, batteries utilizing the pseudo-trilayer organoclay demonstrate compatibility with the LiNi<sub>0.9</sub>Mn<sub>0.05</sub>Co<sub>0.05</sub>O<sub>2</sub> cathode, maintaining 86.7% capacity retention after 200 cycles. This work suggests a design strategy for advanced QSE that precisely controls the Li<sup>+</sup> transport route, contributing to a high energy density with minimal additives.