膜
纤维素
萃取(化学)
材料科学
化学工程
锂(药物)
细菌纤维素
无机化学
化学
色谱法
生物化学
医学
工程类
内分泌学
作者
Kou Yang,Qinyue Wang,Konstantin G. Nikolaev,Qian Wang,Ivan V. Moskalenko,Shanqing Zhang,Xueqing Qiu,E.O. Timashev,Ekaterina V. Skorb,Kostya S. Novoselov,Daria V. Andreeva
出处
期刊:ACS Nano
[American Chemical Society]
日期:2025-10-02
标识
DOI:10.1021/acsnano.5c08653
摘要
A nanoconfined thermoresponsive membrane composed of Ti3C2Tx MXene and hydroxypropyl cellulose (HPC) was developed for selective Li+ extraction. By integrating the electrothermal conductivity of MXenes and hydration-responsive gating of HPC, the membrane forms heterochannels with tunable spacing that regulate ion transport through nanoconfinement-enhanced mechanisms based on interaction energy and hydration radius. While density functional theory calculations predicted stronger sorption for Mg2+, experimental data revealed a clear preference for Li+ uptake from both simulated brine and battery black mass. This selectivity is attributed to favorable interactions of Li+ within the nanoconfined composite channels, where the subnanometer interlayer spacings promote partial dehydration and size-sieving effects. Li+ retention is governed not only by thermodynamic affinity but also by kinetic acceleration in nanoconfined pathways and hydration-based steric control. The membrane exhibits a reversible thermal response and maintains stable performance under Joule heating. It achieves >90% extraction efficiency from simulated Atacama brine and up to 98% Li+ recovery from black mass supplied by VGM Sustainability Solutions (SG3R, Pte. Ltd.).
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