膜
萃取(化学)
材料科学
化学工程
卤水
吸附
石墨烯
传质
渗透
选择性
浓差极化
水化能
位阻效应
动能
无机化学
化学
电动势
密度泛函理论
MXenes公司
互连性
门控
炭黑
单层
吉布斯自由能
离子
非平衡态热力学
半透膜
动力学
色谱法
羧甲基纤维素
平均力势
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
卷期号:19 (40): 35483-35492
被引量:2
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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