Tuning Water Transport through Nanochannels of Robust Cation‐Intercalated Ti3C2Tx MXene Membranes

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Abstract
Ti3C2Tx MXene membranes have attracted considerable interest due to their exceptional water transport properties, yet the role of cation intercalation on governing transport remains poorly understood. In this experimental and theoretical study, it shows how intercalation with K+, Na+, Li+, Ca2+, and Mg2+ modulates both the nanochannel architecture and water flux of Ti3C2Tx membranes. Unlike in graphene oxide analogs, cations with larger hydration diameters in Ti3C2Tx expand the interlayer spacing, widening flow channels, enhancing slip length of these nanochannels, and boosting water flux from 31.45 to 61.86 L m−2 h−1. To overcome intrinsically poor adhesion of Ti3C2Tx to polymeric supports, this study incorporates a thin polyvinyl‐alcohol interlayer, which substantially enhances mechanical robustness and structural integrity. Together, these findings elucidate how cation hydration controls water transport and offer a flexible strategy for tailoring MXene membrane performance.

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