Unravelling the Synergistic Effect of Multiscale Hierarchical Material Architecture for Enhanced Urea Adsorption

Abstract

Adsorption of inert small molecules has always been challenging, and hence, these molecules are generally difficult to remove from solution. In this work, we demonstrated a significant improvement (>25 times) in the adsorption of an inert small molecule, urea, using a hierarchical material design, which remarkably outperformed the simple chemical functionalization of the substrate. To illustrate this point, we employed two-dimensional (2D) materials such as Ti₃C₂T_x MXene as the adsorbent “substrate” which has a high potential for efficient urea removal. In particular, Cu-functionalized MXene, with Cu valency between 0 and +1 exhibited superior urea adsorption performance compared to pristine MXene. However, due to the strong van der Waals forces, MXene has a propensity to aggregate, leading to the loss of active sites for urea adsorption. To address this, cellulose nanocrystals were introduced as they have dual functionalities, namely, to prevent aggregation and preserve active sites for adsorption of urea. These nanocrystals are small, rigid, and hydrophilic, facilitating their interaction with hydrophilic groups on the MXene surface. Porous hydrogel macrobeads prepared using alginate cross-linked with calcium ions yielded a hierarchical structure with nanosized MXene-cellulose moieties distributed within the millimeter beads. Besides serving as mechanical support, the cellulose nanocrystals can be further surface-functionalized with enhanced interaction with chemical groups such as polydopamine to boost the adsorption properties. Each component in the hydrogel composite synergistically enhanced the interaction with urea and promoted adsorption. Consequently, the composite hydrogel exhibited a remarkable enhancement in urea adsorption capacity from 6.7 to 354.4 mg/g in aqueous solution, while a maximum adsorption capacity (Q_max) of 115.1 mg/g was observed in simulated dialysate solution due to the increased surface area available for urea adsorption. The development of this hydrogel composite consisting of Cu-functionalized MXene, functionalized cellulose nanocrystals, and alginate cross-linked with calcium showcased its potential as a highly efficient and versatile material for effective urea adsorption in both aqueous and simulated dialysate solutions.