膜
化学工程
材料科学
氢氧化物
渗透
异质结
纳米孔
层状结构
化学稳定性
纳米技术
化学
复合材料
渗透
光电子学
生物化学
工程类
作者
Yahua Lu,Miao Zhang,Jian Chang,Anirban Sikdar,Naixin Wang,Quan‐Fu An,Jiayin Yuan
标识
DOI:10.1016/j.memsci.2023.122100
摘要
Two-dimensional (2D) MXene-based lamellar membranes play transformative roles in membrane filtration technology. Their practical use in water treatment is however hindered by several hurdles, e.g., unfavorable swelling due to weak interactions between adjacent MXene nanosheets, tortuous diffusion pathways of layered stacking, and the intrinsic aquatic oxidation-prone nature of MXene. Herein, nanoporous 2D/2D heterostructure membranes are elaborately constructed via solution-phase assembly of oppositely charged MXene and modified layered double hydroxide (MLDH) nanosheets. As a multifunctional component, positively charged holey MLDH nanosheets were first tailor-made to serve simultaneously as a binder, spacer and surface-modifier; next they were intercalated into negatively charged MXene lamella to enhance structural stability and mass transfer of membranes. As a result, the as-prepared MLDH@MXene heterostructure membranes successfully break the persistent trade-off between high permeability and selectivity while mitigating the common drawbacks in 2D MXene-based lamellar membranes, e.g., swelling issues, restacking problems, and vulnerable chemical stability. Noticeably, at an operating pressure of 4 bar and a feed solution of 100 ppm of Congo red, the heterostructure membranes enable a threefold jump in permeability (332.7 ± 20 L m-2 h-1 bar-1) when compared to the pristine MXene membrane (119.3 ± 18 L m-2 h-1 bar-1), and better operational stability without compromising the rejection.
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