Self‐Assembled Nanoporous Metal–Organic Framework Monolayer Film for Osmotic Energy Harvesting
Jie Xiaoa b c d, Muyu Conge f, Minmin Lia c, Xin Zhanga c, Yahui Zhanga c, Xinjia Zhaoa c, Wenqi Lua b c d, Zhimou Guoa c, Xinmiao Lianga c✉, Guangyan Qinga c✉
- aCAS Key Laboratory of Separation Science for Analytical Chemistry Dalian Institute of Chemical Physics Chinese Academy of Sciences Dalian 116023 P. R. China
- bUniversity of Chinese Academy of Sciences Beijing 100049 P. R. China
- cCAS Key Laboratory of Separation Science for Analytical Chemistry, Dalian Institute of Chemical Physics, Chinese Academy of Sciences, Dalian, 116023 P. R. China
- dUniversity of Chinese Academy of Sciences, Beijing, 100049 P. R. China
- eInstitute of Fine Chemicals School of Chemistry and Molecular Engineering East China University of Science and Technology Shanghai 200237 P. R. China
- fInstitute of Fine Chemicals, School of Chemistry and Molecular Engineering, East China University of Science and Technology, Shanghai, 200237 P. R. China
- ✉Corresponding author
Papers open inside SciRah from the original publisher or repository; SciRah never hosts them.
Abstract
Abstract Osmotic energy represents a promising energy resource because it is sustainable and environmentally benign. Subnanoscale channels are considered as a competitive platform for generating this blue energy due to their highly selective and ultrafast ion transport. However, fabricating functional subnanochannels capable of high energy output remains challenging. Here, a heterogeneous subnanochannel membrane formed by coating a functionalized self‐assembled metal−organic framework (MOF) monolayer (SAMM) film on a porous anodic aluminum oxide membrane, is reported. The SAMM film, with a thickness of ≈160 nm, is fabricated by self‐assembly of poly(methyl methacrylate‐ co ‐vinylimidazole)‐modified UiO‐66‐NH 2 nanoparticles at the water−air interface. In the SAMM, imidazole and NH 2 groups provide abundant positive charges, while the angstrom‐scale windows act as ionic filters for selective screening of anions with different hydration diameters. As a result, the heterogeneous membrane exhibits excellent capacity for anion‐selective transport, which contributes to an optimal osmotic power of 6.76 W m −2 under a 100‐fold NaCl gradient, as well as a high Cl − /SO 4 2− selectivity of ≈42.2. Further, the output power is increased to 10.5 W m −2 by methylating imidazole moieties on the MOF surface. This work provides a facile and modular approach to fabricate subnanochannels for enabling highly selective and efficient osmotic energy conversion.

