Oriented 1D Metal–Organic Frameworks for Selective Chemisorption by a Substitution–Insertion Mechanism

• Published in: Nano letters Vol. 24; no. 41; pp. 12783 - 12790
• Main Authors: Sun, Qian, Du, Jingcheng, Song, Ziye, Yao, Ayan, Liu, Linghao, Ma, Ji, Cao, Dong, He, Wen, Hassan, Shabi Ul, Guan, Jian, Liu, Jiangtao
• Format: Journal Article
• Language: English
• Published: United States American Chemical Society 02-10-2024
• Subjects: reversible chemisorption; NH3 capture; coordination-responsive; alcohol−water separation; metal−organic framework
• ISSN: 1530-6984; 1530-6992; 1530-6992
• DOI: 10.1021/acs.nanolett.4c02921

Chemisorption on organometallic-based adsorbents is crucial for the controlled separation and purification of targeted systems. Herein, oriented 1D NH2-CuBDC·H2O metal–organic frameworks (MOFs) featuring accessible CuII sites are successfully fabricated by bottom-up interfacial polymerization. The prepared MOFs, as deliberately self-assembled secondary particles, exhibit a visually detectable coordination-responsive characteristic induced by the nucleophilic substitution and competitive coordination of guest molecules. As a versatile phase-change chemosorbent, the MOFs exhibit unprecedented NH3 capture (18.83 mmol g–1 at 298 K) and bioethanol dehydration performance (enriching ethanol from 99% to 99.99% within 10 min by direct adsorption separation of liquid mixtures of ethanol and water). Furthermore, the raw materials for preparing the 1D MOFs are inexpensive and readily available, and the facile regeneration with water washing at room temperature effectively minimizes the energy consumption and cost of recycling, enabling it to be the most valuable adsorbent for the removal and separation of target substances.