Multiscale Co‐Assembly to Meso‐Macroporous Foamed Single‐Crystal Metal–Organic Frameworks for the Supported Capture of Sulfur Dioxide

Author:

Kan Xun12,Zhang Guanqing1,Ma Jun3,Liu Fengqing4,Tang Yu5,Liu Fujian12ORCID,Yi Xianfeng4,Liu Yuefeng3,Zheng Anmin4,Jiang Lilong12,Xiao Feng‐Shou6,Dai Sheng7

Affiliation:

1. National Engineering Research Center of Chemical Fertilizer Catalyst (NERC‐CFC) School of Chemical Engineering Fuzhou University Fuzhou 350002 China

2. Qingyuan Innovation Laboratory Quanzhou Fujian 362801 P.R. China

3. Dalian National Laboratory for Clean Energy (DNL) Dalian Institute of Chemical Physics Chinese Academy of Science Dalian 116023 China

4. Wuhan Center for Magnetic Resonance, Key Laboratory of Magnetic Resonance in Biological Systems State Key Laboratory of Magnetic Resonance and Atomic and Molecular Physics Wuhan Institute of Physics and Mathematics Chinese Academy of Sciences Wuhan 430071 China

5. Institute of Molecular Catalysis and In‐situ/Operando Studies of Catalysis and State Key Laboratory of Photocatalysis on Energy and Environment and College of Chemistry Fuzhou University. Fuzhou 350116 China

6. Key Lab of Biomass Chemical Engineering of Ministry of Education College of Chemical and Biological Engineering Zhejiang University Hangzhou China

7. Chemical Sciences Division Oak Ridge National Laboratory Oak Ridge TN 37831 USA

Abstract

AbstractThe introduction of enlarged and interconnected nanochannels into metal–organic frameworks (MOFs) overcome their micropore size restriction, enhances mass transportation, and improves the accessibility of anchored metal clusters. Herein, foamed Ce‐MOF single crystals (F‐Ce‐MOF‐SC‐x) designed from a multiscale co‐assembly is reported in the presence of a copolymer template and 1,3,5‐trimethylbenzene as a structural regulator. The resultant F‐Ce‐MOF‐SC‐x possessed well‐defined microporous tandem‐ordered meso‐macroporous foams with superior connectivity and versatile Ce‐defective unsaturated sites (Ce‐DUS). F‐Ce‐MOF‐SC‐x is applied as a stable carrier for anchoring polytertiary amines (PA) via coordination interactions with Ce‐DUS. Owing to the superior ability of PA to recognize SO2, the resultant F‐Ce‐MOF‐SC‐x@yPA delivers exceptional performance in terms of the high‐temperature reversible adsorption and separation of SO2, including a remarkable capacity for SO2, spectacular selectivity for SO2/CO2/N2, an ultrafast adsorption equilibrium rate, and stability for 50 cycles. These characteristics are outstanding among those of MOFs and superior to those of many reported SO2 adsorbents.

Funder

National Natural Science Foundation of China

Publisher

Wiley

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