Exceptional Iodine Capture in 2D Covalent Organic Frameworks

Progress in chemistry over the past four decades has generated a variety of porous materials for removing iodinea radioactive emission accompanying nuclear fission. However, most studies are still based on the notion that entangled pores together with specific binding sites are essential for iodine capture. Here, an unraveled physical picture of iodine capture that overturns the preconception by exploring 1D channeled porous materials is disclosed. 2D covalent organic frameworks are constructed in a way so that they are free of interpenetration and binding sites but consist of 1D open channels. As verified with different channels shaping from hexagonal to tetragonal and trigonal and ranging from micropores to mesopores, all the 1D channels enable a full access to iodine, generalizing a new paradigm that the pore volume determines the uptake capacity. These results are of fundamental importance to understanding iodine uptake and designing materials to treat coagulative toxic vapors.