“…Metal–organic frameworks (MOFs) and its nanoscale form (NMOFs), constructed from inorganic metal nodes and organic ligands, represent a new subclass of highly crystallized and porous materials with structural and chemical versatility. , Benefiting from the large Brunauer–Emmett–Teller (BET) surface and adjustable pore size, MOFs have already been considered to be powerful platforms in gas storage and separation, , drug delivery systems, , catalysis, , and pollutant removal and decomposition. , For iodine capture, great progress has been made by using MOF-based adsorbents with high capture efficiency in different mechanisms . Unlike the physically molecular adsorption within the pore, the key for the iodine capture is to supply necessary micro-environments to enhance the affinity interaction between the MOF host and guest. , For examples, Nenoff et al suggested that the iodine capture within the sodalite (SOD) cage of ZIF-8 mainly ascribes to the favorable interaction of loading iodine molecules with the MeIM linker, which leads to a high 5.4 iodine molecules within each SOD cage . Similarly, a number of previous studies have indicated that the nitrogen-heterocycle imidazole and pyridine linkers or −NH 2 substituted linkers within MOF frameworks could be helpful to increase the content of iodine affinity via the charge-transfer effect, resulting in the high capability in iodine capture. − Additionally, the existing guest molecules within the pore of MOFs can be developed to improve the iodine capture, and much higher iodine adsorption of 3.4 g g –1 has been reported recently in the ionic liquid@PCN-333 by forming the dynamic ionic liquid–iodide anion complexes .…”