The development of low-cost and high-efficiency iodine sorbents is of great significance for the control of nuclear pollution. In this work, we intercalate the tin sulfide cluster of [Sn2S6]4- to Mg/Al-type layered double hydroxides to obtain Sn2S6-LDH, which exhibits highly efficient capture performance of iodine vapor and iodine in solutions. The dispersion effect of the positively charged LDH layers contributes to the adequate exposure of [Sn2S6]4- anions, providing plentiful adsorption sites. For iodine vapor, Sn2S6-LDH showed an extremely large iodine capture capacity of 2954 mg/g with a large contribution from physisorption. For iodine in solutions, a significantly large sorption capacity of 1308 mg/g was achieved. During iodine capture, I2 molecules were reduced to I- ions (by S2- in [Sn2S6]4-), which then reacted with Sn4+ to form SnI4, where the molar amount of captured iodine is 4-fold that of Sn. Besides, the as-reduced I- combined with I2 again to generate [I3]-, which then entered the LDH interlayers to maintain electric neutrality. While reducing iodine, S2- itself in [Sn2S6]4- was oxidized to S8, which further combined with SnI4 to form a novel compound of SnI4(S8)2. The excellent iodine capture capability endows Sn2S6-LDH with a promising application in trapping radioactive iodine.
Keywords: [Sn2S6]4− cluster; adsorption; intercalation; iodine; layered double hydroxide.