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.