The potassium storage performance
of UiO-66 derivatives was investigated
by density functional theory calculations. The calculation results
show that the substitution of all Zr in nodes of UiO-66 by Ti reduces
the band gap. During potassiation, UiO-66-Ti and UiO-66-Hf have similar
charge transfer processes to UiO-66, in which the charges of Ti and
Hf are almost not changed, and the charge transfers from K to C or
O near it. Compared with UiO-66, UiO-66-Hf has a lower theoretical
capacity (490 mAh/g) with a smaller volume expansion and a slightly
higher energy barrier for K-ion diffusion. UiO-66-Ti has a lower diffusion
barrier for K ion although it has a larger volume expansion with all
sites occupied by K. For the −NH2, −NO2, −Br, −Cl, −OH, −SH, and −CH3 functionalized UiO-66, the substitutions of H in ligands
reduce the band gap of UiO-66, with the largest reduction in UiO-66-NH2. The p orbitals of N in the NH2 contribute greatly
to the reduction of the band gap. The K intercalated at the K2(L)
and K3 sites during the charging process will transfer part of the
electrons to the substituents. Between the Zr6O4(OH)4 nodes, there will be a migration path that crosses
the substituent, and the diffusion energy barrier on this path is
smaller than that of the original path of UiO-66. The results suggest
that proper modification of UiO-66 can improve its electronic conductivity
and ionic conductivity as the anode of potassium ion battery.