AX·(H 2 SeO 3 ) n (A = K, Cs; X = Cl, Br; n = 1, 2): A Series of Ionic Cocrystals as Promising UV Birefringent Materials with Large Birefringence and Wide Band Gap.

The design and syntheses of new birefringent crystals will be of great importance in commercial applications and materials science. A series of ultraviolet (UV) birefringent crystals, AX·(H 2 SeO 3 ) n (A = K, Cs; X = Cl, Br; n = 1, 2), with large sizes up to 23 × 6 × 3 mm 3 , was successfully synthesized by simple aqueous solution method. These four compounds belong to three different space groups. Isomorphic KCl·(H 2 SeO 3 ) 2 and CsCl·(H 2 SeO 3 ) 2 crystallize in the P 1 ¯ space group, while CsBr·(H 2 SeO 3 ) 2 and CsCl·H 2 SeO 3 crystallize in the P 2 1 / m and P 2 1 / c space groups, respectively. They exhibit cocrystal structures composed of [2(H 2 SeO 3 )] ∞ and [AX] ∞ frameworks, ingeniously inheriting the large optical anisotropy of selenite and the wide band gap of alkali metal halide. And it proves that these compounds indeed possess large birefringence (0.1-0.17 at 532 nm) and short UV cutoff edges (227-239 nm), achieving a balance of optical properties. This research affords a simple and viable strategy for the design and syntheses of new UV birefringent crystals. Besides, it is also found that the n value and ionic size (A and X ions) have important influences on the crystal structures and optical properties of AX·(H 2 SeO 3 ) n . And this will promote further understanding of the alkali metal halide selenite family.