Ongoing studies of the CsHSO 4 ±CsH 2 PO 4 system, aimed at developing novel proton conducting solids, resulted in the new compound Cs 2 (HSO 4 )(H 2 PO 4 ) (dicesium hydrogensulfate dihydrogenphosphate). Single-crystal X-ray diffraction (performed at room temperature) revealed Cs 2 (HSO 4 )(H 2 PO 4 ) to crystallize in space group P2 1 /n with lattice parameters a = 7.856 (8), b = 7.732 (7), c = 7.827 (7) A Ê , and = 99.92 (4). The compound has a unit-cell volume of 468.3 (8) A Ê 3 and two formula units per cell, giving a calculated density of 3.261 Mg m
À3. Six non-H atoms and two H atoms were located in the asymmetric unit, with SO 4 and PO 4 groups randomly arranged on the single tetrahedral anion site. Re®nement using all observed re¯ections yielded weighted residuals of 0.0890 and 0.0399 based on F 2 and F values, respectively. Anisotropic temperature factors were employed for all six non-H atoms and ®xed isotropic temperature factors for the two H atoms. The structure contains zigzag chains of hydrogen-bonded anion tetrahedra that extend in the [010] direction. Each tetrahedron is additionally linked to a tetrahedron in a neighboring chain to give a planar structure with hydrogen-bonded sheets lying parallel to (1 Å 01). Thermal analysis of the superprotonic transition in Cs 2 (HSO 4 )(H 2 PO 4 ) showed that the transformation to the high-temperature phase occurs by a two-step process. The ®rst is a sharp transition at 334 K and the second a gradual transition from 342 to 378 K. The heat of transformation for the entire process ($330±382 K) is 44 AE 2 J g
À1. Thermal decomposition of Cs 2 (HSO 4 )(H 2 PO 4 ) takes place at much higher temperatures, with an onset of approximately 460 K.