Abstract
The substitution of the complex borohydride anion BH4− in calcium borohydride by the larger iodide anion I− is explored in order to tailor the hydrogen storage properties. Three new compounds are identified in the Ca(BH4)2−CaI2 system and are structurally characterized using the Rietveld method and synchrotron radiation powder X-ray diffraction (SR-PXD) data. Calcium borohydride readily dissolves in the trigonal calcium iodide structure during ball milling, forming a solid solution Ca((BH4)1−xIx)2 with a CaI2-type structure and an anisotropically contracted trigonal unit cell, a = 4.311(1) and c = 6.867(2) A for x ∼ 0.3 (T = 28 °C), space group P3m1. The trigonal tri-Ca((BH4)0.70I0.30)2 transforms at ∼180 °C to an orthorhombic phase of similar composition, ort-Ca((BH4)0.64I0.36)2, with a CaCl2-type structure (a distorted β-Ca(BH4)2 type structure) and cell parameters a = 7.271(2), b = 7.042(1), and c = 4.4601(7) A (T = 322 °C), space group Pnnm. Further heating of the CaCl2-type compound to ∼330 °C leads...
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