Experimental and theoretical studies of the LiBH4–LiI phase diagram†
a
Erika Michela
Dematteis,
a
Marta
Corno,
a
Mauro Francesco
Sgroi,
a
Mauro
Palumbo
a
and
Marcello
Baricco
*a
Abstract
The hexagonal structure of LiBH4 at room temperature can be stabilised by substituting the BH4− anion with I−, leading to high Li-ion conductive materials. A thermodynamic description of the pseudo-binary LiBH4–LiI system is presented. The system has been explored investigating several compositions, synthetized by ball milling and subsequently annealed. X-ray diffraction and Differential Scanning Calorimetry have been exploited to determine structural and thermodynamic features of various samples. The monophasic zone of the hexagonal Li(BH4)1−x(I)x solid solution has been experimentally defined equal to 0.18 ≤ x ≤ 0.60 at 25 °C. In order to establish the formation of the hexagonal solid solution, the enthalpy of mixing was experimentally determined, converging to a value of 1800 ± 410 J mol−1. Additionally, the enthalpy of melting was acquired for samples that differ in molar fraction. By merging experimental results, literature data and ab initio theoretical calculations, the pseudo-binary LiBH4–LiI phase diagram has been assessed and evaluated across all compositions and temperature ranges by applying the CALPHAD method.
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