Experimental and theoretical studies of the LiBH-LiI phase diagram

• Published in: RSC advances 2024-04, Vol.14 (17), p.1238-1248
• Main Authors: Mazzucco, Asya, Dematteis, Erika Michela, Gulino, Valerio, Corno, Marta, Sgroi, Mauro Francesco, Palumbo, Mauro, Baricco, Marcello
• Format: Article
• ISSN: 2046-2069
• DOI: 10.1039/d4ra01642d

The hexagonal structure of LiBH 4 at room temperature can be stabilised by substituting the BH 4 − anion with I − , leading to high Li-ion conductive materials. A thermodynamic description of the pseudo-binary LiBH 4 -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(BH 4 ) 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 LiBH 4 -LiI phase diagram has been assessed and evaluated across all compositions and temperature ranges by applying the CALPHAD method. The hexagonal structure of LiBH 4 at room temperature can be stabilised by substituting the BH 4 − anion with I − , leading to high Li-ion conductive materials.