Abstract
A solid solution of magnesium and manganese borohydrides was studied by in situ synchrotron radiation X-ray powder diffraction and infrared spectroscopy. A combination of thermogravimetry, mass and infrared spectroscopy, and atomic emission spectroscopy were applied to clarify the thermal gas desorption of pure Mn(BH(4))(2) and a solid solution of composition Mg(0.5)Mn(0.5)(BH(4))(2).
Mg(x)Mn((1-x))(BH(4))(2) (x = 0-0.8) conserves the trigonal structure of Mn(BH(4))(2) at room temperature. Manganese is dissolved in the hexagonal structure of alpha-Mg(BH(4))(2), with the upper solubility limit not exceeding 10 mol.% at room temperature.
There exists a two-phase region of trigonal and hexagonal borohydrides within the compositional range x = 0.8-0.9 at room temperature. Infrared spectra show splitting of various vibrational modes, indicating the presence of two cations in the trigonal Mg(x)Mn((1-x))(BH(4))(2) solid solutions, as well as the appearance of a second phase, hexagonal alpha-Mg(BH(4))(2), at higher magnesium contents.
All vibrational frequencies are shifted to higher values with increasing magnesium content. The decomposition temperature of the trigonal Mg(x)Mn((1-x))(BH(4))(2) (x = 0-0.8) does not vary significantly as a function of the magnesium content (433-453 K).
The desorbed gas contains mostly hydrogen and 3-7.5 mol.% diborane B(2)H(6), as determined from analyses of the Mn(BH(4))(2) and Mg(0.5)Mn(0.5)(BH(4))(2) samples. An eutectic relation between alpha-Mg(BH(4))(2) and LiBH(4) is observed.
The solid solution Mg(x)Mn((1-x))(BH(4))(2) is a promising material for hydrogen storage as it decomposes at a similar temperature to Mn(BH(4))(2), i.e. at a much lower temperature than pure Mg(BH(4))(2) without significantly losing hydrogen weight capacity thanks to substitution of Mn by Mg up to 80 mol.%. The questions of diborane release and reversibility remain to be addressed.