Destabilization of NaBH(4) by Transition Metal Fluorides

With the goal of improving performance of a hydrogen-rich storage medium, the influence of a collection of first and second period transition metal fluorides on the destabilization of NaBH(4) is studied on samples produced by ball milling NaBH(4) with 2 mol% of a metal fluoride additive. The effects obtained by increasing additive amount and changing oxidation state are also evaluated for NbF(5), CeF(3), and CeF(4). The as-milled products are characterized by in-house power X-ray diffraction, while the hydrogen release and decomposition are monitored by temperature programmed desorption with residual gas analysis, differential scanning calorimetry, and thermogravimetry. The screening of samples containing 2 mol% of additive shows that distinctive groups of transition metal fluorides affect the ball milling process differently depending on their enthalpy of formation, melting point, or their ability to react at the temperatures achieved during ball milling. This leads to the formation of NaBF(4) in the case of TiF(4), MnF(3), VF(4), CdF(2), NbF(5), AgF, and CeF(3) and the presence of the metal in CrF(3), CuF(2), and AgF. There is no linear correlation between the position of the transition metal in the periodic table and the observed behavior. The thermal behavior of the products after milling is given by the remaining NaBH(4), fluoride, and the formation of intermediate metastable compounds. A noticeable decrease of the decomposition temperature is seen for the majority of the products, with the exceptions of the samples containing YF(3), AgF, and CeF(3). The largest decrease of the decomposition temperature is observed for NbF(5). When comparing increasing amounts of the same additive, the largest decrease of the decomposition temperature is observed for 10 mol% of NbF(5). Higher amounts of additive result in the loss of the NaBH(4) thermal signal and ultimately the loss of the crystalline borohydride. When comparing additives with the same transition metal and different oxidation states, the most efficient additive is found to be the one with a higher oxidation state. Furthermore, among all the samples studied, higher oxidation state metal fluorides are found to be the most destabilizing agents for NaBH(4). Overall, the present study shows that there is no single parameter affecting the destabilization of NaBH(4) by transition metal fluorides. Instead, parameters such as the transition metal electronegativity and oxidation state or the enthalpy of formation of the fluoride and its melting point are competing to influence the destabilization. In particular, it is found that the combination of a high metal oxidation state and a low fluoride melting point will enhance destabilization. This is observed for MnF(3), NbF(5), NiF(2), and CuF(2), which lead to high gas releases from the decomposition of NaBH(4) at the lowest decomposition temperatures.