A first-principles study of the electronic structure and stability of Be(BH4)2

TL;DR

This study uses first-principles calculations to analyze the electronic structure and stability of beryllium boranate, revealing its unique hydrogen desorption pathway and low formation enthalpy, relevant for hydrogen storage applications.

Contribution

It provides the first detailed electronic and thermodynamic analysis of Be(BH4)2, highlighting its distinct desorption mechanism and low stability compared to other boranates.

Findings

Hydrogen desorption likely occurs directly to elements.

Formation enthalpy is only -0.12 eV/H2, indicating low stability.

Decomposition temperature estimated at 162 K at 1 bar.

Abstract

Alanates and boranates are studied intensively because of their potential use as hydrogen storage materials. In this paper we present a first-principles study of the electronic structure and the energetics of beryllium boranate, Be(BH4)2. From total energy calculations we show that - in contrast to the other boranates and alanates - hydrogen desorption directly to the elements is likely, and is at least competitive with desorption to the elemental hydride (BeH2). The formation enthalpy of Be(BH4)2 is only -0.12 eV/H2 (at T=0K). This low value can be rationalized by the participation of all atoms in the covalent bonding, in contrast to the ionic bonding observed in other boranates. From calculations of thermodynamic properties at finite temperature we estimate a decomposition temperature of 162 K at a pressure of 1 bar.