# Decomposition mechanisms in metal borohydrides and their ammoniates

## TL;DR

This study uses ab initio methods to understand how ammoniation affects decomposition mechanisms in metal borohydrides, revealing a shift from destabilization to stabilization around a specific electronegativity threshold, which influences hydrogen release behavior.

## Contribution

It provides a detailed mechanistic understanding of ammoniation effects in metal borohydrides, explaining the transition in decomposition pathways based on metal electronegativity.

## Key findings

- Ammoniation destabilizes low-electronegativity MBs, lowering decomposition temperatures.
- It blocks B2H6 formation in high-electronegativity MBs, stabilizing them.
- The shift in decomposition mechanism occurs around electronegativity 1.6.

## Abstract

Ammoniation in metal borohydrides (MBs) with the form $\mathcal{M}$(BH$_4$)$_x$ has been shown to lower their decomposition temperatures with $\mathcal{M}$ of low electronegativity ($\chi_p \lesssim 1.6$), but raise it for high-$\chi_p$ MBs ($\chi_p \gtrsim 1.6$). Although this behavior is just as desired, an understanding of the mechanisms that cause it is still lacking. Using \emph{ab initio} methods, we elucidate those mechanisms and find that ammoniation always causes thermodynamic destabilization, explaining the observed lower decomposition temperatures for low-$\chi_p$ MBs. For high-$\chi_p$ MBs, we find that ammoniation blocks B$_2$H$_6$ formation---the preferred decomposition mechanism in these MBs---and thus kinetically stabilizes those phases. The shift in decomposition pathway that causes the distinct change from destabilization to stabilization around $\chi_p=1.6$ thus coincides with the onset of B$_2$H$_6$ formation in MBs. Furthermore, with our analysis we are also able to explain why these materials release either H$_2$ or NH$_3$ gas upon decomposition. We find that NH$_3$ is much more strongly coordinated with higher-$\chi_p$ metals and direct H$_2$ formation/release becomes more favorable in these materials. Our findings are of importance for unraveling the hydrogen release mechanisms in an important new and promising class of hydrogen storage materials, allowing for a guided tuning of their chemistry to further improve their properties.