Structural phase stability, electronic structure, magnetic properties and chemical bonding analysis of transition metal ammine borohydrides with amphoteric hydrogen for hydrogen storage

TL;DR

This study investigates transition metal ammine borohydrides, revealing their unique amphoteric hydrogen behavior, magnetic properties, and potential for high-capacity hydrogen storage due to high hydrogen content and diffusion barriers.

Contribution

It demonstrates the coexistence of positive and negative oxidation states of hydrogen within the same structure and analyzes their magnetic and diffusion properties for energy storage.

Findings

Hydrogen exhibits amphoteric behavior, with different oxidation states near boron and nitrogen.

TMABHs have antiferromagnetic ground states.

Ammonia diffusion barriers exceed 1 eV, suitable for hydrogen storage.

Abstract

Usually the ions of a particular element in solids are in positive or negative oxidation states, depending upon the chemical environment. It is highly unusual for an atom having both positive as well as negative oxidation states simultaneously within the same structural framework in a particular compound. Our structural and chemical bonding analyses show that the hydrogen ions in the transition metal ammine borohydrides (TMABHs) with the chemical formula M(BH4)2(NH3)2 (M = Sc, Ti, V, Cr, Mn, Fe, Co, Ni, Cu and Zn) have both positive and negative oxidation states. Our detailed analyses confirm the amphoteric behaviour of hydrogen where hydrogen closer to boron is in negative oxidation state and that closer to nitrogen is in the positive oxidation state. From the spin polarised van der Waals interaction included calculation, we found that TMABHs has antiferromagnetic ordering as ground state. Our nudged elastic band calculation show that the migration barrier for ammonia diffusion in these materials are more than 1 eV and hence these compounds may be used for energy storage applications since they have high weight percentage of hydrogen. The presence of amphoteric behaviour of hydrogen in TMABHs has implication in designing volume efficient hydrides for hydrogen storage applications.