Polyaniline-Pyrrole Electronic Interaction as a Potential Cathode Modifier in Magnesium-Sulfur Battery: An Ab Initio Study

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Abstract

Magnesium-sulfur (Mg-S) batteries present a compelling energy storage solution, characterised by their remarkable theoretical energy density and economic viability. Nonetheless, challenges arise, including swift capacity degradation and suboptimal polysulfide (acting as an electronic and ionic insulator) utilisation, mainly due to a phenomenon known as the polysulfide "shuttle effect". This effect also leads to a decline in battery performance. The B3LYP functional and 6-311G (d, p) basis set were used to examine the optoelectronic and charge-transfer properties of a polyaniline-pyrrole (PANIPyr) composite, emphasising interatomic and electronic interactions that enhance charge transport and oxidation of MgS₂. The findings demonstrate the presence of coordination bonding between hydrogen in pyrrole and the N- ion in quinonediimine of polyaniline, significantly enhancing the electrical properties of PANI. The PANIPyr_P1 configuration exhibits the lowest Ɛgap and the highest charge-transfer capacity, thereby improving reactivity towards polysulfides in comparison to pure PANI. Significant electrical interactions at this site establish accessible electrophilic and nucleophilic regions that stabilise the ionic sides of the polysulfides, reduce the shuttle effect, and improve charge transport at the interface. PANIPyr_P1 demonstrates viability for minimising polysulfide migration and enhancing cathodic efficiency in Mg-S batteries, thereby laying a foundation for future investigations into polymer-based cathode modifiers.

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