Hydrogen atom/molecule adsorption on 2D metallic porphyrin: A first-principles study

TL;DR

This study uses first-principles DFT simulations to analyze hydrogen adsorption mechanisms on 2D metallic porphyrins with transition metals, revealing chemisorption and physisorption behaviors relevant for hydrogen storage.

Contribution

It provides detailed insights into the adsorption energies, charge transfer, and effects of strain on hydrogen interaction with 2D metallic porphyrins, advancing understanding for energy storage applications.

Findings

Chemsorption of atomic hydrogen with maximum energy -3.7 eV on V or Cr porphyrins.

Physisorption of molecular hydrogen with maximum energy -122.5 meV on Sc porphyrins.

Uniaxial strain has minimal impact on adsorption properties.

Abstract

Hydrogen is a promising element for applications in new energy sources like fuel cells. One key issue for such applications is storing hydrogen. And, to improve storage capacity, understanding the interaction mechanism between hydrogen and possible storage materials is critical. This work uses DFT simulations to comprehensively investigate the adsorption mechanism of H/H$_2$ on the 2D metallic porphyrins with one transition metal in its center. Our results suggest that the mechanism for adsorption of H (H$_2$) is chemisorption (physisorption). The maximum adsorption energy for atomic hydrogen was $-3.7$ eV for 2D porphyrins embedded with vanadium or chromium atoms. Our results also revealed charge transfer of up $-0.43$ e to chemisorbed H atoms. In contrast, the maximum adsorption energy calculated for molecular hydrogen was $-122.5$ meV for 2D porphyrins embedded with scandium atoms. Furthermore, charge transfer was minimal for physisorption. Finally, we also determined that uniaxial strain has a minimal effect on the adsorption properties of 2D metallic porphyrins.