First-principle computational insights on Furan- and Thiophene- functionalized zinc-porphyrins as high performance organic cathodes for electrochemical energy storage systems

Organic electrode materials (OEMs) are increasingly replacing conventional inorganic counterparts in metal ion batteries (MIBs) due to their cost-effectiveness and environmental compatibility. Porphyrin-based materials, particularly metalloporphyrins (M-Porph), have garnered significant attention for electrochemical energy storage systems (EESS) owing to their bipolar electrochemical reactivity, making them suitable as both cathodic and anodic materials. However, the correlation between their structure and performance needs further exploration. This computational study examines the redox properties, thermodynamics, and theoretical performance of Zinc(II)-Porphyrin (Zn-Porph) with furan and thiophene substituents. The redox potential (E°) of Zn-Porph changes by 0.17 V with thiophene substituents instead of furan. Thiophene stabilizes the LUMO by 0.105 eV, indicating enhanced electron affinity and faster electron-accepting processes, while the HOMO shows a 0.085 eV stabilization. Thermodynamic calculations reveal that the reduction process intermediates for Zinc(II)-thiophene-Porph are less stable (ΔΔG° = 0.12 eV) than those for furan, suggesting a more accelerated electrochemical process. Additionally, density of states (DOS) analysis of Zn-T18 shows a non-zero DOS at the Fermi energy, indicating available electronic states for occupancy and highlighting its conductive properties. Upon complexation with PF6¯, the Fermi level shifts, reflecting electronic state redistribution and stabilization. The oxidized form, Zn-T16, retains a non-zero DOS at the Fermi energy despite significant Fermi level shifts, ensuring continued electronic conductivity. These findings underscore the robustness and versatility of Zn-porphyrin cathodes in EESS, demonstrating their potential to meet the demands for efficient, cost-effective, and environmentally friendly energy storage solutions.

Other Information

Published in: Electrochimica Acta
License: http://creativecommons.org/licenses/by/4.0/
See article on publisher's website: https://dx.doi.org/10.1016/j.electacta.2024.145234