Unraveling Synergistic Redox Interactions in Tetraphenylporphyrin-Polyluminol-Carbon Nanotube Composite for Capacitive Charge Storage.

Organic redox-active materials, combined with high-surface-area carbonaceous substrates, form sustainable and low-cost composites with greatly enhanced electrochemical charge storage capacities. The electrochemical capacitive behavior of a composite electrode containing tetraphenylporphyrin sulfonate (TPPS), Chemically polymerized luminol (CpLum), and carbon nanotubes (TPPS-CpLum-CNT) was studied and compared with individual TPPS-CNT and CpLum-CNT composites. The dual-layer TPPS-CpLum had a combined contribution to the electrochemical charge storage, which led to an increased volumetric capacitance over the bare CNT and individual TPPS-CNT and CpLum-CNT composites. The synergistic interactions in the composite enabled faster charge storage kinetics and great stability. Spectroscopic analyses revealed that TPPS and CpLum interact electronically through noncovalent π-π and van der Waals bonds, which facilitates the transfer of electrons during charge and discharge. The synergy in charge storage was confirmed by density functional theory computational analysis, which suggested favorable physisorption and interfacial electronic interactions for TPPS adsorbed to a CpLum-carbon substrate. The combined insights from experimental and computational characterizations show that superimposing redox-active organic layers can be an effective and sustainable approach to design and engineer the surface of carbonaceous materials for capacitive charge storage.