Supramolecular Immobilization of Laccase on Carbon Nanotube Electrodes Functionalized with (Methylpyrenylaminomethyl)anthraquinone for Direct Electron Reduction of Oxygen

An efficient way of immobilizing and wiring a large amount of laccase on non‐covalently‐functionalized multi‐walled carbon nanotube (MWCNT) electrodes is reported. 1‐(2‐anthraquinonylaminomethyl)pyrene and 1‐[bis(2‐anthraquinonyl)aminomethyl]pyrene were synthesized and studied for their capability to non‐covalently functionalize MWCNT electrodes and immobilize and orientate laccase on the nanostructured electrodes. This led to high‐performance biocathodes for oxygen reduction by direct electron transfer with maximum current densities of (1±0.2) mA cm^?2. The performance of the resulting bioelectrodes could be doubled simply by using the bis‐anthraquinone compound. The bioelectrodes show excellent stability over weeks and can thus be envisioned in enzymatic biofuel cells.