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Facile Functionalization of Carbon Electrodes for Efficient Electroenzymatic Hydrogen Production

Yongpeng Liu, Sophie Webb, Pavel Moreno‐García, Amogh Kulkarni, Plinio Maroni, Peter Broekmann, Ross D. Milton

2023JACS Au20 citationsDOIOpen Access PDF

Abstract

High Resolution Image Download MS PowerPoint Slide Enzymatic electrocatalysis holds promise for new biotechnological approaches to produce chemical commodities such as molecular hydrogen (H 2 ). However, typical inhibitory limitations include low stability and/or low electrocatalytic currents (low product yields). Here we report a facile single-step electrode preparation procedure using indium–tin oxide nanoparticles on carbon electrodes. The subsequent immobilization of a model [FeFe]-hydrogenase from Clostridium pasteurianum (“CpI”) on the functionalized carbon electrode permits comparatively large quantities of H 2 to be produced in a stable manner. Specifically, we observe current densities of >8 mA/cm 2 at −0.8 V vs the standard hydrogen electrode (SHE) by direct electron transfer (DET) from cyclic voltammetry, with an onset potential for H 2 production close to its standard potential at pH 7 (approximately −0.4 V vs. SHE). Importantly, hydrogenase-modified electrodes show high stability retaining ∼92% of their electrocatalytic current after 120 h of continuous potentiostatic H 2 production at −0.6 V vs. SHE; gas chromatography confirmed ∼100% Faradaic efficiency. As the bioelectrode preparation method balances simplicity, performance, and stability, it paves the way for DET on other electroenzymatic reactions as well as semiartificial photosynthesis.

Topics & Concepts

HydrogenaseElectrocatalystElectrodeCyclic voltammetryChemistryIndium tin oxideFaraday efficiencyHydrogen productionCarbon fibersHydrogenInorganic chemistryMaterials scienceChemical engineeringElectrochemistryOrganic chemistryPhysical chemistryComposite materialComposite numberEngineeringElectrocatalysts for Energy ConversionAdvanced battery technologies researchMetalloenzymes and iron-sulfur proteins