Tungsten Disulfide-Interfacing Nickel-Porphyrin For Photo-Enhanced Electrocatalytic Water Oxidation

Covalent functionalization of tungsten disulfide (WS2) with photo- and electro-active nickel-porphyrin (NiP) is reported. Exfoliated WS2 interfacing NiP moieties with 1,2-dithiolane linkages is assayed in the oxygen evolution reaction under both dark and illuminated conditions. The hybrid material presented, WS2-NiP, is fully characterized with complementary spectroscopic, microscopic, and thermal techniques. Standard yet advanced electrochemical techniques, such as linear sweep voltammetry, electrochemical impedance spectroscopy, and calculation of the electrochemically active surface area, are used to delineate the catalytic profile of WS2-NiP. In-depth study of thin films with transient photocurrent and photovoltage response assays uncovers photo-enhanced electrocatalytic behavior. The observed photo-enhanced electrocatalytic activity of WS2-NiP is attributed to the presence of Ni centers coordinated and stabilized by the N-4 motifs of tetrapyrrole rings at the tethered porphyrin derivative chains, which work as photoreceptors. This pioneering work opens wide routes for water oxidation, further contributing to the development of non-noble metal electrocatalysts.

Automated summary

This study reports on the covalent functionalization of tungsten disulfide (WS2) with photo- and electro-active nickel-porphyrin (NiP). The hybrid material WS2-NiP is characterized using spectroscopic, microscopic, and thermal techniques, and evaluated for its electrocatalytic behavior using advanced electrochemical techniques. The observed photo-enhanced electrocatalytic activity is attributed to the presence of Ni centers coordinated by tethered porphyrin derivative chains, which serve as photoreceptors. This pioneering work opens up new possibilities for water oxidation and the development of non-noble metal electrocatalysts.