Cobalt porphyrin/molybdenum disulfide nanoensembles for light-assisted electrocatalytic water oxidation and selective hydrogen peroxide production

The development of photo/electroactive catalysts sustainably producing hydrogen from water splitting and selectively hydrogen peroxide is of paramount importance to alleviate climate change effects. Herein, an anionic cobalt porphyrin (CoP) derivative is electrostatically interfaced with a positivel...

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Veröffentlicht in:2d materials 2023-01, Vol.10 (1), p.14007
Hauptverfasser: Perivoliotis, Dimitrios K, Stangel, Christina, Sato, Yuta, Suenaga, Kazu, Tagmatarchis, Nikos
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Sprache:eng
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Zusammenfassung:The development of photo/electroactive catalysts sustainably producing hydrogen from water splitting and selectively hydrogen peroxide is of paramount importance to alleviate climate change effects. Herein, an anionic cobalt porphyrin (CoP) derivative is electrostatically interfaced with a positively charged modified molybdenum disulfide (MoS 2 ), forming CoP/MoS 2 , which is accordingly employed as nonprecious photo/electrocatalyst for water oxidation reaction (WOR) and selective H 2 O 2 production. According to the results, CoP/MoS 2 shows remarkable bifunctional photo/electrocatalytic performance for WOR and 2e − pathway O 2 reduction reaction (ORR) in alkaline electrolyte. Upon visible light irradiation, electrochemical measurements on a fluorine-doped tin oxide (FTO) coated glass electrode reveal an onset potential of 0.595 mV (ORR) and 1.575 mV (WOR) vs. reversible hydrogen electrode, being improved by approximately 80 mV, in both cases, compared to the dark conditions. Notably, the use of the FTO set-up not only enabled us to evaluate the photo/electrocatalytic activity of the CoP/MoS 2 nanoensemble but also mimics the practical conditions in photo/electrochemical devices. The outstanding bifunctional photo/electrocatalytic performance of CoP/MoS 2 is attributed to (a) the use of CoP as versatile single-atom molecular catalyst and photosensitizer (b) the strong ion-pair interactions between cationic modified MoS 2 and the anionic CoP derivative, which prevent aggregation, ensuring better accessibility of the reactants to cobalt active sites, and (c) the co-existence of 1T and 2H phase at modified MoS 2 , offering improved electrical conductivity and intrinsic electrocatalytic activity along with enhanced intraensemble electronic interactions upon illumination. This work is expected to inspire the design of advanced and low-cost materials for the sustainable production of renewable fuels.
ISSN:2053-1583
2211-3398
2053-1583
2211-3398
DOI:10.1088/2053-1583/ac9290