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Controllable Anchoring of Graphitic Carbon Nitride on MnO(2) Nanoarchitectures for Oxygen Evolution Electrocatalysis

[Image: see text] The design and fabrication of eco-friendly and cost-effective (photo)electrocatalysts for the oxygen evolution reaction (OER) is a key research goal for a proper management of water splitting to address the global energy crisis. In this work, we focus on the preparation of supporte...

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Detalles Bibliográficos
Autores principales: Benedet, Mattia, Gallo, Andrea, Maccato, Chiara, Rizzi, Gian Andrea, Barreca, Davide, Lebedev, Oleg I., Modin, Evgeny, McGlynn, Ruairi, Mariotti, Davide, Gasparotto, Alberto
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2023
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10571007/
https://www.ncbi.nlm.nih.gov/pubmed/37769189
http://dx.doi.org/10.1021/acsami.3c09363
Descripción
Sumario:[Image: see text] The design and fabrication of eco-friendly and cost-effective (photo)electrocatalysts for the oxygen evolution reaction (OER) is a key research goal for a proper management of water splitting to address the global energy crisis. In this work, we focus on the preparation of supported MnO(2)/graphitic carbon nitride (g-CN) OER (photo)electrocatalysts by means of a novel preparation strategy. The proposed route consists of the plasma enhanced-chemical vapor deposition (PE-CVD) of MnO(2) nanoarchitectures on porous Ni scaffolds, the anchoring of controllable g-CN amounts by an amenable electrophoretic deposition (EPD) process, and the ultimate thermal treatment in air. The inherent method versatility and flexibility afforded defective MnO(2)/g-CN nanoarchitectures, featuring a g-CN content and nano-organization tunable as a function of EPD duration and the used carbon nitride precursor. Such a modulation had a direct influence on OER functional performances, which, for the best composite system, corresponded to an overpotential of 430 mV at 10 mA/cm(2), a Tafel slope of ≈70 mV/dec, and a turnover frequency of 6.52 × 10(–3) s(–1), accompanied by a very good time stability. The present outcomes, comparing favorably with previous results on analogous systems, were rationalized on the basis of the formation of type-II MnO(2)/g-CN heterojunctions, and yield valuable insights into this class of green (photo)electrocatalysts for end uses in solar-to-fuel conversion and water treatment.