4.6 Article

Hierarchically Grown CaMn3O6 Nanorods by RF Magnetron Sputtering for Enhanced Visible-Light-Driven Photocatalysis

Journal

JOURNAL OF PHYSICAL CHEMISTRY C
Volume 118, Issue 41, Pages 24127-24135

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/jp507070u

Keywords

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Funding

  1. FEDER, through Programa Operacional Factores de Competitividade COMPETE and Fundacao para a Ciencia e a Tecnologia FCT [PTDC/AAC-AMB/103112/2008]
  2. FCT [PEst-OE/QUI/UI0612/2013, PEst-OE/FIS/UI0068/2011]
  3. Fundação para a Ciência e a Tecnologia [PTDC/AAC-AMB/103112/2008] Funding Source: FCT

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CaMn3O6 films with hierarchical nanostructures were deposited for the first time on unheated quartz glass substrates by the radio frequency (RF) magnetron sputtering technique using a polycrystalline CaMnO3 sample as sputtering target, and their photocatalytic activity was evaluated on the decolorization of Rhodamine 6G (Rh6G) aqueous solutions. The films scanning electron microscope (SEM) images evidence a growth of nanorods (NRs) arrays with planar endings and a narrow size distribution centered at about 30 nm in diameter. The CaMn3O6 films surface is uniform and presents a high density of nanorods (116 nanorods per um(2)). The high surface area combined with the tunnels crystallographic structure, evidenced by X-ray diffraction (XRD), results in an effective photocatalyst for Rh6G degradation under visible light irradiation. Based on the photodegradation experiments, it is suggested that a process of dye self-sensitization can be one of the key factors of the superior photocatalytic performance of CaMn3O6 NRs. The kinetics of photocatalytic degradation of Rh6G follows a first-order reaction. Furthermore, XRD of the used films did not reveal additional phases indicating high photochemical stability, and the diffuse reflection infrared Fourier transform spectrum (DRIFT) does not show adsorbed organic species on the CaMn3O6 NRs surface. This work provides a potential route to develop high-performance immobilized nanostructures, and the achievements open up many possibilities to tailor visible light active materials for environmental applications.

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