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Carbon Dot-Doped Titanium Dioxide Sheets for the Efficient Photocatalytic Performance of Refractory Pollutants.

ABSTRACT: Broad solar light harvesting and fast photoinduced electron-hole migration are two critical factors for the catalytic capacity of photocatalytic system. In this study, novel visible light-driven carbon dot-TiO₂ nanosheet (CD-TN) photocatalysts are successfully prepared by loading CDs on the surface of TNs through the hydrothermal method. The microstructure, chemical components, and optical properties of the prepared samples are characterized via X-ray diffraction, Fourier transform infrared spectroscopy, transmission electron microscopy, UV-visible diffuse reflectance spectroscopy, and X-ray photoelectron spectroscopy analysis. Congo red (CR), rhodamine B (RhB), and tetracycline (TC) are selected as pollutants to assess the catalytic performance of CD-TNs. As expected, the removal efficiencies of CD-TNs for CR, RhB, and TC are 94.6% (120 min), 97.2% (150 min), and 96.1% (60 min), respectively, obviously higher than that of pure TNs. The enhanced degradation efficiency of CD-TNs is predominantly ascribed to the merits of CDs (excellent up-conversion property and electron transfer property). Moreover, according to the several degradation cycles, CD-TNs possess the excellent stability, having removed 93.3% of CR after 120 min irradiation.

SUBMITTER: Shen S

PROVIDER: S-EPMC8453265 | biostudies-literature |

REPOSITORIES: biostudies-literature

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Project description:Metal-doped graphitic carbon nitride (MCN) materials have shown great promise as effective photocatalysts for the conversion of acetic acid to carbon dioxide under UV-visible irradiation and are superior to pristine carbon nitride (g-C3N4 , CN). In this study, the effects of metal dopants on the physicochemical properties of metal-doped CN samples (Fe-, Cu-, Zn-, FeCu-, FeZn-, and CuZn-doped CN) and their catalytic activity in the photooxidation of acetic acid were investigated and discussed for their correlation, especially on their surface and bulk structures. The materials in the order of highest to lowest photocatalytic activity are FeZn_CN, FeCu_CN, Fe_CN, and Cu_CN (rates of CO2 evolution higher than for CN), followed by Zn_CN, CuZn_CN, and CN (rates of CO2 evolution lower than CN). Although Fe doping resulted in the extension of the light absorption range, incorporation of metals did not significantly alter the crystalline phase, morphology, and specific surface area of the CN materials. However, the extension of light absorption into the visible region on Fe doping did not provide a suitable explanation for the increase in photocatalytic efficiency. To further understand this issue, the materials were analyzed using two complementary techniques, reversed double-beam photoacoustic spectroscopy (RDB-PAS) and electron spin resonance spectroscopy (ESR). The FeZn_CN, with the highest electron trap density between 2.95 and 3.00 eV, afforded the highest rate of CO2 evolution from acetic acid photodecomposition. All Fe-incorporated CN materials and Cu-CN reported herein can be categorized as high activity catalysts according to the rates of CO2 evolution obtained, higher than 0.15 μmol/min-1, or >1.5 times higher than that of pristine CN. Results from this research are suggestive of a correlation between the rate of CO2 evolution via photocatalytic oxidation of acetic acid with the threshold number of free unpaired electrons in CN-based materials and high electron trap density (between 2.95 and 3.00 eV).

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Carbon Dot-Doped Titanium Dioxide Sheets for the Efficient Photocatalytic Performance of Refractory Pollutants.

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