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In situ preparation of g-C3N4/Bi4O5I2 complex and its elevated photoactivity in Methyl Orange degradation under visible light.

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A graphite carbon nitride (g-C3N4) modified Bi4O5I2 composite was successfully prepared in-situ via the thermal treatment of a g-C3N4/BiOI precursor at 400°C for 3 hr. The as-prepared g-C3N4/Bi4O5I2 showed high photocatalytic… Click to show full abstract

A graphite carbon nitride (g-C3N4) modified Bi4O5I2 composite was successfully prepared in-situ via the thermal treatment of a g-C3N4/BiOI precursor at 400°C for 3 hr. The as-prepared g-C3N4/Bi4O5I2 showed high photocatalytic performance in Methyl Orange (MO) degradation under visible light. The best sample presented a degradation rate of 0.164 min-1, which is 3.2 and 82 times as high as that of Bi4O5I2 and g-C3N4, respectively. The g-C3N4/Bi4O5I2 was characterized by X-ray powder diffractometer (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), Raman, X-ray photoelectron spectroscopy (XPS), ultraviolet-visible diffuse reflectance spectra (DRS), electrochemical impedance spectroscopy (EIS) and transient photocurrent response in order to explain the enhanced photoactivity. Results indicated that the decoration with a small amount of g-C3N4 influenced the specific surface area only slightly. Nevertheless, the capability for absorbing visible light was improved measurably, which was beneficial to the MO degradation. On top of that, a strong interaction between g-C3N4 and Bi4O5I2 was detected. This interplay promoted the formation of a favorable heterojunction structure and thereby enhanced the charge separation. Thus, the g-C3N4/Bi4O5I2 composite presented greater charge separation efficiency and much better photocatalytic performance than Bi4O5I2. Additionally, g-C3N4/Bi4O5I2 also presented high stability. •O2- and holes were verified to be the main reactive species.

Keywords: c3n4; bi4o5i2; microscopy; spectroscopy; degradation; c3n4 bi4o5i2

Journal Title: Journal of environmental sciences
Year Published: 2020

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