Abstract

Semiconductor driven photocatalysis has been demonstrated to be one of the promising and effective approaches to resolve the increasing energy and environmental crises by utilizing solar energy. As a typical metal-free semiconductor photocatalyst, graphitic carbon nitride (g-C3N4) has attracted tremendous attention in the photocatalytic water splitting, CO2 reduction and organic pollutants degradation. Unfortunately, the rapid recombination of photoinduced electron-hole pairs of g-C3N4 severely restrained its photocatalytic performance. To this end, lanthanum manganate (LaMnO3) was used to interact with g-C3N4 to rationally construct a direct Z-scheme LaMnO3/g-C3N4 hybrid as an efficient visible-light-driven photocatalyst for the photocatalytic degradation of tetracycline (TC). As expected, the LaMnO3/g-C3N4 product exhibited significant improvement on the performance of photocatalytic TC degradation in aqueous solution under visible light irradiation (λ > 420 nm). Especially, the optimized LaMnO3(9.8 wt%)/g-C3N4 hybrid with 9.8 wt% LaMnO3 achieved the highest apparent first-order rate constant, which was around 10.6 times larger than that of pristine g-C3N4 and 4.0 times greater than that of single LaMnO3. Such an enhanced photocatalytic activity could be ascribed to the formation of unique Z-scheme LaMnO3/g-C3N4 feature, which not just efficiently promoted the separation of the photoinduced electron-hole pairs, but also maintained the strong reducibility of electrons in the conduction band of g-C3N4 and high oxidizability of holes in the valence band of LaMnO3. Furthermore, a probable degradation mechanism was tentatively proposed based on the results of energy band structures, active species trapping experiments, photoluminescence spectroscopy and photoelectrochemical measurements. This work creates a new opportunity for the rational design and construction of highly efficient and stable g-C3N4-based Z-scheme hybrid photocatalysts for applying in environmental remediation and energy conversion.

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