摘要
The transition-metal dichalcogenides (TMDs) is a promising photocatalyst for degrading contaminant, while limited active sites and poor carrier mobility are the primary challenges for improving photocatalytic degrading efficiencies in both bare TMDs and TMDs-based photocatalysts. A rGO-MoSe 2 composite with 3D network hierarchical structure was fabricated by the GO-assisted solvothermal method. And then rGO-MoSe 2 /g-C 3 N 4 3D/2D hierarchical structures were constructed by combining rGO-MoSe 2 with g-C 3 N 4 nanosheets . The optimal rGO-MoSe 2 /g-C 3 N 4 composite exhibited the highest photocatalytic degrading rate of 97.4% towards RhB under simulated solar light, and its pseudo-first-order apparent rate constant ( k ) was 0.0715 min −1 , being 5.9 and 12.5-folds higher than that of MoSe 2 /g-C 3 N 4 (0.0121 min −1 ) and bare g-C 3 N 4 (0.00573 min −1 ), respectively. The 3D/2D hierarchical structure endow rGO-MoSe 2 /g-C 3 N 4 composite with the improved light-harvesting and abundant active sites, supported by the DRS and BET analyses. And rGO nanosheets could act as efficient transfer and separation channels for electron-hole pairs between MoSe 2 and g-C 3 N 4 , confirmed through the photocurrent response and EIS tests. According to the results of DRS spectra and Mott-Schottky plots, the spatial behavior of photo-induced carriers at interface of rGO-MoSe 2 /g-C 3 N 4 would comply to a Z-scheme transfer pathway under the synergy effects of the internal electric field and band bending.
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