摘要
An ordered 1T/2H MoSe 2 possessed few-layers nanosheets structure was synthesized by a NaBH 4 -assisted hydrothermal method. Further, 1T/2H MoSe 2 was integrated with proton g-C 3 N 4 via solvothermal method, forming a novel 2D/2D heterostructure composite (1T/2H MoSe 2 /pg-C 3 N 4 ) with Z-scheme heterojunction. 1T/2H MoSe 2 /pg-C 3 N 4 had narrower bandgap, abundant active sites, as well as better photocurrent response and conductivity, confirmed by spectroscopic and electrochemical characterizations. Consequently, the optimal 1T/2H MoSe 2 /pg-C 3 N 4 at 1 wt% MoSe 2 loading showed enhanced TC (RhB) photodegrading rate of 92% (99%), within 80 min (45 min) of simulated solar light irradiation, being 3.0 (3.4) and 1.2 (1.2) times than that of pg-C 3 N 4 and 2H MoSe 2 /pg-C 3 N 4 , respectively. Additionally, active species trapping experiments indicated that O 2 − and h + were the main species of contaminants degradation over 1T/2H MoSe 2 /pg-C 3 N 4 . Combining with DRS, Mott-Schottky and VB XPS analysis, a reasonable 1T phase boosted Z-scheme MoSe 2 -based heterojunction mechanism was proposed.
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