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Strengthening the separation of photogenerated charge carriers is crucial for improving the efficiency of photocatalytic hydrogen evolution. Herein, t-Mn0.5Cd0.5S/Ov-WO3 (t-MCSW) triple-phase junctions with rich oxygen vacancies were developed using the calcination-hydrothermal method. The corresponding morphology and structure of the samples were examined by XRD, TEM and XPS. The formation of the S-scheme heterostructure in t-MCSW has also been confirmed with in situ XPS, work function analysis and free radical capture tests. The experimental results demonstrate that t-MCSW-7 exhibited optimal activity (194.2 mmol g−1 h−1), which was about 4 times higher than that of the individual Mn0.5Cd0.5S (t-MCS, 48.8 mmol g−1 h−1). The apparent quantum yield of t-MCSW-7 is 29.14% at 420 nm, and the material exhibits excellent stability after seven cycles of photocatalytic reaction. The excellent photocatalytic activity of t-MCSW-7 is attributed to more efficient separation of charge carriers by triple-phase junctions connected by homojunctions and heterojunctions. Moreover, the existence of oxygen vacancies broadens absorption spectra and accelerates surface charge transfer. The synergistic effect of phase junctions and oxygen vacancies leads to an enhancement of hydrogen evolution activity. This work provides a new idea for preparing efficient photocatalysts. [ABSTRACT FROM AUTHOR]

Herein we have demonstrated the synthesis of nitrogen vacancy enriched exfoliated B-doped g-C3N4 (e-BCN) through a facile thermal exfoliation method, characterized it using different analytical techniques and compared its photocatalytic activity with that of bulk B-doped g-C3N4 (BCN). The decrease in peak intensity and slight shift of the 2 value in the PXRD patterns confirmed the successful exfoliation of bulk BCN to an e-BCN nanosheet. FESEM and HRTEM images also indicated the formation of a thin layered nanosheet of e-BCN as compared to bulk BCN. The PL and EIS data suggested the reduced recombination rate and superior separation capability of the photo-generated charge carriers of e-BCN. The introduction of nitrogen vacancies on the surface of e-BCN is confirmed by the FTIR and XPS analyses. The increased photocurrent density of 524 μA cm−2 displayed by e-BCN indicated the better availability of photo-generated electrons due to the higher separation of charge carriers than in the bulk BCN. The as-prepared e-BCN nanosheet exhibited enhanced photocatalytic performance 1.2 and 3.7 fold greater than that of bulk BCN towards ciprofloxacin degradation and H2 generation, respectively, under visible light irradiation. The excellent photocatalytic behavior of e-BCN was ascribed to the augmented active sites with reduced recombination efficiency and increased separation ability of the photo-induced e−/h+ pairs of the e-BCN nanosheet. This work suggested the facile fabrication of e-BCN through the thermal exfoliation process and its photocatalytic activity towards pollutant degradation and hydrogen evolution. [ABSTRACT FROM AUTHOR]