摘要
Visible-light-driven and ultra-stable CoS x /CdS photocatalysts were controllably fabricated by the ZIF-67-templated one-pot solvothermal route for highly efficient photocatalytic Cr(VI) reduction. It was discovered that the resulting CoS x /CdS composites could present different photocatalytic activities controllably depending on the CoS x -to-CdS molar ratios used. The one with 1/16 M ratio could display the highest photocatalytic reduction performance for Cr(VI) with the efficiency up to 100% within 30 min, which is 5.6-fold and 2.1-fold higher than that of pristine CoS x and CdS, respectively. Herein, the components of CoS x and CdS with well-matched energy-band structures might serve separately as the electrons donor and the holes quencher to prolong the lifetime of photogenerated electrons in CoS x /CdS composites. A direct Z-scheme heterojunction could be thus constructed for promoting the charge carrier transferring with the improved redox abilities, leading to the robust photocatalysis of CoS x /CdS photocatalyst. Moreover, the developed CoS x /CdS photocatalyst could present superior stability with the structure and activity well survived after five photocatalytic cycles. This work may pave the way towards the controllable construction of a direct Z-scheme photocatalytic system by synergistically combining two kinds of components with matched energy-band structures, achieving the enhanced photocatalysis for the wide applications in the environmental remediation field.
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