Abstract

A visible-light-driven photoelectrochemical (PEC) sensor has been developed for probing Hg2+ with “turn-on” signal output using hollow CoSx@CdS polyhedron as direct Z-scheme photocatalyst and Hg2+-recognition probe. The CoSx@CdS heterojunction photocatalysts were fabricated by growing CdS nanoparticles on the surface of cobalt sulfide (CoSx) via one-pot solvothermal route using metal-organic frameworks (MOFs) of ZIF-67 polyhedrons as the sacrificial templates and cobalt precursors. It was discovered that the photocurrent responses of the CoSx@CdS-modified ITO electrodes could be specifically turned on by Hg2+, in contrast to these of the CoSx or CdS-modified ones showing no significant Hg2+-induced photocurrent. Under visible light irradiation, herein, the synergetic combination of CoSx and CdS components could improve the carriers transferring of PEC system. More importantly, the photocurrents of the PEC sensor could be greatly enhanced in the presence of Hg2+ through the selective ion-exchange reaction to trigger the in-situ formation of a new Z-scheme heterojunction of CoSx@CdS/HgS photocatalysts, achieving the further promoted charge transferring and suppressed recombination of photogenerated electron-hole pairs. The developed double heterojunctions-based PEC sensors can detect Hg2+ with the concentrations ranging from 0.010 to 1000 nM, which performances are much better than those of the current PEC analysis methods. Besides, such a MOF-templated one-pot construction route may pave the way toward the design of various direct Z-scheme heterojunction photocatalysts of PEC probes of great interest.

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