摘要
A visible-light-driven photoelectrochemical (PEC) sensor has been developed for probing Hg 2+ with “turn-on” signal output using hollow CoS x @CdS polyhedron as direct Z-scheme photocatalyst and Hg 2+ -recognition probe. The CoS x @CdS heterojunction photocatalysts were fabricated by growing CdS nanoparticles on the surface of cobalt sulfide (CoS x ) 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 CoS x @CdS-modified ITO electrodes could be specifically turned on by Hg 2+ , in contrast to these of the CoS x or CdS-modified ones showing no significant Hg 2+ -induced photocurrent. Under visible light irradiation, herein, the synergetic combination of CoS x 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 Hg 2+ through the selective ion-exchange reaction to trigger the in-situ formation of a new Z-scheme heterojunction of CoS x @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 Hg 2+ 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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