4.8 Article

Inactive Cu2O Cubes Become Highly Photocatalytically Active with Ag2S Deposition

Journal

ACS APPLIED MATERIALS & INTERFACES
Volume 13, Issue 9, Pages 11515-11523

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acsami.1c00342

Keywords

charge transfer; cuprous oxide; facet-dependent properties; interfacial band alignment; photocatalysis

Funding

  1. Ministry of Science and Technology, Taiwan [MOST 107-2113-M-007-013-MY3, 109-2634-F-007-023, 109-2811-M-007-516]
  2. Ministry of Education, Taiwan

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By lightly depositing Ag2S nanoparticles on Cu2O cubes, significant photocatalytic activity was observed, supported by XRD and XPS analysis. The heterostructures showed enhanced activity, confirmed by EPR and photoluminescence measurements, indicating a potential Z-scheme charge transfer mechanism at the interface. Unexpectedly, separately synthesized Ag2S particles were found to be photocatalytically inactive.
Previously, Cu2O cubes have been shown to remain photocatalytically inert toward methyl orange degradation even after surface decoration with ZnO, ZnS, CdS, and Ag3PO4 nanostructures. Surprisingly, when Ag2S nanoparticles are lightly deposited on Cu2O cubes as seen through scanning electron microscopy (SEM) images, the heterostructures become highly photocatalytically active. X-ray diffraction (XRD) patterns show mainly Cu2O diffraction peaks due to lightly deposited Ag2S, but Ag2S peaks can emerge with increased Ag2S deposition. X-ray photoelectron spectroscopy (XPS) analysis also supports Ag2S formation on Cu2O crystals. The Ag2S-deposited Cu2O octahedra and rhombic dodecahedra show the expected activity enhancement. Electron paramagnetic resonance (EPR) measurements, as well as electron, hole, and radical scavenger tests, all confirmed the emergence of photocatalytic activity from the Ag2S-Cu2O cubes. Photoluminescence lifetimes are shortened after Ag2S deposition. Electrochemical impedance measurements revealed a large decrease in charge transfer resistance for Cu2O cubes after the Ag2S deposition. Unexpectedly, the separately synthesized Ag2S particles are also photocatalytically inactive. No specific lattice planes of Ag2S are formed directly over the {100} face of Cu2O. Diffuse reflectance and ultraviolet photoelectron spectral data were used to construct band diagrams of different Cu2O crystals and Ag2S nanoparticles. A Z-scheme charge transfer mechanism may be involved at the heterojunction interface to promote charge carrier separation. However, to explain the sudden appearance of photocatalytic activity from the Ag2S-deposited Cu2O cubes, a large change in the {100} surface band bending after Ag2S deposition should be used. This work illustrates that an unusual photocatalytic outcome is possible to semiconductor heterojunctions, where two photocatalytically inert components can become highly active when joined together.

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