Abstract

• Novel Bi 2 S 3 /Bi 5 O 7 I porous hierarchical network-like Z-scheme heterojunctions with abundant OVs were prepared via an in-situ ion exchange etching method. • BSBI NHs were consisted of internal BiOI nanoplates and outside networks orderly interwoven by Bi 2 S 3 nanorods. • BSBI NHs displayed a significantly improved visible-light photocatalytic ability. • The construction of Z-scheme heterojunction and massive OVs resulted in the efficient separation of photogenerated charge carriers. • ∙OH, ⋅O 2 − and h + played primary roles during the photocatalytic process. In this study, a novel Bi 2 S 3 /BiOI Z-scheme photocatalyst with 3D porous hierarchical network-like heterostructure (BSBI NHs) and rich oxygen vacancies (OVs) was fabricated by a facile ion exchange method followed by the in-situ growth process. A possible formation mechanism of BSBI NHs was studied, showing the self-assembled process of in-situ interwoven growth of 1D Bi 2 S 3 nanorods (NRs) on the surface of 2D BiOI disk-like nanoplates (NPs), which followed the Ostwald ripening and epitaxial growth. The modification of BiOI NPs by Bi 2 S 3 NRs brought about the formation of Z-scheme heterojunction and massive OVs, which improved the visible-light response property and promoted the separation of photoexcited charge carriers of BSBI NHs. BSBI NHs exhibited a significantly enhanced photocatalytic activity compared with Bi 2 S 3 and BiOI, and BSBI-1 can remove almost all bacteria and Rhodamine B (RhB) after 60 min visible light illumination. In addition, the photocatalytic mechanism was studied and speculated based on the tests of active species capture, electron spin resonance (ESR), and density functional theory (DFT) simulation calculation, proving the primary roles of ∙OH, ·O 2 – , and h + during the photocatalytic reaction. This work provides new insights into the design and exploitation of novel heterojunctions with highly efficient photocatalytic performances for environmental remediation applications.

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