Unveiling the activity origin of ultrathin BiOCl nanosheets for photocatalytic CO2 reduction

Ultrathin layered semiconductors have attracted particular attention for various photocatalytic applications, while their surface-structure changes under reaction conditions have been rarely concerned. Herein, the dynamic evolutions of surface atomic and electronic structures on ultrathin BiOCl photocatalysts were firstly explored by combining synchronous-illumination X-ray photoelectron spectroscopy (SI-XPS) with X-ray diffraction (SI-XRD). The related results clearly reveal that the exposed {001} facets of ultrathin BiOCl are terminated with chlorine atoms instead of generally considered oxygen atoms. Under steady states, the outward migration of chlorine atoms on BiOCl (001) surfaces resulted in the formation of Bi, Cl, and O atoms with multiple-valence states and length decrease of Cl-O and Bi-O bond within the lattice phase. Under excitation states, the surface chlorine atoms return back to the lattice phase, leading to the elongation of Bi-Cl and Bi-O bonds and the valence-state normalization of Bi, Cl, and O atoms. Owing to these significant atomic- and electronic-structure changes, ultrathin BiOCl nanosheets exhibit the prominent activity enhancement (21.4 mu mol g (-1) h (-1)) for CO2 reduction to CO compare with bulk BiOCl (3.3 mu mol g (-1) h (-1)).

Automated summary

This study investigated the dynamic changes in surface atomic and electronic structures of ultrathin BiOCl photocatalysts under reaction conditions, revealing the significant impact of exposed chlorine atoms on {001} facets. These structure changes resulted in a prominent enhancement in catalytic activity for CO2 reduction to CO in ultrathin nanosheets compared to bulk BiOCl.