Surface modification boosts exciton extraction in confined layered structure for selective oxidation reaction

Extracting photogenerated species from bulk to surface is an essential process for gaining efficient semiconductor-based photocatalysis. However, compared with charged photogenerated carriers, neutral exciton exhibits negligible response to electric field. Accordingly, traditional strategies involving band-alignment construction for boosting directional transfer of charge carriers are impracticable for extracting bulk excitons. To this issue, we here propose that the extraction of bulk exciton could be effectively implemented by surface modification. By taking confined layered bismuth oxycarbonate (Bi2O2CO3) as an example, we highlight that the incorporation of iodine atoms on the surface could modify the micro-region electronic structure and hence lead to reduced energy of surface excitonic states. Benefiting from the energy gradient between bulk and surface excitonic states, iodine-modified Bi2O2CO3 possesses high-efficiency bulk exciton extraction, and hence exhibits promoted performance in triggering O-1(2)-mediated selective oxidation reaction. This work presents the positive role of surface modification in regulating excitonic processes of semiconductor-based photocatalysts.

Automated summary

This study proposes the effective extraction of bulk excitons in semiconductor photocatalysts through surface modification, lowering the energy of surface excitonic states by altering the electronic structure. This process creates a high-efficiency extraction of bulk excitons, leading to improved performance in triggering selective oxidation reactions through O-1(2) mediation.