Stabilize the oxygen vacancies in Bi2SiO5 for durable photocatalysis via altering local electronic structure with phosphate dopant

Oxygen vacancies in catalysts can bring new properties, especially the enhanced catalytic efficiencies that are absent in their pristine counterparts. However, the deactivation of oxygen vacancies inevitably limits the durability of catalytic performance. Herein, a model of photocatalytic NO oxidation over Bi2SiO5 catalyst is selected to unravel the pivotal role of dopants in enhancing the long-term stability of oxygen vacancies. The introduction of phosphate dopants could stabilize oxygen vacancies via turning the local electronic structure. The phosphate dopants evoke the enhanced electron redistribution and cause the charge compensation to unsatu-rated coordination atoms around the oxygen vacancies. The unique electronic structure modulated by dopants could facilitate the adsorption and activation of H2O and O2, impeding those atoms from filling into oxygen vacancies. This work provides an innovative route for rationally altering the local electronic structure of catalysts toward efficient and sustainable photocatalytic applications.

Automated summary

This study focuses on the role of dopants in enhancing the long-term stability of oxygen vacancies in a photocatalytic NO oxidation model over Bi2SiO5 catalyst. The introduction of phosphate dopants stabilizes oxygen vacancies by altering the local electronic structure, leading to enhanced electron redistribution and charge compensation to the unsaturated coordination atoms surrounding the vacancies. The unique electronic structure modulated by dopants facilitates the adsorption and activation of H2O and O2, preventing the filling of these atoms into the vacancies.