We herein demonstrate self-doping of the CO 3 2− anionic group into a wide bandgap semiconductor Bi 2 O 2 CO 3 realized by a one-pot hydrothermal technique. The photoresponsive range of the self-doped Bi 2 O 2 CO 3 can be extended from UV to visible light and the band gap can be continuously tuned. Density functional theory (DFT) calculation results demonstrate that the foreign CO 3 2− ions are doped in the caves constructed by the four adjacent CO 3 2− ions and the CO 3 2− self-doping can effectively narrow the band gap of Bi 2 O 2 CO 3 by lowering the conduction band position and meanwhile generating impurity level. The photocatalytic performance is evaluated by monitoring NO removal from the gas phase, photodegradation of a colorless contaminant (bisphenol A, BPA) in an aqueous solution, and photocurrent generation. In comparison with the pristine Bi 2 O 2 CO 3 which is not sensitive to visible light, the self-doped Bi 2 O 2 CO 3 exhibits drastically enhanced visible-light photoreactivity, which is also superior to that of many other well-known photocatalysts such as P25, C 3 N 4 , and BiOBr. The highly enhanced photocatalytic performance is attributed to combination of both efficient visible light absorption and separation of photogenerated electron− hole pairs. The self-doped Bi 2 O 2 CO 3 also shows decent photochemical stability, which is of especial importance for its practical applications. This work demonstrates that self-doping with an anionic group enables the band gap engineering and the design of high-performance photocatalysts sensitive to visible light.
Non-centrosymmetric polar Bi2O2(OH)(NO3) with a rational band structure and {001} active exposing facets is developed as a robust layered photocatalyst for photooxidative diverse industrial contaminants and pharmaceuticals.
Solar-light driven CO2 reduction into value-added chemicals and fuels emerges as a significant approach for CO2 conversion. However, inefficient electron-hole separation and the complex multi-electrons transfer processes hamper the efficiency of CO2 photoreduction. Herein, we prepare ferroelectric Bi3TiNbO9 nanosheets and employ corona poling to strengthen their ferroelectric polarization to facilitate the bulk charge separation within Bi3TiNbO9 nanosheets. Furthermore, surface oxygen vacancies are introduced to extend the photo-absorption of the synthesized materials and also to promote the adsorption and activation of CO2 molecules on the catalysts’ surface. More importantly, the oxygen vacancies exert a pinning effect on ferroelectric domains that enables Bi3TiNbO9 nanosheets to maintain superb ferroelectric polarization, tackling above-mentioned key challenges in photocatalytic CO2 reduction. This work highlights the importance of ferroelectric properties and controlled surface defect engineering, and emphasizes the key roles of tuning bulk and surface properties in enhancing the CO2 photoreduction performance.
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