摘要
Photocatalytic denitrification has attracted great attention owing to its high efficiency and environmentally friendly features. However, selectively photocatalytic reduction of high concentration nitrate to N 2 is still a challenging problem due to the competition of photons between nitrate and photocatalysts. Herein, the Ag/SiO 2 core encapsulated in the crystalline TiO 2 shell (Ag/SiO 2 @ c TiO 2 ) was constructed for improvement of photocatalytic denitrification. Finite difference time domain (FDTD) simulation demonstrated that strong light scattering improved light harvesting via optical confinement. Meanwhile, surface plasmon resonance and electron sink effect of Ag not only enhanced the photogenerated electrons density but also promoted charge carriers separation of Ag/SiO 2 @ c TiO 2 . More importantly, e cb − of TiO 2 -shell could be immediately transferred to Ag to keep the balance between Ag 0 and Ag + , which contributed to the good stability of Ag/SiO 2 @ c TiO 2 . 95.8% nitrate ( C 0 = 2000 mg/L) was removed by 5 wt%Ag/SiO 2 @ c TiO 2 with N 2 selectivity of 93.6% within 4 h. Even after five cycles, 5 wt%Ag/SiO 2 @ c TiO 2 still remained high photocatalytic denitrification efficiency (92.2%). Notably, since TiO 2 -shell prevented the reaction between Ag and Cl − , more than 92% nitrate could be removed within 5.3 h in the presence of high concentration Cl − .
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