Characterization and photocatalytic activity of nitrogen-doped titanium(IV) oxide prepared by doping titania with TiN powder
详细信息    查看全文
文摘
Titanium(IV) oxide (TiO2) was doped with a small amount of TiN powder to obtain anatase nitrogen-doped TiO2(N-TiO2) with visible-light activity because the oxidation of TiN powder generally led to the formation of rutile N-doped TiO2. The synthesized N-TiO2 was yellow, and its UV-vis spectrum of N-TiO2 showed a continuous and tailing absorption in the visible region. The properties of N-TiO2 were compared with those of pureTiO2 and oxidized TiN particles. XRD patterns revealed that the ratio of the rutile phase to the anatase phase in N-TiO2 was lower than that in pure TiO2. These results indicate that the N atom dopants inhibit the phase transformation from anatase to rutile. The XRD patterns for all oxidized TiN particles showed the presence of the rutile phase. The results indicate that the TiO2 rutile phase is more likely to be formed by the heat treatment of TiN particles. The lack of phenol degradation in the presence of ST01 under visible light (423-600 nm) irradiation indicated that the TiO2 anatase phase was inactive to visible light. On the other hand, a decrease in the phenol content for N-TiO2 calcined at 600 ¡ãC (N-TiO2(600)), which was almost completely in the anatase form, revealed that N-doped anatase moieties responded favorably to visible light. The degradation amount for TiN particles oxidized at 600 ¡ãC (TiN(600)) was comparable to that for N-TiO2(600) in spite of the fact that the nitrogen content of TiN(600) was larger than that of N-TiO2(600) (N/Ti = 1.0 vs. N/Ti = 0.10, respectively). The low degradation amount of TiN(600) was most likely due to the low fraction of the anatase phase and the presence of the cubic TiN phase. N-TiO2 prepared using a small addition of TiN particles showed visible-light activity originating from the anatase N-doped moieties.

© 2004-2018 中国地质图书馆版权所有 京ICP备05064691号 京公网安备11010802017129号

地址:北京市海淀区学院路29号 邮编:100083

电话:办公室:(+86 10)66554848;文献借阅、咨询服务、科技查新:66554700