Department of Environmental Engineering, Kyungpook National University, Daegu 702-701, Republic of Korea.
Department of Environmental Engineering, Kyungpook National University, Daegu 702-701, Republic of Korea.
J Hazard Mater. 2016 Aug 15;314:22-31. doi: 10.1016/j.jhazmat.2016.04.012. Epub 2016 Apr 8.
Two-dimensional nanosheet structures of N-doped TiO2/WO3 composites (WO3-N-TNSs) with varying WO3 loadings were synthesized by incorporating WO3 and N sources into sonochemically prepared TiO2 nanosheets (TNSs). These nanostructures were employed as photocatalysts, and their efficacy in the decomposition of hazardous hexane vapor was investigated. The photocatalytic efficiencies of the WO3-N-TNS composites were higher than those of N-doped TNS (N-TNS), which in turn were higher than the corresponding values for un-doped TNS. These variations were ascribed to the different light absorbance efficiencies, adsorption abilities, and charge carrier separations between the samples. An optimal WO3 loading for the performance of WO3-N-TNS was determined. Interestingly, the photocatalytic efficiency for hexane mixed with isopropyl alcohol (IPA) was lower than that for pure hexane, whereas the degradation efficiency for IPA did not vary with the feed method. Also investigated were the hexane conversion into CO2 over a representative WO3-N-TNS sample, the durability of the photocatalyst, and potential byproduct formation. Based on measurements of the hydroxyl radical population, a heterojunction-type mechanism was considered more plausible than a direct Z-scheme-type mechanism for the photocatalytic decomposition of hexane over the WO3-N-TNS photocatalysts.
采用超声法将 WO3 和 N 源掺入 TiO2 纳米片中制备了 N 掺杂 TiO2/WO3 复合材料(WO3-N-TNS)的二维纳米片结构,其 WO3 负载量不同。这些纳米结构被用作光催化剂,研究了它们在分解有害的正己烷蒸气方面的效果。WO3-N-TNS 复合材料的光催化效率高于 N 掺杂的 TNS(N-TNS),而 N-TNS 的效率又高于未掺杂的 TNS。这些变化归因于不同的光吸收效率、吸附能力和样品之间的载流子分离。确定了 WO3-N-TNS 性能的最佳 WO3 负载量。有趣的是,正己烷与异丙醇(IPA)的混合的光催化效率低于纯正己烷,而 IPA 的降解效率则不受进料方式的影响。还研究了代表性的 WO3-N-TNS 样品上的正己烷转化为 CO2、光催化剂的耐用性和潜在的副产物形成。基于羟基自由基种群的测量,认为对于 WO3-N-TNS 光催化剂上的正己烷光催化分解,异质结型机制比直接 Z 型机制更合理。