Research Institute of Photocatalysis, Fujian Provincial Key Laboratory of Photocatalysis-State Key Laboratory Breeding Base, Fuzhou University, Fuzhou 350002, P R China.
Phys Chem Chem Phys. 2013 Aug 14;15(30):12742-7. doi: 10.1039/c3cp51247a.
TaON nanoparticles with low surface reduction defect sites were successfully constructed by a simple nitridation approach using Ta2O5·nH2O as a precursor. Large amounts of crystal water in Ta2O5·nH2O are considered as a parclose to prohibit Ta(5+) from being reduced in the nitridation process with NH3 gas. Urea was also used in the synthesis, acting as a co-nitridation agent together with NH3 but also as a porogen for creating nanopores in TaON frameworks. The as-prepared TaON catalyst was evaluated by environmental purification of organic pollutants in water, as exemplified here by mineralization of phenol and its chloroderivatives in aqueous phase under visible light irradiation. Results revealed that a lower defect density of TaON, as well as its nanopore structure and smaller particle size, contribute to the promotion in both electron-hole separation and interfacial charge-transfer in materials surface/interface, being the main reasons for the enhanced photocatalytic performance.
采用 Ta2O5·nH2O 作为前驱体,通过简单的氮化法成功构建了具有低表面还原缺陷位的 TaON 纳米粒子。大量的 Ta2O5·nH2O 晶水被认为是一种封闭物,阻止 Ta(5+)在与 NH3 气体的氮化过程中被还原。在合成中还使用了尿素,它不仅与 NH3 一起作为共氮化剂,而且还作为 TaON 框架中纳米孔的造孔剂。通过在水中净化有机污染物来评估所制备的 TaON 催化剂,这里举例说明了在可见光照射下,水中苯酚及其氯代衍生物的矿化作用。结果表明,TaON 的缺陷密度较低,以及其纳米孔结构和较小的颗粒尺寸,有助于促进材料表面/界面中的电子-空穴分离和界面电荷转移,这是增强光催化性能的主要原因。