Low-temperature synthesis of δ-Bi2O3 hierarchical nanostructures composed of ultrathin nanosheets for efficient photocatalysis

被引:52
作者
Sudrajat, Hanggara [1 ]
Sujaridworakun, Pornapa [1 ,2 ]
机构
[1] Chulalongkorn Univ, Fac Sci, Dept Mat Sci, Res Unit Adv Ceram, Bangkok 10330, Thailand
[2] Chulalongkorn Univ, Ctr Excellence Petrochem & Mat Technol, Bangkok 10330, Thailand
关键词
Bismuth oxide; Photocatalyst; UV light; Environmental remediation; Advanced oxidation process; OXIDE-ION CONDUCTIVITY; CONTROLLABLE SYNTHESIS; ROOM-TEMPERATURE; BISMUTH OXIDE; DEGRADATION; MECHANISM; VANADIUM; STABILIZATION; GROWTH; PHASE;
D O I
10.1016/j.matdes.2017.05.087
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
Due to its highest conductivity of any oxide material, the delta phase of Bi2O3 (delta-Bi2O3) is recognized as one of the most technologically important materials for various applications, including photocatalysis. Nevertheless, the delta-Bi2O3 phase is not stable at room temperature. Herein, we demonstrate that delta-Bi2O3 can be synthesized at low temperature through a facile sol-gel route in the presence of metavanadate oxyanion (VO3-). The chemical state and local structure of V are investigated by synchrotron-based techniques, such as X-ray absorption near edge structure (XANES) and extended X-ray absorption fine structure (EXAFS). Our findings demonstrate the critical role of VO3- in stabilizing the delta-Bi2O3 phase. The crystallinity of delta-Bi2O3 is dramatically increased by the addition of VO3-. In the absence of VO3-, amorphous product is obtained. The as-synthesized delta-Bi2O3 possesses 3D hierarchical nanostructures constructed by ultrathin nanosheets with a few nanometers thick (similar to 5 nm). The nanosheets are composed of ultrasmall nanoparticles in the range of 1-2 nm in size. Such a unique hierarchitecture of delta-Bi2O3 allows efficient light utilization due to multiple reflections and scattering, indicated by its excellent photocatalytic activity for the degradation and mineralization of atrazine in aqueous solution. [GRAPHICS] .
引用
收藏
页码:501 / 511
页数:11
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