纳米片
光催化
材料科学
化学工程
电子顺磁共振
苯酚
催化作用
降级(电信)
涂层
激进的
光化学
光谱学
纳米技术
化学
有机化学
核磁共振
电信
物理
量子力学
计算机科学
工程类
作者
Yingying Wang,Wenjun Jiang,Wenjiao Luo,Xianjie Chen,Yongfa Zhu
标识
DOI:10.1016/j.apcatb.2018.06.013
摘要
In this work, ultrathin nanosheet g-C3N4@Bi2WO6 core-shell structure is fabricated by a new method of CN precursor in situ coating and low temperature reassembled. The CN small molecules were successfully polymerized to form ultrathin g-C3N4 layer (about 1 nm) on the surface of Bi2WO6 nanosheet under low temperature. And the g-C3N4@Bi2WO6 photocatalyst with 1 nm thickness of shell layers has the highest photocatalytic degradation phenol activity with visible light irradiation which is almost 5.7 times as high as that of bulk g-C3N4 and also 1.9 times compare to Bi2WO6 nanosheet. Simultaneously, phenol degradation activity by using g-C3N4@Bi2WO6 photocatalyst under full spectrum is 3.3 times that of bulk g-C3N4 and 1.5 times that of Bi2WO6 nanosheet. Superoxide radicals (O2−) and hydroxyl radicals (OH) as the main oxidative species proved by electron spin resonance spectroscopy (ESR). The interface catalytic system was found, that is the interface between the Bi2WO6 core and g-C3N4 shell effectively promote the phenol degradation activity revealed through a comprehensive contrast experiment. The establishment of g-C3N4@Bi2WO6 core-shell catalytic system can offer blueprints for the construction of other new interface catalytic system.
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