Regulating the Electronic Structure of Fe3+-Doped BiOClxl1-x Solid Solution by an Amidoxime-Functionalized Fibrous Support for Efficient Photocatalysis

被引:22
|
作者
Han, Zhenbang [1 ,2 ]
Lv, Mingze [1 ]
Shi, Xianbing [1 ]
Li, Guobin [1 ]
Zhao, Jin [1 ,2 ]
Zhao, Xiaoming [1 ,2 ]
机构
[1] Tiangong Univ, Sch Text Sci & Engn, Tianjin 300387, Peoples R China
[2] Tianjin Municipal Key Lab Adv Fiber & Energy Stor, Tianjin 300387, Peoples R China
基金
中国国家自然科学基金;
关键词
Bismuth oxyhalides; Fe doping; Fiber-based catalyst; Photocatalytic degradation; OXYGEN VACANCY; EFFECTIVE CATALYST; PAN FIBER; BIOCL; ACTIVATION; WATER; DEGRADATION; FE/BIOCL; DESIGN; TIO2;
D O I
10.1007/s42765-022-00220-0
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
BiOX (X= Cl, I, Br) has attracted intensive interest as a photocatalyst for environmental remediation, but its limited photocatalytic activity versus visible light irradiation restricts its practical application. Herein, a Fe3+-doped BiOCl(x)l(1-x) solid solution (Fe-BiOCl(x)l(1-x)) was synthesized in situ on an amidoxime-functionalized fibrous support via a one-pot solvothermal approach. Comprehensive characterization and DFT calculations indicate that the robust chelated interaction between amidoxime groups and Fe3+ greatly boosts the crystal growth of nanosized Fe-BiOCl(x)l(1-x) on the fibrous surface, simultaneously tunes its electronic structure for improved light harvesting and oxygen vacancy creation, and enables the fibrous support to act as an electron sink for efficient charge separation. These synergistic qualities result in high photocatalytic activity for the degradation of organic contaminants, which outperforms that obtained for unsupported Fe-BiOCl(x)l(1-x) and other fibrous samples by several times. Our findings highlight the importance of functionalized support design for the development of efficient BiOX photocatalysts under visible light irradiation.
引用
收藏
页码:266 / 281
页数:16
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