光催化
光降解
罗丹明B
材料科学
催化作用
选区衍射
光化学
化学工程
降级(电信)
纳米技术
化学
有机化学
透射电子显微镜
电信
计算机科学
工程类
作者
Junwen Cai,Xin Jiang,Linfeng Zhang,Benoît Couturaud,W Tang,Yao-Yan Zhang,Rui‐Bo Jin,Yoann de Rancourt de Mimérand,Xiaoyun Jin,Jia Guo
标识
DOI:10.1021/acsanm.4c01664
摘要
A multifunctional, multiphase-supported photocatalyst was fabricated via the combination of LCD three-dimensional (3D) printing, cold plasma discharge (CPD) technology, and surface chemistry to be used for the degradation of organic pollutants in water and for the generation of hydrogen gas. BiOBr was chosen as the main catalytic phase and was used in association with a phosphor, SrAl2O4:Eu2+,Dy3+ (SAED), and a metal–organic framework, Ni-BDC. Their immobilization was realized thanks to polydopamine (PDA), which is used as a coupling agent. While BiOBr was the most active photocatalytic phase, the phosphor acted as a light-storing component for photodegradation in the dark and overall, as a boost for photoactivity. PDA also boosted the photoactivity, in parallel with its crucial role in the immobilization of the SAED/Ni-MOF/BiOBr catalyst on fractal polymer support. An in situ complexation-assisted precipitation (ISCAP) process was used, allowing the formation of the catalytic phases with nano features. The resulting hybrid photocatalysts were tested through rhodamine B (RhB) dye photodegradation upon visible light irradiation or light/dark alternating conditions to simulate more realistic variable light illumination. We found that, although used in a very small amount, the Ni-MOF had a significant impact on the photoactivity, forming a Z-scheme heterojunction with BiOBr. Finally, H2 evolution testing further established the photocatalytic activity and versatility of the supported catalysts.
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