Fabrication of PVDF/TiO2@CQDs photocatalytic films by ink-jet printing for dye degradation under visible light

制作 降级(电信) 光催化 材料科学 墨水池 可见光谱 化学工程 复合材料 光电子学 纳米技术 化学 催化作用 有机化学 医学 电信 替代医学 病理 计算机科学 工程类
作者
Zihan Tian,Shuhao Qin,Jingkui Yang,Xiao Wu,Jing Zhang,Jianxin Li,Hong Wang,Zhenyu Cui
出处
期刊:Applied Surface Science [Elsevier BV]
卷期号:661: 160078-160078 被引量:1
标识
DOI:10.1016/j.apsusc.2024.160078
摘要

PVDF/TiO2@CQDs hybrid photocatalytic thin films were prepared by ink-jet printing. The printing ink was prepared with the TiO2, TiO2(s)@CQDs (surface composite), and TiO2(i)@CQDs (situ doping) nanoparticles as precursors, respectively. Compared to TiO2(s)@CQDs, TiO2(i)@CQDs has a smaller particle size (about 10.01 nm) and a narrower particle size distribution (6∼14 nm), which can improve the photocatalytic effect while avoiding nozzle clogging. The PVDF/TiO2(i)@CQDs hybrid film exhibited a high degradation efficiency (η) of 93.71 % for Rhodamine B (RhB) within 150 min under visible light with a catalyst load of only 0.49 wt%. The reaction rate constant (ks) of the PVDF/TiO2(i)@CQDs film was about 4.3 times higher than that of the PVDF/TiO2(s)@CQDs film. The small particle size of this S-scheme TiO2(i)@CQDs heterostructure nanoparticle and the more effective contact interface formed between TiO2 and carbon quantum dots (CQDs) further facilitated electron transfer and enhanced photoactivity. The firmly immobilized catalysts on the Polyvinylidene fluoride (PVDF) film substrate through Ti-F coordination bonds ensured the reusability and stability of the photocatalytic film (the η of RhB still reached 88.05 % after 10 consecutive cycles). This work provides a new strategy for the application of ink-jet printing technology in photocatalysis.
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