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A Facile One-Pot Synthesis of Biomimetic Photocatalyst Zn(II)-Porphyrin-Sensitized 3D TiO2 Hollow Nanoboxes and Synergistically Enhanced Visible-Light Degradation

机译:仿生光催化剂Zn(II)-卟啉敏化的3D TiO2空心纳米盒的一锅法合成和协同增强的可见光降解

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摘要

A serials of biomimetic photocatalyst zinc(II) meso-tetra(4-carboxyphenyl)porphyrinato (ZnTCP)-sensitized 3D hierarchical TiO2 hollow nanoboxes (TiO2-HNBs) assembled by six ordered nanosheets with dominant {001} facets exposure (ZnTCP@TiO2-HNBs) have been successfully synthesized by a facile one-pot solvothermal method via a topological transformation process with TiOF2 as template. Infrared spectra (IR), UV-vis spectroscopy, and X-ray photoelectron spectroscopy (XPS) confirmed that ZnTCP played a decisive role in constructing 3D hollow nanoboxes through the formation of ester bond combined to TiO2-HNBs, which also provided a transferring photo excited electrons bridge to sensitize TiO2-HNBs for enhancing visible-light response. Due to the superior sensitization and biomimetic activity of ZnTCP, the photodegradation rate of rhodamine B (RhB) of as-prepared ZnTCP@TiO2-HNBs with ZnTCP/TiOF2 mass ratio of 2% (T-2p) improves 3.6 times compared to that of TiO2-HNBs with a degradation yield of 99% for 2 h under simulated sunlight irradiation (> 420 nm). The enhanced photodegradation ability was attributed to synergistic visible photocatalytic mechanism of biomimetic catalyst, which can not only produce hydroxyl radical (•OH) and superoxide radical (•O2) coming from the excitation process of ZnTCP sensitized TiO2-HNBs, but also generate singlet oxygen (1O2) that was only provided by biomimetic enzyme porphyrins. Furthermore, the photocatalyst showed good recycling stability and dispersibility after five rounds, ascribed to ZnTCP strong chemical bonding to the support TiO2-HNBs. By means of electrochemical cyclic voltammetry analysis, the effect of central zinc ions and parent porphyrin rings on the redox property of biomimetic catalyst was studied.
机译:一系列仿生光催化剂锌(II)介孔四(4-羧基苯基)卟啉锌(ZnTCP)敏化的3D分层TiO2空心纳米盒(TiO2-HNBs),由六个有序{001}面暴露的有序纳米片组装而成(ZnTCP @ TiO2- (HNBs)已经通过一种简便的一锅溶剂热法通过以TiOF2为模板的拓扑转化过程成功合成。红外光谱(IR),紫外可见光谱和X射线光电子能谱(XPS)证实ZnTCP通过与TiO2-HNB结合形成酯键,在构建3D空心纳米盒中起着决定性作用,后者还提供了转移光激发的电子桥使TiO2-HNB敏化以增强可见光响应。由于ZnTCP的优异的敏化性和仿生活性,所制备的ZnTCP / TiOF2质量比为2%(T-2p)的ZnTCP @ TiO2-HNBs的若丹明B(RhB)的光降解速率比ZnTCP @ TiO2-HNB提高3.6倍。 TiO2-HNBs在模拟太阳光照射下(> 420nm)降解2小时的产率为99%。增强的光降解能力归因于仿生催化剂的协同可见光催化机理,该机理不仅可以通过ZnTCP敏化的TiO2的激发过程产生羟自由基(•OH)和超氧化物自由基(•O2 -) -HNBs,但还会产生单线态氧( 1 O2),仅由仿生酶卟啉提供。此外,光催化剂在五轮后显示出良好的循环稳定性和分散性,这归因于ZnTCP与载体TiO2-HNB的牢固化学键合。通过电化学循环伏安法,研究了中心锌离子和母卟啉环对仿生催化剂氧化还原性能的影响。

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