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镍铜改性二氧化钛纳米管增强光催化降解扑热息痛:机理洞察与性能评估

Enhanced Photocatalytic Paracetamol Degradation by NiCu-Modified TiO Nanotubes: Mechanistic Insights and Performance Evaluation.

作者信息

Pinna Marco, Zava Martina, Grande Tommaso, Prina Veronica, Monticelli Damiano, Roncoroni Gianluca, Rampazzi Laura, Hildebrand Helga, Altomare Marco, Schmuki Patrik, Spanu Davide, Recchia Sandro

机构信息

Department of Science and High Technology, University of Insubria, Via Valleggio 11, 22100 Como, Italy.

Dipartimento di Chimica, Università Degli Studi di Milano, Via Golgi 19, 20133 Milan, Italy.

出版信息

Nanomaterials (Basel). 2024 Sep 29;14(19):1577. doi: 10.3390/nano14191577.

Abstract

Anodic TiO nanotube arrays decorated with Ni, Cu, and NiCu alloy thin films were investigated for the first time for the photocatalytic degradation of paracetamol in water solution under UV irradiation. Metallic co-catalysts were deposited on TiO nanotubes using magnetron sputtering. The influence of the metal layer composition and thickness on the photocatalytic activity was systematically studied. Photocatalytic experiments showed that only Cu-rich co-catalysts provide enhanced paracetamol degradation rates, whereas Ni-modified photocatalysts exhibit no improvement compared with unmodified TiO. The best-performing material was obtained by sputtering a 20 nm thick film of 1:1 atomic ratio NiCu alloy: this material exhibits a reaction rate more than doubled compared with pristine TiO, enabling the complete degradation of 10 mg L of paracetamol in 8 h. The superior performance of NiCu-modified systems over pure Cu-based ones is ascribed to a Ni and Cu synergistic effect. Kinetic tests using selective holes and radical scavengers unveiled, unlike prior findings in the literature, that paracetamol undergoes direct oxidation at the photocatalyst surface via valence band holes. Finally, Chemical Oxygen Demand (COD) tests and High-Resolution Mass Spectrometry (HR-MS) analysis were conducted to assess the degree of mineralization and identify intermediates. In contrast with the existing literature, we demonstrated that the mechanistic pathway involves direct oxidation by valence band holes.

摘要

首次研究了用镍、铜和镍铜合金薄膜修饰的阳极二氧化钛纳米管阵列在紫外光照射下对水溶液中扑热息痛的光催化降解性能。采用磁控溅射法在二氧化钛纳米管上沉积金属助催化剂。系统研究了金属层组成和厚度对光催化活性的影响。光催化实验表明,只有富铜助催化剂能提高扑热息痛的降解率,而镍改性的光催化剂与未改性的二氧化钛相比没有改善。性能最佳的材料是通过溅射一层20 nm厚、原子比为1:1的镍铜合金薄膜获得的:这种材料的反应速率比原始二氧化钛提高了一倍多,能够在8小时内完全降解10 mg/L的扑热息痛。镍铜改性体系比纯铜基体系具有更优异的性能,这归因于镍和铜的协同效应。使用选择性空穴和自由基清除剂的动力学测试揭示,与文献中先前的发现不同,扑热息痛在光催化剂表面通过价带空穴进行直接氧化。最后,进行了化学需氧量(COD)测试和高分辨率质谱(HR-MS)分析,以评估矿化程度并鉴定中间体。与现有文献不同,我们证明了其机理途径涉及价带空穴的直接氧化。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/323d/11477857/8667a6eac741/nanomaterials-14-01577-g001.jpg

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