Soft-hard templating solution combustion synthesized CeO2-CuO-TiO2 nanostructures for visible light photocatalysis

IF 5.3 2区 化学 Q1 CHEMISTRY, APPLIED Catalysis Today Pub Date : 2025-03-15 Epub Date: 2024-12-18 DOI:10.1016/j.cattod.2024.115169
Francesca Deganello , Massimo Dell’Edera , Leonarda Francesca Liotta , Roberto Comparelli , Maria Lucia Curri
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Abstract

Given the growing need to address emerging contaminants in water systems, particularly pharmaceutical compounds, there is a pressing demand for advanced and eco-friendly technologies capable of effectively degrading these pollutants. Heterogeneous photocatalysts, especially those based on TiO2, have shown considerable promise in water purification efforts. However, TiO2’s efficiency is primarily confined to the ultraviolet region (< 380 nm) due to its large band gap energy (3.2 eV) in the anatase phase. To overcome this limitation and extend the use of TiO2-based photocatalysts to the visible light spectrum, combining titania with other oxides that are sensitive to visible light has proven to be a successful strategy. Ceria (CeO2), with its Ce3 +/Ce4+ redox pair, enhances photocatalytic activity, while CuO is recognized for its ability to promote visible light responsiveness in TiO2 catalysts. This study explores a one-pot soft-hard templating Solution Combustion Synthesis (SCS) approach to prepare a series of CeO2-CuO-TiO2 nanostructures with different compositions, as effective heterogeneous photocatalysts for visible light-assisted degradation of organic contaminants. The performance of these photocatalysts was investigated both under UV and visible light irradiation, for methylene blue and nalidixic acid degradation, respectively, and compared to those of commercially available TiO2 nanomaterials used as references. Structural, morphological, textural, and redox analyses demonstrate that the synergistic interaction between the CeO2 and CuO phases with TiO2 significantly boosts the photocatalytic performance, particularly under visible light. Notably, the-top performing ternary photocatalyst reached a degradation rate of 62.9 % in 90 min, surpassing the reference TiO2 P25, which achieved 45 % under the same experimental conditions. The study highlights the potential of SCS as an effective synthetic method for producing nanostructured materials with controlled composition and structure. This approach promisingly addresses the environmental challenge of degrading organic contaminants in water using visible light.
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软硬模板溶液燃烧合成CeO2-CuO-TiO2纳米结构用于可见光光催化
鉴于日益需要解决水系统中新出现的污染物,特别是药物化合物,迫切需要能够有效降解这些污染物的先进和环保技术。非均相光催化剂,特别是基于TiO2的光催化剂,在水净化方面显示出相当大的前景。然而,TiO2的效率主要局限于紫外区(<;380 nm),这是由于锐钛矿相的带隙能量大(3.2 eV)。为了克服这一限制并将二氧化钛基光催化剂的使用扩展到可见光光谱,将二氧化钛与其他对可见光敏感的氧化物结合已被证明是一种成功的策略。铈(CeO2)的Ce3 +/Ce4+氧化还原对增强了光催化活性,而CuO在TiO2催化剂中具有促进可见光响应的能力。本研究探索了一锅软-硬模板溶液燃烧合成(SCS)方法,制备了一系列不同组成的CeO2-CuO-TiO2纳米结构,作为可见光辅助降解有机污染物的有效非均相光催化剂。研究了这些光催化剂在紫外和可见光照射下降解亚甲基蓝和萘啶酸的性能,并与市售TiO2纳米材料进行了比较。结构、形态、织构和氧化还原分析表明,CeO2和CuO相与TiO2之间的协同作用显著提高了光催化性能,特别是在可见光下。值得注意的是,性能最好的三元光催化剂在90 min内的降解率达到62.9 %,超过了参考TiO2 P25在相同实验条件下的45 %。该研究突出了SCS作为一种有效的合成方法的潜力,用于生产具有可控成分和结构的纳米结构材料。这种方法有望解决利用可见光降解水中有机污染物的环境挑战。
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来源期刊
Catalysis Today
Catalysis Today 化学-工程:化工
CiteScore
11.50
自引率
3.80%
发文量
573
审稿时长
2.9 months
期刊介绍: Catalysis Today focuses on the rapid publication of original invited papers devoted to currently important topics in catalysis and related subjects. The journal only publishes special issues (Proposing a Catalysis Today Special Issue), each of which is supervised by Guest Editors who recruit individual papers and oversee the peer review process. Catalysis Today offers researchers in the field of catalysis in-depth overviews of topical issues. Both fundamental and applied aspects of catalysis are covered. Subjects such as catalysis of immobilized organometallic and biocatalytic systems are welcome. Subjects related to catalysis such as experimental techniques, adsorption, process technology, synthesis, in situ characterization, computational, theoretical modeling, imaging and others are included if there is a clear relationship to catalysis.
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