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Cobalt monoxide/tungsten trioxide p-n heterojunction boosting charge separation for efficient visible-light-driven gaseous toluene degradation

机译:钴一氧化钴/钨三氧化钨P-N异质结升压电荷分离,用于高效可见光驱动的气态甲苯降解

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摘要

A novel cobalt monoxide/tungsten trioxide p -n heterojunction was fabricated via a two-step hydrothermal method for improving the photocatalytic activity for gaseous pollutant degradation and oxygen evolution. The TEM characterization results indicated that the CoO nanoparticles with diameter of 30 nm were uniformly distributed on the surface of WO3 nanoplates, which not only increased the light absorption efficiency but also promoted charge separation efficiency owing to a formed internal electric field in p -n junction hybridized system. In all samples, 15 wt% CoO/WO3 displayed the highest photocatalytic activity, where the degradation conversion of toluene achieved to 85.4% in 4 h, which were 2.0and 20.3-folds higher than that of WO3 and CoO, respectively. Besides, the as-prepared CoO/WO3 composite also exhibited significantly increased photo catalytic oxygen production under visible light irradiation. Moreover, by in-situ infrared spectra, the main intermediate products, including benzyl alcohol, benzaldehyde, benzoic acid and formate or acetate were clearly clarified at the interface over the catalysts. Combined with the ESR, VB-XPS and UPS, a possible mechanism for the photocatalytic process over the CoO/WO3 p-n heterojunctions were proposed and discussed.
机译:通过两步水热法制造了一种新型钴一氧化钴/钨三氧化物P-N异质结,用于改善气态污染物降解和氧气进化的光催化活性。 TEM表征结果表明,直径为30nm的官方纳米颗粒在WO3纳米间板的表面上均匀地分布,这不仅增加了光吸收效率,而且由于P-n结的形成内部电场而促进了电荷分离效率杂交的系统。在所有样品中,15wt%的CoO / WO3显示出最高的光催化活性,其中甲苯的降解转化为85.4%,分别比WO3和COO高2.0和20.3倍。此外,在可见光照射下,如制备的CoO / WO3复合材料也显着增加了光催化氧产量。此外,通过原位红外光谱,在催化剂上的界面处清楚地清楚地阐明包括苄醇,苯甲醛,苯甲酸和甲酸盐或乙酸酯的主要中间产物。结合ESR,VB-XPS和UPS,提出并讨论了在COO / WO3 P-N异质结上光催化过程的可能机制。

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