微波辅助共沉淀法制备光还原CO2用铜修饰多氧氧酸盐(Na7(h30o)Nb6O19·14H2O)纳米棒

J. R. Souza, J. A. Torres, L. S. Ribeiro, J. Filho, Fabiana L. Santos, Nicholas Malgioglio, L. F. Gorup, A. H. Pinto, A. E. Nogueira
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引用次数: 0

摘要

通过太阳能手段减少二氧化碳已被讨论为减排的替代方案,这是未来可持续、无碳生产的基本主题。然而,从催化剂开始,选择有效的系统仍然是一个关键问题,特别是由于现有选择的活性较差。由于多金属氧酸盐具有半导体性质,作为一种很有前途的光催化剂得到了广泛的研究。然而,由于铌的反应活性低,缺乏可溶前体,pH范围窄,合成多氧氧酸盐的条件很严格。与文献不同,在本研究中,我们报告了一种简单的多氧膦酸盐合成方法。该合成方法在CO2光还原过程中具有加工时间和温度低、活性和选择性好等显著特点。结果表明,CO2还原反应效率高,CO2转化为CO的选择性高(92.5%)。此外,C2化合物(如乙酸酯)在反应体系的液相中产生。我们的研究结果具有重要意义,表明了多氧膦酸盐在CO2光还原中的潜力,这为控制与合成的竞争反应开辟了一条道路,从而提高了选择性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The Facile Microwave-Assisted Coprecipitation Route to Obtain Polyoxoniobate (Na7(H3O)Nb6O19·14H2O) Nanorods Modified with Copper for CO2 Photoreduction
The CO2 reduction by solar means has been discussed as an alternative to emission abatement, a fundamental topic for sustainable, carbon-free production in the future. However, the choice of efficient systems, starting with the catalysts, is still a critical issue, especially due to the poor activity of available options. Polyoxometalates have been extensively studied as promising photocatalysts due to their semiconducting properties. Nevertheless, the synthetic conditions of polyoxoniobate are stringent due to the low reaction activity of Nb species, the lack of soluble precursors, and the narrow pH range. Unlike the literature, in the present study, we report a simple polyoxoniobate synthesis method. This synthesis method has some remarkable features, such as low processing time and temperature and good activity and selectivity in the CO2 photoreduction process. The results revealed an outstanding efficiency for the CO2 reduction reaction with a high selectivity of CO2 to CO conversion (92.5%). Furthermore, C2 compounds (e.g., acetate) were produced in the liquid phase of the reaction system. Our findings are significant for indicating the potential of polyoxoniobate for CO2 photoreduction, which opens a way to control competitive reactions with synthesis, leading to higher selectivity.
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