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首页> 外文期刊>Computational Materials Science >Enhancing photocatalytic activity for hydrogen production and pollutant degradation by modifying tetragonal ZrO2 with monolayers slab surface of BiVO4, Ag3PO4, SrTiO3 and WO3: A first-principles study
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Enhancing photocatalytic activity for hydrogen production and pollutant degradation by modifying tetragonal ZrO2 with monolayers slab surface of BiVO4, Ag3PO4, SrTiO3 and WO3: A first-principles study

机译:通过改性Bivo4,Ag3PO4,Srtio3和WO3的单层ZrO2改变四边形ZrO2,增强氢催化活性和污染物降解的光催化活性:第一原理研究

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Semiconductor-based photocatalysis has received increasing attention in energy storage and environmental remediation process due to the abundant solar energy. For this purpose, heterostructures of ZrO2 coupled with BiVO4, Ag3PO4, SrTiO3 and WO3 monolayers are designed to examine their potential applications in hydrogen production and degradation of pollutants using density functional theory (DFT) + U method for the first time. The results revealed that the calculated band gaps of the heterostructures are reduced compared to the pure ZrO2, which favour redshift absorption. A type-I band alignment is attained for the BiVO4/ZrO2, Ag3PO4/ZrO2 and WO3/ZrO2 heterostructures. More importantly, a type-II staggered band alignment formed in the SrTiO3/ZrO2 heterostructure restrained the charge recombination rate of photoinduced charge carriers, as well as enhancing the photocatalytic activity. In particular, suitable band alignment of SrTiO3/ZrO2 with enough driving forces for charge carrier transfer show overall water splitting and degradation of pollutant in which SrTiO3 acted as charge separation centre. Furthermore, h(+), and radicals played a major role in the photocatalysis process of the SrTiO3/ZrO2 heterostructure. These results reveal that the ZrO2 acts as an oxidation site so that better access of electron acceptor to the interface is a significant factor that improves the photocatalytic activity of SrTiO3/ZrO2 heterostructure towards H-2 evolution. (C) 2017 Elsevier B.V. All rights reserved.
机译:由于太阳能丰富,基于半导体的光催化在能量储存和环境修复过程中受到了越来越关注。为此目的,ZrO2与BiVO4,Ag3PO4,Srtio3和WO3单层偶联的异质结构设计用于首次使用密度官能理论(DFT)+ U方法在氢气产生和降解污染物中的潜在应用。结果表明,与纯ZrO2相比,异质结构的计算带间隙减少,这有利于红移吸收。对BIVO4 / ZrO2,Ag3PO4 / ZrO2和WO3 / ZrO2异质结构达到了I型频带对准。更重要的是,在SRTIO3 / ZrO2异质结构中形成的II型交错带对准抑制了光致电荷载体的电荷重组率,以及增强光催化活性。特别地,SRTIO3 / ZrO2的合适带对准具有足够的驱动力用于电荷载体转移,显示出污染物的总水分裂和降解,其中Srtio3充当电荷分离中心。此外,H(+)和自由基在SRTIO3 / ZrO2异质结构的光催化过程中起主要作用。这些结果表明,ZrO2用作氧化位点,使电子受体更好地进入界面是改善SrtiO3 / ZrO2异质结构朝向H-2进化的光催化活性的重要因素。 (c)2017 Elsevier B.v.保留所有权利。

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