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Plasmon-enhanced photocatalytic properties of nano Ag@AgBr on single-crystalline octahedral Cu2O (111) microcrystals composite photocatalyst

机译:纳米Ag @ AgBr在单晶八面体Cu2O(111)微晶复合光催化剂上的等离子体增强光催化性能

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A new composite photocatalyst Ag@AgBr/Cu2O was prepared by loading Ag@AgBr on (1 1 1) facts of octahedral Cu2O substrate via a facile precipitation in situ photoreduction method and characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), energy dispersive X-ray spectroscopy (EDX), ultraviolet-visible diffuse reflectance spectroscopy (UV-vis), nitrogen sorption and the photoelectrochemical measurements. The results show that Ag@AgBr nanoparticles are well-dispersed on Cu2O nanoparticles with narrow size distributions and controllable sizes from 10 to 30 nm. TEM results of the as-synthesized Ag@AgBr/Cu2O nanocomposite revealed that Ag@AgBr nanoparticles were attached to the surface of octahedral Cu2O. Photocatalytic degradation of methylene blue (MB) was carried out to evaluate the photocatalytic activity of Ag@AgBr/Cu2O under visible-light irradiation. The Ag@AgBr/Cu2O composite showed stronger visible light absorption capacity and higher photocatalytic activity than pure Cu2O. The Ag@AgBr (15 wt.%)/Cu2O sample presented the best photocatalytic activity, degrading 93.28% MB after irradiation for 90 min, due to their high surface area (18.499 m(2) g(-1)), the Crystal effect of Cu2O and surface plasmon resonance of Ag NPs. Meanwhile, phenol was degraded to further prove the degradation ability of Ag@AgBr/Cu2O. In addition, the quenching effect was examined in the photocatalytic reaction process of MB. Active h(+), Br-0 and the resulting center dot O-2(-) played the major roles for the dye degradation, while (OH)-O-center dot was verified to be insignificant. Based on the experimental results, a photocatalytic mechanism for organics degradation over Ag@AgBr/Cu2O photocatalysts was proposed. The electronic interactions were systematically studied and confirmed by the photoelectrochemical measurements. (C) 2015 Elsevier BY. All rights reserved.
机译:通过一种简便的原位光还原法将Ag @ AgBr负载在八面体Cu2O衬底的(1 1 1)面上,并通过X射线衍射(XRD),扫描电镜( SEM),透射电子显微镜(TEM),能量色散X射线光谱(EDX),紫外可见漫反射光谱(UV-vis),氮吸附和光电化学测量。结果表明,Ag @ AgBr纳米粒子良好地分散在Cu2O纳米粒子上,具有窄的尺寸分布和10至30 nm的可控制尺寸。合成后的Ag @ AgBr / Cu2O纳米复合材料的TEM结果表明,Ag @ AgBr纳米颗粒附着在八面体Cu2O的表面。对亚甲基蓝(MB)进行光催化降解,以评价Ag @ AgBr / Cu2O在可见光照射下的光催化活性。与纯Cu 2 O相比,Ag @ AgBr / Cu 2 O复合材料显示出更强的可见光吸收能力和更高的光催化活性。 Ag @ AgBr(15 wt。%)/ Cu2O样品表现出最佳的光催化活性,照射90分钟后降解93.28%MB,这是由于它们的高表面积(18.499 m(2)g(-1)),晶体Cu 2 O和Ag纳米颗粒表面等离子体共振的影响同时,苯酚被降解以进一步证明Ag @ AgBr / Cu2O的降解能力。另外,在MB的光催化反应过程中检查了猝灭作用。活性h(+),Br-0和生成的中心点O-2(-)在染料降解中起主要作用,而(OH)-O-中心点被证明是无关紧要的。基于实验结果,提出了Ag @ AgBr / Cu2O光催化剂降解有机物的光催化机理。对电子相互作用进行了系统的研究,并通过光电化学测量得到了证实。 (C)2015 Elsevier BY。版权所有。

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