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Surface plasmon-driven photoelectrochemical water splitting of TiO2 nanowires decorated with Ag nanoparticles under visible light illumination

机译:银纳米粒子修饰的TiO2纳米线的表面等离激元驱动光电化学水分解在可见光下

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摘要

Here, we demonstrate that TiO2 nanowires (NWs) can be significantly driven by visible light through the decoration with Ag nanoparticles (NPs) (Ag-decorated TiO2 NWs). The Ag-decorated TiO2 NWs show remarkably photoelectrochemical (PEC) water splitting performance under illumination with lambda > 420 visible light due to surface plasmon resonance (SPR) of Ag NPs. In this work, low power of the used light source (100 mW/cm(2)) was not capable of heating the Ag-decorated TiO2 nanowire photoanode enough to directly split water. In addition, under irradiation with lambda > 420 nm visible light, no photocurrent was produced by TiO2 nanowire photoanode indicates that electron transitions between valence band and conduction band do not take place in prepared anatase TiO2 NWs. Meanwhile, the SPR energy (2.95-2.13 eV < 3.2 eV) is insufficient to excite TiO2 NWs to generate electro-hole pairs through SPR-enhanced electromagnetic fields. Thus the remarkably visible-light-responsive PEC water splitting activity of Ag-decorated TiO2 NWs is not attributed to local heating caused by SPR-mediated photothermal process, large enhancement of electromagnetic fields induced by SPR and scattering of resonant photons. We propose that the visible light PEC water splitting performance of Ag-decorated TiO2 NWs is attributed to electron transfer from Ag NPs to the conduction band of TiO2 NWs mediated by SPR. In addition, a Schottky barrier established at the interface of Ag NPs and TiO2 NWs prevents these transferred electrons from returning to the Ag NPs and significantly retarded the recombination of electron-hole pairs in the Ag NPs, also contributing to visible-light-driven PEC water splitting performance. So the remarkably visible-light-driven PEC water splitting performance of Ag-decorated TiO2 NWs is attributed to the synergistic effects of electron transfer mediated by SPR and the Schottky barrier between Ag NPs and TiO2 NWs. The achieved Ag-decorated TiO2 NWs can be added to these previously prepared TiO2 photocatalysts mainly driven by SPR of Au NPs for the development of new visible light photocatalysts. (C) 2017 Elsevier B.V. All rights reserved.
机译:在这里,我们证明TiO2纳米线(NWs)可以由可见光显着驱动,该可见光穿过具有Ag纳米颗粒(NPs)(用Ag装饰的TiO2 NWs)的装饰。 Ag修饰的TiO2 NW由于Ag NP的表面等离振子共振(SPR),在λ> 420的可见光照射下表现出显着的光电化学(PEC)水分解性能。在这项工作中,所使用的光源的低功率(100 mW / cm(2))不能加热足够的Ag装饰的TiO2纳米线光电阳极以直接分解水。此外,在λ> 420 nm可见光照射下,TiO2纳米线光电阳极未产生光电流,这表明在制备的锐钛矿型TiO2 NW中价带和导带之间不发生电子跃迁。同时,SPR能量(2.95-2.13 eV <3.2 eV)不足以激发TiO2 NW通过SPR增强的电磁场产生电空穴对。因此,用Ag装饰的TiO2 NW的明显可见光响应的PEC水分解活性不归因于SPR介导的光热过程引起的局部加热,SPR诱导的电磁场的大幅度增强以及共振光子的散射。我们提出,用Ag修饰的TiO2 NWs的可见光PEC水分解性能是由于电子从Ag NPs转移到SPR介导的TiO2 NWs的导带。此外,在Ag NPs和TiO2 NWs界面处建立的肖特基势垒可防止这些转移的电子返回到Ag NPs中,并显着阻碍Ag NPs中电子-空穴对的重组,这也有助于可见光驱动的PEC水分解性能。因此,由Ag修饰的TiO2 NWs具有明显的可见光驱动的PEC水分解性能,这归因于SPR介导的电子转移和Ag NPs与TiO2 NWs之间的肖特基势垒的协同作用。可以将获得的经过Ag装饰的TiO2 NW添加到这些先前制备的主要由Au NP的SPR驱动的TiO2光催化剂中,以开发新的可见光光催化剂。 (C)2017 Elsevier B.V.保留所有权利。

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