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基于三维等离子体结构实现的光致 Dember 效应驱动的整体水分解。

Light-Driven Overall Water Splitting Enabled by a Photo-Dember Effect Realized on 3D Plasmonic Structures.

机构信息

State Key Laboratory of Metal Matrix Composites, ‡School of Environmental Science and Engineering, and §Zhiyuan College, Shanghai Jiao Tong University , Shanghai 200240, China.

出版信息

ACS Nano. 2016 Jul 26;10(7):6693-701. doi: 10.1021/acsnano.6b01999. Epub 2016 Jun 30.

Abstract

Photoelectric conversion driven by sunlight has a broad range of energy/environmental applications (e.g., in solar cells and water splitting). However, difficulties are encountered in the separation of photoexcited charges. Here, we realize a long-range (∼1.5 μm period) electric polarization via asymmetric localization of surface plasmons on a three-dimensional silver structure (3D-Ag). This visible-light-responsive effect-the photo-Dember effect, can be analogous to the thermoelectric effect, in which hot carriers are thermally generated instead of being photogenerated. The induced electric field can efficiently separate photogenerated charges, enabling sunlight-driven overall water splitting on a series of dopant-free commercial semiconductor particles (i.e., ZnO, CeO2, TiO2, and WO3) once they are combined with the 3D-Ag substrate. These photocatalytic processes can last over 30 h on 3D-Ag+ZnO, 3D-Ag+CeO2, and 3D-Ag+TiO2, thus demonstrating good catalytic stability for these systems. Using commercial WO3 powder as a reference, the amount of O2 generated with 3D-Ag+CeO2 surpasses even its recently reported counterpart in which sacrificial reagents had to be involved to run half-reactions. This plasmon-mediated charge separation strategy provides an effective way to improve the efficiency of photoelectric energy conversion, which can be useful in photovoltaics and photocatalysis.

摘要

基于阳光的光电转换在能源/环境应用领域(例如太阳能电池和水分解)有广泛的应用。然而,在光激发电荷的分离方面仍存在困难。在这里,我们通过在三维银结构(3D-Ag)上的表面等离激元的不对称局域化实现了长程(∼1.5μm 周期)的电极化。这种可见光响应的效应——光德姆效应,可以类比于热电效应,其中热载流子是通过热生成而不是光生成的。所诱导的电场可以有效地分离光生电荷,从而使一系列无掺杂商用半导体颗粒(即 ZnO、CeO2、TiO2 和 WO3)在与 3D-Ag 基底结合后能够进行阳光驱动的整体水分解。这些光催化过程在 3D-Ag+ZnO、3D-Ag+CeO2 和 3D-Ag+TiO2 上可以持续超过 30 小时,从而证明了这些体系具有良好的催化稳定性。使用商用 WO3 粉末作为参考,3D-Ag+CeO2 产生的 O2 量甚至超过了其最近报道的需要使用牺牲试剂来运行半反应的对应物。这种等离子体介导的电荷分离策略为提高光电能量转换效率提供了一种有效途径,可用于光伏和光催化。

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