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氢暴露下钯金合金薄膜与纳米颗粒的直接比较

Direct Comparison of PdAu Alloy Thin Films and Nanoparticles upon Hydrogen Exposure.

作者信息

Bannenberg Lars Johannes, Nugroho Ferry Anggoro Ardy, Schreuders Herman, Norder Ben, Trinh Thu Trang, Steinke Nina-Juliane, van Well Ad A, Langhammer Christoph, Dam Bernard

机构信息

Faculty of Applied Sciences , Delft University of Technology , Mekelweg 15 , 2629 JB Delft , The Netherlands.

Department of Physics , Chalmers University of Technology , 412 96 Göteborg , Sweden.

出版信息

ACS Appl Mater Interfaces. 2019 May 1;11(17):15489-15497. doi: 10.1021/acsami.8b22455. Epub 2019 Apr 18.

Abstract

Nanostructured metal hydrides are able to efficiently detect hydrogen in optical sensors. In the literature, two nanostructured systems based on metal hydrides have been proposed for this purpose each with its own detection principle: continuous sub-100 nm thin films read out via optical reflectance/transmittance changes and nanoparticle arrays for which the detection relies on localized surface plasmon resonance. Despite their apparent similarities, their optical and structural response to hydrogen has never been directly compared. In response, for the case of PdAu ( y = 0.15-0.30) alloys, we directly compare these two systems and establish that they are distinctively different. We show that the dissimilar optical response is not caused by the different optical readout principles but results from a fundamentally different structural response to hydrogen due to the different nanostructurings. The measurements empirically suggest that these differences cannot be fully accounted by surface effects but that the nature of the film-substrate interaction plays an important role and affects both the hydrogen solubility and the metal-to-metal hydride transition. In a broader perspective, our results establish that the specifics of nanoconfinement dictate the structural properties of metal hydrides, which in turn control the properties of nanostructured devices including the sensing characteristics of optical hydrogen sensors and hydride-based active plasmonic systems.

摘要

纳米结构金属氢化物能够在光学传感器中高效检测氢气。在文献中,已经提出了两种基于金属氢化物的纳米结构系统用于此目的,每种系统都有其自身的检测原理:通过光学反射率/透射率变化读出的连续亚100纳米薄膜,以及检测依赖于局域表面等离子体共振的纳米颗粒阵列。尽管它们表面相似,但它们对氢气的光学和结构响应从未被直接比较过。对此,对于PdAu(y = 0.15 - 0.30)合金的情况,我们直接比较了这两种系统,并确定它们有显著差异。我们表明,不同的光学响应不是由不同的光学读出原理引起的,而是由于不同的纳米结构导致对氢气的结构响应存在根本差异。测量结果凭经验表明,这些差异不能完全由表面效应来解释,而是薄膜 - 衬底相互作用的性质起着重要作用,并影响氢气溶解度和金属到金属氢化物的转变。从更广泛的角度来看,我们的结果表明纳米限域的具体情况决定了金属氢化物的结构性质,进而控制了纳米结构器件的性质,包括光学氢气传感器和基于氢化物的有源等离子体系统的传感特性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/22b7/6498406/e2182e41fe95/am-2018-224558_0001.jpg

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