The self-assembled gold nanoparticle (NP) superlattice displays unusual but distinctive features such as high mechanical and free-standing performance, electrical conductivity, and plasmonic properties, which are widely employed in various applications especially in biological diagnostics and optoelectronic devices. For a two-dimensional (2D) superlattice monolayer film composed of a given metal nanostructure, it is rather challenging to tune either its plasmonic properties or its optical properties in a reversible way, and it has not been reported. It is therefore of significant value to construct a free-standing 2D superlattice monolayer film of gold nanoparticles with an intelligent response and desired functions. Herein, we developed an easy and efficient approach to construct a gold nanoparticle superlattice film with a dual-responsive plasmonic switch. In this system, gold nanoparticles were coated by polyaniline (PANI) and then interracially self-assembled into a monolayer film at the air-liquid interface. The PANI shell plays two important roles in the superlattice monolayer film. First, the PANI shell acts as a physical spacer to provide a steric hindrance to counteract the van der Waals (vdW) attraction between densely packed nanoparticles (NPs), resulting in the formation of a superlattice by adjusting the thickness of the PANI shell. Second, the PANI shells provide the superlattice film with multiple stimuli such as electrical potential and pH change, leading to reversible optical and plasmonic responsiveness. The superlattice monolayer film can show a vivid color change from olive green to pink, or from olive green to violet by the change of the corresponding stimuli. Also, the localized surface plasmonic resonance (LSPR) of the superlattice monolayer film can be reversibly modulated by both by changing the local pH and applying an electric potential. Notably, a significant plasmonic shift of 157 nm can be achieved in the superlattice monolayer film when the PANI shell with a thickness of 35 nm and gold nanorods as a core were used. The superlattice monolayer film with dual-responsive plasmonic switches is promising for a range of potential applications in optoelectronic devices, plasmonic and colorimetric sensors, and surface-enhanced Raman scattering (SERS).
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http://dx.doi.org/10.1021/acsami.0c01983 | DOI Listing |
Nanotechnology
January 2025
Nanjing University of Posts and Telecommunications, Nanjing University of Posts and Telecommunications, Kuala Lumpur, Selangor, 50603, MALAYSIA.
Two-dimensional Transition Metal Dichalcogenides (2D TMDs) have garnered significant attention in the field of materials science due to their remarkable electronic and optoelectronic properties, including high carrier mobility and tunable band gaps. Despite the extensive research on various TMDs, there remains a notable gap in understanding the synthesis techniques and their implications for the practical application of monolayer tungsten disulfide (WS2) in optoelectronic devices. This gap is critical, as the successful integration of WS2 into commercial technologies hinges on the development of reliable synthesis methods that ensure high quality and uniformity of the material.
View Article and Find Full Text PDFDalton Trans
January 2025
Tyndall National Institute, University College Cork, Lee Maltings, Dyke Parade, Cork, T12 R5CP, Ireland.
Layered materials, such as tungsten dichalcogenides (TMDs), are being studied for a wide range of applications, due to their unique and varied properties. Specifically, their use as either a support for low dimensional catalysts or as an ultrathin diffusion barrier in semiconductor devices interconnect structures are particularly relevant. In order to fully realise these possible applications for TMDs, understanding the interaction between metals and the monolayer they are deposited on is of utmost importance.
View Article and Find Full Text PDFACS Appl Mater Interfaces
January 2025
RIKEN Center for Emergent Matter Science (CEMS), 2-1 Hirosawa, Wako, Saitama 351-0198, Japan.
A fluoroalkyl-containing electron acceptor (Y-SSM) is designed and synthesized to control the orientation of the benchmark non-fullerene acceptor Y6 in thin films. Due to the low surface energy of the two fluoroalkyl chains at the terminal part of Y-SSM, it spontaneously segregates to the film surface during spin coating, forming a monolayer of edge-on oriented Y-SSM. The Y-SSM monolayer leads to crystallization of the underlying Y6 to induce a standing-up orientation in the bulk of the films, which is strikingly different from pure Y6 films that tend to be a face-on orientation.
View Article and Find Full Text PDFBiosensors (Basel)
January 2025
CAS Key Laboratory of Coastal Environmental Processes and Ecological Remediation, Yantai Institute of Coastal Zone Research, Chinese Academy of Sciences, Yantai 264003, China.
High-sensitivity and repeatable detection of hydrophobic molecules through the surface-enhanced Raman scattering (SERS) technique is a tough challenge because of their weak adsorption and non-uniform distribution on SERS substrates. In this research, we present a simple self-assembly protocol for monolayer SERS mediated by 6-deoxy-6-thio-β-cyclodextrin (β-CD-SH). This protocol allows for the rapid assembly of a compact silver nanoparticle (Ag NP) monolayer at the oil/water interface within 40 s, while entrapping analyte molecules within hotspots.
View Article and Find Full Text PDFJ Phys Chem Lett
January 2025
College of Chemistry, Key Laboratory of Theoretical and Computational Photochemistry, Beijing Normal University, Beijing 100875, China.
The deposition of alkali metals on oxide surfaces has garnered significant interest due to their critical role in enhancing various catalytic processes. However, the atomic-scale characterization of these structures remains elusive, owing to the complex and competing interactions among the oxygen, the alkali metals, and the metal atoms within the oxides. In this work, we grew alkali metals (Na, K, Cs) on the copper oxide films on the Cu(111) surface and found the formation of hexagonally ordered monolayer films.
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