scholarly journals Ultrathin Oxide Wrapping of Plasmonic Nanoparticles via Colloidal Electrostatic Self-Assembly and their Enhanced Performances

Author(s):  
Haoming Bao ◽  
Hongwen Zhang ◽  
Guangqiang Liu ◽  
Weiping Cai
Nano Letters ◽  
2012 ◽  
Vol 12 (2) ◽  
pp. 955-963 ◽  
Author(s):  
Bohdan Senyuk ◽  
Julian S. Evans ◽  
Paul J. Ackerman ◽  
Taewoo Lee ◽  
Pramit Manna ◽  
...  

2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Matthew T. Gole ◽  
Zhewen Yin ◽  
Michael Cai Wang ◽  
Wayne Lin ◽  
Ziran Zhou ◽  
...  

AbstractHierarchical heterostructures of two-dimensional (2D) nanomaterials are versatile platforms for nanoscale optoelectronics. Further coupling of these 2D materials with plasmonic nanostructures, especially in non-close-packed morphologies, imparts new metastructural properties such as increased photosensitivity as well as spectral selectivity and range. However, the integration of plasmonic nanoparticles with 2D materials has largely been limited to lithographic patterning and/or undefined deposition of metallic structures. Here we show that colloidally synthesized zero-dimensional (0D) gold nanoparticles of various sizes can be deterministically self-assembled in highly-ordered, anisotropic, non-close-packed, multi-scale morphologies with templates designed from instability-driven, deformed 2D nanomaterials. The anisotropic plasmonic coupling of the particle arrays exhibits emergent polarization-dependent absorbance in the visible to near-IR regions. Additionally, controllable metasurface arrays of nanoparticles by functionalization with varying polymer brushes modulate the plasmonic coupling between polarization dependent and independent assemblies. This self-assembly method shows potential for bottom-up nanomanufacturing of diverse optoelectronic components and can potentially be adapted to a wide array of nanoscale 0D, 1D, and 2D materials.


Nanoscale ◽  
2015 ◽  
Vol 7 (3) ◽  
pp. 956-964 ◽  
Author(s):  
Weikun Li ◽  
Istvan Kanyo ◽  
Chung-Hao Kuo ◽  
Srinivas Thanneeru ◽  
Jie He

The two-step pH-programmable self-assembly generates sophisticated “multi-block” chains.


2021 ◽  
Vol 9 ◽  
Author(s):  
Yun Liu ◽  
Weihua Fu ◽  
Zhongsheng Xu ◽  
Liang Zhang ◽  
Tao Sun ◽  
...  

Owing to the localized surface plasmon resonance (LSPR), dynamic manipulation of optical properties through the structure evolution of plasmonic nanoparticles has been intensively studied for practical applications. This paper describes a novel method for direct reversible self-assembly and dis-assembly of Au nanoparticles (AuNPs) in water driven by pH stimuli. Using 3-aminopropyltriethoxysilane (APTES) as the capping ligand and pH-responsive agent, the APTES hydrolyzes rapidly in response to acid and then condenses into silicon. On the contrary, the condensed silicon can be broken down into silicate by base, which subsequently deprotonates the APTES on AuNPs. By controlling condensation and decomposition of APTES, the plasmonic coupling among adjacent AuNPs could be reversible tuned to display the plasmonic color switching. This study provides a facile and distinctive strategy to regulate the reversible self-assembly of AuNPs, and it also offers a new avenue for other plasmonic nanoparticles to adjust plasmonic properties via reversible self-assembly.


Polymers ◽  
2020 ◽  
Vol 12 (10) ◽  
pp. 2381
Author(s):  
Gina M. DiSalvo ◽  
Abby R. Robinson ◽  
Mohamed S. Aly ◽  
Eric R. Hoglund ◽  
Sean M. O’Malley ◽  
...  

The self-assembly of amphiphilic diblock copolymers into polymeric vesicles, commonly known as polymersomes, results in a versatile system for a variety of applications including drug delivery and microreactors. In this study, we show that the incorporation of hydrophobic plasmonic nanoparticles within the polymersome membrane facilitates light-stimulated release of vesicle encapsulants. This work seeks to achieve tunable, triggered release with non-invasive, spatiotemporal control using single-pulse irradiation. Gold nanoparticles (AuNPs) are incorporated as photosensitizers into the hydrophobic membrane of micron-scale polymersomes and the cargo release profile is controlled by varying the pulse energy and nanoparticle concentration. We have demonstrated the ability to achieve immediate vesicle rupture as well as vesicle poration resulting in temporal cargo diffusion. Additionally, changing the pulse duration, from femtosecond to nanosecond, provides mechanistic insight into the photothermal and photomechanical contributors that govern membrane disruption in this polymer–nanoparticle hybrid system.


2021 ◽  
Author(s):  
David Vila-Liarte ◽  
Nicholas A. Kotov ◽  
Luis M. Liz-Marzán

Diverse templating materials and assembly strategies can be used to induce collective optical activity on achiral plasmonic building blocks. We present the advances, applications, challenges, and prospects of plasmonic–excitonic hybrids.


2017 ◽  
Vol 139 (6) ◽  
pp. 2345-2350 ◽  
Author(s):  
Joseph J. Armao ◽  
Irina Nyrkova ◽  
Gad Fuks ◽  
Artem Osypenko ◽  
Mounir Maaloum ◽  
...  

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