Evidence map›Paper›PMID 35542872›Full record

ArticleRSC advances2019

Manipulating the confinement of electromagnetic field in size-specific gold nanoparticles dimers and trimers.

Sudip Kumar Pal, Hirak Chatterjee, Sujit Kumar Ghosh

Abstract read
In one paragraph

Article in RSC advances, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

  1. Article
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

3 authors.

Sudip Kumar PalDepartment of Chemistry, Assam University Silchar-788011 Assam India sujit.kumar.ghosh@aus.ac.in +91-3842-270848.
Hirak ChatterjeeDepartment of Chemistry, Assam University Silchar-788011 Assam India sujit.kumar.ghosh@aus.ac.in +91-3842-270848.
Sujit Kumar GhoshDepartment of Chemistry, Assam University Silchar-788011 Assam India sujit.kumar.ghosh@aus.ac.in +91-3842-270848.ORCID https://orcid.org/0000-0001-6657-7396

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The intriguing light-matter interactions can be governed by controlling the particle size and shape, electromagnetic interactions and dielectric properties and local environment of the metal nanostructures. Amongst the different approaches that have been engendered to manipulate light at the nanoscale, the self-assembly of metallic nanostructures with controllable interparticle distances and angular orientations, which strongly impact their optical attributes, is one of the viable avenues to exploit their utility in a diverse range of niche applications. The simplest geometrical architectures that enable such modulations are dimers with changeable interparticle distances and trimers with an additional degree of angular orientation to correlate the plasmonic observables with the observed spectral characteristics. Wet chemical approaches have been adopted in this study for the synthesis of size-selective gold nanoparticles, and appropriate organic linkers have judiciously been employed to induce plasmonic interactions amongst the gold nanoparticles in close proximity to each other. The combination of experimental observations and electromagnetic simulations adopted to probe the plasmonic interactions revealed that the electrodynamic coupling effect was very sensitive to particle size, interparticle distances and angular orientations in these simple nanoassemblies. The capability to precisely manipulate the electric field at the junctions between these plasmon-coupled nanoparticles could pave the way for the application of these nanoassemblies in surface-enhanced spectroscopies and sensing applications.

Identifiers

PMID35542872
PMCPMC9076545

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.