Evidence map›Paper›PMID 41304090›Full record

ArticleMaterials (Basel, Switzerland)2025

Stabilizing the Localized Surface Plasmon Resonance (LSPR) of Citrate-Synthesized Metal Nanoparticles in Organic Solvents.

Jacob P Magdon, Matthew J Jasienski, Madison R Waltz, Gabrielle A Grzymski, Calvin Chen, Arion M Solomon, Minh Dang Nguyen, Jong Moon Lee, John C Deàk, T Randall Lee and 1 more

Abstract read
In one paragraph

Article in Materials (Basel, Switzerland), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Article
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

11 authors.

Jacob P MagdonDepartment of Chemistry, University of Scranton, 800 Linden Street, Scranton, PA 18510, USA.ORCID 0009-0005-4197-878X
Matthew J JasienskiDepartment of Chemistry, University of Scranton, 800 Linden Street, Scranton, PA 18510, USA.ORCID 0009-0008-5167-2014
Madison R WaltzDepartment of Chemistry, University of Scranton, 800 Linden Street, Scranton, PA 18510, USA.ORCID 0009-0003-0367-5150
Gabrielle A GrzymskiDepartment of Chemistry, University of Scranton, 800 Linden Street, Scranton, PA 18510, USA.
Calvin ChenDepartment of Chemistry, University of Scranton, 800 Linden Street, Scranton, PA 18510, USA.
Arion M SolomonDepartment of Chemistry, University of Scranton, 800 Linden Street, Scranton, PA 18510, USA.ORCID 0009-0009-0983-7070
Minh Dang NguyenDepartment of Chemistry and the Texas Center for Superconductivity, University of Houston, 4800 Calhoun Road, Houston, TX 77204-5003, USA.ORCID 0000-0002-2569-8279
Jong Moon LeeDepartment of Chemistry and the Texas Center for Superconductivity, University of Houston, 4800 Calhoun Road, Houston, TX 77204-5003, USA.ORCID 0000-0002-2590-6031
John C DeàkDepartment of Chemistry, University of Scranton, 800 Linden Street, Scranton, PA 18510, USA.
T Randall LeeDepartment of Chemistry and the Texas Center for Superconductivity, University of Houston, 4800 Calhoun Road, Houston, TX 77204-5003, USA.ORCID 0000-0001-9584-8861
Riddhiman MedhiDepartment of Chemistry, University of Scranton, 800 Linden Street, Scranton, PA 18510, USA.ORCID 0000-0002-2368-2468

Funding

Air Force Office of Scientific Research 23RT0567Air Force Office of Scientific Research FA9550-23-1-0581Robert A. Welch Foundation E-1320Robert A. Welch Foundation V-E-0001
6 · The paper itself

Abstract

Gold-silver nanoshells (GS-NSs) are hollow spherical nanoparticles with an alloyed Ag-Au shell. GS-NSs exhibit a tunable localized surface plasmon resonance (LSPR) in the visible to near-IR wavelengths as a function of composition and shell thickness and offer greater stability across pH ranges compared to other metal nanoparticles. These properties make GS-NSs promising materials for diagnostics, photothermal therapy, and photocatalysis. However, current research has explored GS-NSs only in aqueous systems, since they immediately aggregate in other solvents, limiting their utility. This paper provides an in-depth study of the choice and effect of non-thiol ligands on the stability and phase-transfer of GS-NSs from aqueous to non-aqueous solvents, such as ethylene glycol, tetrahydrofuran, dichloromethane, and toluene. Ligand exchange for functionalization of GS-NSs was performed with Triton X-100 (TX100), sodium stearate (NaSt), polyvinylpyrrolidone (PVP), and hydroxypropyl cellulose (HPC), prior to phase-transfer. The nanoparticles were phase-transferred to the non-aqueous solvents, and the stability of the colloids in the various solvents before and after functionalization was recorded with UV-visible spectroscopy, dynamic light scattering (DLS), zeta potential (ζ), scanning electron microscopy (SEM), and transmission electron microscopy (TEM). The study was also extended to include silver nanoparticles (AgNPs) and gold nanoparticles (AuNPs) to evaluate broad-range applicability. Among the ligands studied, HPC functionalization demonstrated the widest range of phase-transfer stability across 21 days for all three particle systems studied. UV-vis spectroscopy demonstrated sustained LSPR integrity after HPC functionalization in EG, THF, and DCM. SEM, TEM, and hydrodynamic size measurements by DLS further confirmed no aggregation in EG, THF, and DCM but suggested possible twinning or clustering in the solution. Overall, this work successfully identified non-toxic alternatives to expand the LSPR stability of citrate-synthesized metal nanoparticles in organic solvents.

Indexed as

colloidal stabilitygold nanoparticlesgold–silver nanoshellslocalized surface plasmon resonancephase-transfersilver nanoparticles

Identifiers

PMID41304090
PMCPMC12654536

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Registered trials

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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.