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@MASTERSTHESIS{Jidar:1043492,
author = {Jidar, Rihab},
title = {{S}elf-assembly of {S}ilica {N}anospheres into
{W}ell-{O}rdered {S}tructures via {A}nnealing},
school = {FH Aachen},
type = {Bachelorarbeit},
reportid = {FZJ-2025-02886},
pages = {41 p.},
year = {2025},
note = {Bachelorarbeit, FH Aachen, 2025},
abstract = {The structural properties of nanoparticles have attracted
significant interest due to their potentialapplications in
various fields such as catalysis, drug delivery, and optics
[1]. Their nanoscaledimensions and large surface area to
volume ratio provide unique characteristics, includinghigher
reactivity, selectivity, and mechanical strength compared to
bulk materials. Among them,silica nanoparticles (SiO₂ NPs)
are particularly interesting because of their chemical
stability,biocompatibility, and ease of surface
functionalization[2].Controlled self-assembly of silica
nanoparticles into well-ordered structures is essential
foroptimizing their functional performance in advanced
applications. Self-assembled monolayers(SAMs) of silica
nanoparticles offer a promising route to achieve such
organization. The successof this process is strongly
influenced by temperature, which affects key factors like
solventevaporation rate and particle mobility. Techniques
such as spin-coating and drop-casting exploitthese thermally
dependent behaviors to achieve desired nanoparticle
arrangements. Therefore,understanding and regulating
temperature effects is critical for improving the uniformity
andquality of self-assembled nanostructures [3].Several
studies have explored how thermal treatment (annealing) can
be used to improve theorder and stability of nanoparticle
assemblies. For example, Jiang et al. (2003) demonstrated
thatpost-deposition thermal annealing enhances particle
mobility, allowing silica nanospheres torearrange into more
ordered hexagonal arrays[4]. Similarly, Zhang et al. (2010)
reported thatannealing promotes defect healing in monolayers
formed via drop-casting, especially attemperatures near the
glass transition of added organic agents [5]. Annealing has
also been usedin combination with surface tension gradients
or capillary forces to refine large-area colloidalcrystal
films with fewer voids and grain boundaries [6]. These
studies highlight the importanceof optimizing thermal
parameters to promote self-organization and reduce
structural defects.However, the key question that this study
aims to address is to determine whether shorterannealing
durations at elevated temperatures can yield a level of
ordering that is comparable towhat was previously achieved
in earlier studies—such as the work by Qdemat et al.[7],
where awell-ordered silica nanoparticle monolayer was
obtained after annealing at 70 °C for 10 days.This
comparison is important because it explores whether thermal
energy at higher temperaturescan accelerate the ordering
process, potentially reducing the required treatment time.
Therationale behind this investigation is that nanoparticle
self-assembly is influenced by bothtemperature and time, and
optimizing this balance could allow for more efficient film
formationwithout compromising structural quality.This study
investigates the self-assembly behavior of silica
nanoparticles approximately 200 nmin diameter on silicon
substrates using the drop-casting method, with a particular
focus on therole of annealing temperature. By systematically
varying the thermal conditions andcharacterizing the
resulting structures using Scanning Electron Microscopy
(SEM), we aim toevaluate how temperature influences particle
organization and contributes to the formation ofhighly
ordered monolayers. The findings aim to clarify whether more
time-efficient thermaltreatments can still achieve
high-quality ordering, which could inform future
experimental designand practical applications in
nanofabrication.},
cin = {JCNS-2 / JARA-FIT},
cid = {I:(DE-Juel1)JCNS-2-20110106 / $I:(DE-82)080009_20140620$},
pnm = {632 - Materials – Quantum, Complex and Functional
Materials (POF4-632) / 6G4 - Jülich Centre for Neutron
Research (JCNS) (FZJ) (POF4-6G4)},
pid = {G:(DE-HGF)POF4-632 / G:(DE-HGF)POF4-6G4},
typ = {PUB:(DE-HGF)2},
doi = {10.34734/FZJ-2025-02886},
url = {https://juser.fz-juelich.de/record/1043492},
}