Layer-by-layer assembly of charged particles in nonpolar media.

Langmuir

Department of Chemical and Biomolecular Engineering, University of Pennsylvania, Philadelphia, Pennsylvania 19104, USA.

Published: June 2010

Layer-by-layer (LbL) assembly of charged species such as nanoparticles and polymers has been widely used to generate functional thin films with unique wetting, optical, catalytic, and biological properties. Although LbL assembly is a versatile tool for creating functional thin films on a variety of substrates, it is generally restricted to aqueous media, in which electrolytes ionize readily due to the large dielectric constant of water. LbL assembly of non-water-soluble materials would expand the range of film properties and functionalities that are attainable. In this study, we have successfully performed LbL deposition of charged particles in a nonpolar solvent, toluene. In toluene, carbon black (CB) and alumina acquired negative and positive surface charge, respectively, in the presence of a charge-inducing agent, Aerosol OT (AOT). The dependence of particle surface charge on the concentration of AOT in toluene was probed by electrophoretic mobility analysis. The two oppositely charged particles were sequentially deposited onto glass slides to form CB/Al(2)O(3) nanocomposite thin films. UV-vis spectroscopy, optical profilometry, and thermogravimetric analysis (TGA) were used to investigate the effect of assembly conditions (i.e., the concentration of AOT in each suspension) on the composition and growth behavior of CB/Al(2)O(3) nanocomposite films. Our results demonstrate that LbL assembly can indeed be performed using charged particles in nonpolar media. Such possibility will widen the library of materials that can be incorporated into thin films based on the LbL technique, which can ultimately lead to the generation of multifunctional nanocomposite thin films.

Download full-text PDF

Source
http://dx.doi.org/10.1021/la1000655DOI Listing

Publication Analysis

Top Keywords

thin films
20
charged particles
16
lbl assembly
16
particles nonpolar
12
assembly charged
8
nonpolar media
8
functional thin
8
surface charge
8
concentration aot
8
cb/al2o3 nanocomposite
8

Similar Publications

High Performance of Cs2AgBiBr6 Perovskite-based Photodetectors by Adding DEAC.

Chemistry

December 2024

East China University of Science and Technology, School of Materials Science and Engineering, meilong Road, 200237, shanghai, CHINA.

Perovskite-based photodetectors (PDs) are broadly utilized in optical communication, non-destructive testing, and smart wearable devices due to their ability to convert light into electrical signals. However, toxicity and instability hold back their mass production and commercialization. The lead-free Cs2AgBiBr6 double perovskite film, promised to be an alternative, is fabricated by electrophoretic deposition (EPD), which compromises film quality.

View Article and Find Full Text PDF

High photothermal conversion efficiency of RF sputtered TiO Magneli phase thin films and its linear correlation with light absorption capacity.

Sci Rep

December 2024

Centre Énergie, Matériaux Télécommunications, Institut National de la Recherche Scientifique, 1650, Blvd, Lionel-Boulet, Varennes, QC, J3X-1P7, Canada.

RF-sputtering is used to deposit TiO-Magneli-phase films onto various substrates at deposition temperatures (T) ranging from 25 to 650 °C. Not only the structural, but also electrical conductivity, optical absorbance and photothermal properties of the TiO films are shown to change significantly with T. A T of 500 °C is pointed out as the optimal temperature that yields highly-crystalized pure-TiO-Magneli phase with a densely-packed morphology and a conductivity as high as 740 S/cm.

View Article and Find Full Text PDF

Due to their outstanding electrical and thermal properties, graphene and related materials have been proposed as ideal candidates for the development of lightweight systems for thermoelectric applications. Recently, the nanolaminate architecture that entails alternation of continuous graphene monolayers and ultrathin polymer films has been proposed as an efficient route for the development of composites with impressive physicochemical properties. In this work, we present a novel layer-by-layer approach for the fabrication of highly ordered, flexible, heat-resistant, and electrically conductive freestanding graphene/polymer nanolaminates through alternating Marangoni-driven self-assembly of reduced graphene oxide (rGO) and poly(ether imide) (PEI) films.

View Article and Find Full Text PDF

Robust and ultra-thin nanocellulose/MXene composite film and its performance in efficient electricity-generation and sensing.

Int J Biol Macromol

December 2024

Department of Plastic and Cosmetic Surgery, Treatment Center of Burn and Trauma, Affiliated Hospital of Jiangnan University, Wuxi 214122, China. Electronic address:

The conversion of mechanical energy into electrical energy by triboelectric nanogenerators (TENG) has attracted attention in recent years, particularly in the field of wearable sensor. In this work, TEMPO-oxidized cellulose nanofibers (TOCNF) with carboxylate groups were compounded with MXene to serve as both the negative friction layer and the electrode in assembling a TENG with nylon. The synergistic effect between TOCNF and MXene was analyzed to disclose its influence on the performance of the as-prepared TENG.

View Article and Find Full Text PDF

In this study, we have investigated the surface-enhanced Raman scattering (SERS) spectra of myoglobin on silver substrates with different morphology. The aim was to determine the optimal parameters of analyte and substrate preparation for obtaining of high-amplitude SERS spectra of proteins. It is shown that not only the morphology of the silver film, but also the method of analyte molecules deposition on the SERS substrate plays an important role.

View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!