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Surface modification

About: Surface modification is a research topic. Over the lifetime, 35544 publications have been published within this topic receiving 859567 citations.


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Journal ArticleDOI
Fu Zhang1, En-Tang Kang1, Koon Gee Neoh1, Peng Wang1, K.L. Tan1 
TL;DR: The PEGMA graft-polymerized stainless-steel coupon (PEGMA-g-SCA-SS) with a high graft concentration, and thus a high PEG content, was found to be very effective in preventing bovine serum albumin and gamma-globulin adsorption.

195 citations

Journal ArticleDOI
16 Oct 2003-Langmuir
TL;DR: In this paper, a simple surface modification technique was developed to functionalize polymeric and cellulosic materials with bactericidal polycationic groups, such as pyridinium groups.
Abstract: A simple surface modification technique was developed to functionalize polymeric and cellulosic materials with bactericidal polycationic groups. The poly(ethylene terephthalate) (PET) film was first graft copolymerized with 4-vinylpyridine (4VP) and subsequently derivatized with hexyl bromide via the quaternization of the grafted pyridine groups into pyridinium groups. The amount of pyridinium groups on the film surface could be controlled by varying the 4VP monomer concentrations used for grafting. The pyridinium groups introduced on the surface of the substrate possess antibacterial properties, as shown by their effect on Escherichia coli (E. coli). The bacteria killing efficiency is very high when the concentration of pyridinium groups on surfaces is 15 nmol/cm2 or higher. E. coli adhered on the functionalized surfaces are no longer viable when released into an aqueous culture medium. Filter paper, as a typical cellulosic material, was also functionalized in the same manner to introduce the pyridinium ...

195 citations

Journal ArticleDOI
Anke Krueger1, Jochen Stegk1, Yuejiang Liang1, Li Lu1, Gerald Jarre1 
01 Mar 2008-Langmuir
TL;DR: A simple and efficient method for the covalent functionalization of detonation nanodiamond is developed, which opens the way to covalently bonded diamond bioconjugates for labeling, drug delivery, and other applications.
Abstract: We have developed a simple and efficient method for the covalent functionalization of detonation nanodiamond. After homogenization of the surface by borane reduction, the surface was modified with (3-aminopropyl)trimethoxysilane. Subsequent grafting of biotin yielded covalently biotinylated nanodiamond, which was characterized by FTIR spectroscopy, X-ray powder diffractometry, thermogravimetry, and elemental analysis. The activity was tested with horseradish peroxidase-labeled streptavidin. The surface loading of biotin was found to be 1.45 mmol g-1. The new material opens the way to covalently bonded diamond bioconjugates for labeling, drug delivery, and other applications.

195 citations

Journal ArticleDOI
TL;DR: This procedure was done to enhance hole injection in an electronic device and involves sequential formation of a monolayer of a pi-conjugated organic semiconductor on the indium tin oxide (ITO) surface followed by doping with a strong electron acceptor.
Abstract: A new method is described for surface modification of ITO with an electroactive organic monolayer. This procedure was done to enhance hole injection in an electronic device and involves sequential formation of a monolayer of a π-conjugated organic semiconductor on the indium tin oxide (ITO) surface followed by doping with a strong electron acceptor. The semiconductor monolayer is covalently bound to the ITO, which ensures strong adhesion and interface stability; reduction of the hole injection barrier in these devices is accomplished by formation of a charge-transfer complex by doping within the monolayer. This gives rise to very high current densities in simple single layer devices and double layer light emitting devices compared to those with untreated ITO anodes.

194 citations

Journal ArticleDOI
TL;DR: The design and protocols of the two approaches to perfluorophenylazides (PFPA) coupling agents are reviewed, providing examples in which PFPA derivatives were successfully used in material surface functionalization, ligand conjugation, and the synthesis of hybrid nanomaterials.
Abstract: A major challenge in materials science is the ongoing search for coupling agents that are readily synthesized, capable of versatile chemistry, able to easily functionalize materials and surfaces, and efficient in covalently linking organic and inorganic entities. A decade ago, we began a research program investigating perfluorophenylazides (PFPA) as the coupling agents in surface functionalization and nanomaterial synthesis. The p-substituted PFPAs are attractive heterobifunctional coupling agents because of their two distinct and synthetically distinguishable reactive centers: (i) the fluorinated phenylazide, which is capable of forming stable covalent adducts, and (ii) the functional group R, which can be tailored through synthesis. Two approaches have been undertaken for material synthesis and surface functionalization. The first method involves synthesizing PFPA bearing the first molecule or material with a functional linker R and then attaching the resulting PFPA to the second material by activating the azido group. In the second approach, the material surface is first functionalized with PFPA via functional center R, and coupling of the second molecule or material is achieved with the surface azido groups. In this Account, we review the design and protocols of the two approaches, providing examples in which PFPA derivatives were successfully used in material surface functionalization, ligand conjugation, and the synthesis of hybrid nanomaterials. The methods developed have proved to be general and versatile, and they are applicable to a wide range of materials (especially those that lack reactive functional groups or are difficult to derivatize) and to various substrates of polymers, oxides, carbon materials, and metal films. The coupling chemistry can be initiated by light, heat, and electrons. Patterned structures can be generated by selectively activating the areas of interest. Furthermore, the process is easy to perform, and light activation occurs in minutes, greatly facilitating the efficiency of the reaction. PFPAs indeed demonstrate many benefits as versatile surface coupling agents and offer opportunities for further exploration.

194 citations


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Performance
Metrics
No. of papers in the topic in previous years
YearPapers
20232,530
20225,209
20211,961
20202,217
20192,313
20182,263