The generation of polymer brushes by surface-initiated controlled radical polymerization (SI-CRP) techniques has become a powerful approach to tailor the chemical and physical properties of interfaces and has given rise to great advances in surface and interface engineering. Polymer brushes are defined as thin polymer films in which the individual polymer chains are tethered by one chain end to a solid interface. Significant advances have been made over the past years in the field of polymer brushes. This includes novel developments in SI-CRP, as well as the emergence of novel applications such as catalysis, electronics, nanomaterial synthesis and biosensing. Additionally, polymer brushes prepared via SI-CRP have been utilized to modify the surface of novel substrates such as natural fibers, polymer nanofibers, mesoporous materials, graphene, viruses and protein nanoparticles. The last years have also seen exciting advances in the chemical and physical characterization of polymer brushes, as well as an ever increasing set of computational and simulation tools that allow understanding and predictions of these surface-grafted polymer architectures. The aim of this contribution is to provide a comprehensive review that critically assesses recent advances in the field and highlights the opportunities and challenges for future work.
The tribological properties, lubrication mechanism, characterization methods and potential applications of surface-attached polymer-based boundary lubricants are reviewed.
There is a need for coatings for biomedical devices and implants that can prevent the attachment of fungal pathogens while allowing human cells and tissue to appose without cytotoxicity. Here, the authors study whether a poly(2-hydroxyethylmethacrylate) (PHEMA) coating can suppress attachment and biofilm formation by Candida albicans and whether caspofungin terminally attached to surface-tethered polymeric linkers can provide additional benefits. The multistep coating scheme first involved the plasma polymerization of ethanol, followed by the attachment of α-bromoisobutyryl bromide (BiBB) onto surface hydroxyl groups of the plasma polymer layer. Polymer chains were grafted using surface initiated activators regenerated by electron transfer atom transfer radical polymerization with 2-hydroxyethylmethacrylate, yielding PHEMA layers with a dry thickness of up to 89 nm in 2 h. Hydroxyl groups of PHEMA were oxidized to aldehydes using the Albright-Goldman reaction, and caspofungin was covalently immobilized onto them using reductive amination. While the PHEMA layer by itself reduced the growth of C. albicans biofilms by log 1.4, the addition of caspofungin resulted in a marked further reduction by >4 log units to below the threshold of the test. The authors have confirmed that the predominant mechanism of action is caused by antifungal drug molecules that are covalently attached to the surface, rather than out-diffusing from the coating. The authors confirm the selectivity of surface-attached caspofungin in eliminating fungal, not mammalian cells by showing no measurable toxicity toward the myeloid leukaemia suspension cell line KG-1a.
The introduction of interchain cross-links in surface-grafted polymer brushes increases the robustness and mechanical properties of these thin polymer films. In most cases, cross-linked polymer brushes contain permanent interchain cross-links. The use of reversible interchain cross-links, in contrast, provides opportunities to dynamically modulate the cross-link density and properties of surface-grafted polymer brushes. This study explores the use of disulfide bonds to reversibly cross-link poly(2-(dimethylamino)ethyl methacrylate) copolymer brushes. These brushes were prepared via surface-initiated atom transfer radical copolymerization of 2-(dimethylamino)ethyl methacrylate and an azide-containing comonomer, 3-azido-2-hydroxypropyl methacrylate, followed by copper(I)-catalyzed azide−alkyne cycloaddition of S-propargyl thioacetate and subsequent deprotection of the thioacetate moieties. Heating the polymer brushes to 60 °C under air for 2 h resulted in the formation of disulfide cross-links, which could be reduced to generate the corresponding free thiol groups upon brief exposure to tris(2-carboxyethyl)phosphine hydrochloride. The formation and cleavage of the interchain disulfide cross-links has a profound influence on the swelling and viscoelastic properties of the brushes. Cross-linking leads to a decrease in swelling ratio and a concomitant dehydration and loss in dissipative properties of the brush film. These changes were observed using ellipsometry and quartz crystal microbalance with dissipation monitoring experiments by exposing the polymer brushes to a sequence of successive cross-linking and uncross-linking steps. These experiments indicated that while cross-linking and uncross-linking were fully reversible during the first few cycles, the response of the brush films became less pronounced upon prolonged oxidation/reduction, which was attributed to the oxidation of thiol side-chain functional groups and a concomitant reduction in the cross-link density of the polymer brushes. The results presented in this study show that the incorporation of disulfide interchain cross-links allows access to polymer brush films that can be reversibly cross-linked and uncrosslinked over many cycles.
Earth-abundant hydrogen evolution catalysts are essential for high-efficiency solar-driven water splitting. Although a significant amount of studies have been dedicated to the development of new catalytic materials, the microscopic assembly of these materials has not been widely investigated. Here, we describe an approach to control the three-dimensional (3D) assembly of amorphous molybdenum sulfide using polymer brushes as a template. To this end, poly(dimethylaminoethyl methacrylate) brushes were grown from highly oriented pyrolytic graphite. These cationic polymer films bind anionic MoS through an anion-exchange reaction. In a final oxidation step, the polymer-bound MoS is converted into the amorphous MoS catalyst. The flexibility of the assembly design allowed systematic optimization of the 3D catalyst. The best system exhibited turnover frequencies up to 1.3 and 4.9 s at overpotentials of 200 and 250 mV, respectively. This turnover frequency stands out among various molybdenum sulfide catalysts. The work demonstrates a novel strategy to control the assembly of hydrogen evolution reaction catalysts.
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.