342 research outputs found
From Filter Paper to Functional Actuator by Poly(ionic liquid)-Modified Graphene Oxide
A commercially available membrane filter paper composed of mixed cellulose
esters bearing typically an interconnected pore structure was transformed into
a stimuli-responsive bilayer actuator by depositing a thin film of poly(ionic
liquid)-modified graphene oxide sheets (GO-PIL) onto the filter paper. In
acetone vapor, the as-synthesized bilayer actuator bent readily into multiple
loops at a fast speed with the GO-PIL top film inwards. Upon pulling back into
air the actuator recovered their original shape. The asymmetric swelling of the
top GO-PIL film and the bottom porous filter paper towards organic vapor offers
a favorably synergetic function to drive the actuation. The PIL polymer chains
in the hybrid film were proven crucial to enhance the adhesion strength between
the GO sheets and the adjacent filter paper to avoid interfacial delamination
and thus improve force transfer. The overall construction allows a prolonged
lifetime of the bilayer actuator under constant operation, especially when
compared to that of the GO/filter paper bilayer actuator without PIL.Comment: 23 pages, 7 figure
Plants to Polyelectrolytes: Theophylline Polymers and their Microsphere Synthesis
To extend fossil oil supplies, sustainable feed stocks for the production of
useful reagents and polymers should be harnessed. In this regard, chemicals
derived from plants are excellent candidates. While the vast majority of plant
sources used for polymer science only contain CxHyOz, alkaloids such as
caffeine, nicotine, and theophylline possess nitrogen functionality that can
provide new functions for bio-derived polymers and their synthesis. In this
context, we exploited the chemistry of theophylline, a natural product found in
chocolate and tea, to create a cationic poly(theophylline) in a straightforward
fashion for the first time. We demonstrate how this new polymer can be
synthesized and used for the creation of narrowly disperse cationic
microspheres.Comment: 19 pages, 13 figure
Nanoporous ionic organic networks: from synthesis to materials applications
The past decade has witnessed the rapid progress in synthesizing nanoporous
organic networks or polymer frameworks for various potential applications.
Generally speaking, functionalization of porous networks to add extra
properties and enhance materials performance could be achieved either during
the pore formation (thus a concurrent approach) or post-synthetic modification
(a sequential approach). Nanoporous organic networks which include ion pairs in
a covalent manner are of special importance and possess extreme application
profiles. Within these nanoporous ionic organic networks (NIONs), here with a
pore size in the range from sub-1 nm to 100 nm, we observe a synergistic
coupling of the electrostatic interaction of charges, the nanoconfinement
within pores and the addressable functional units in soft matter resulting in a
wide variety of functions and applications, above all catalysis, energy storage
and conversion, as well as environmental operations. This review aims to
highlight the recent progress in this area, and seeks to raise original
perspectives that will stimulate future advancements at both the fundamental
and applied level.Comment: 67 pages, 25 figures, Chemical Society Reviewers, 201
Grafting polymers onto carbon nitride via visible-light-induced photofunctionalization
Metal-free graphitic carbon nitride (g-CN) has attracted significant attention recently due to its multiple applications, such as photocatalysis, energy storage and conversion, and biomaterials, albeit formation of g-CN films is challenging. Herein, a “grafting to” route to graft polymer brushes onto g-CN via visible-light irradiation is described. Afterward, g-CN/polymer films can be obtained through spin coating on glass substrates. As such, the present material provides an improved process toward further application of g-CN in thin films. Moreover, an improved dispersibility in organic solvent was realized after grafting and functional groups (such as epoxides) were introduced to g-CN. Subsequently, the epoxy groups were utilized for further functionalization to adjust the surface polarity
Facile synthesis of new, highly efficient SnO2/carbon nitride composite photocatalysts for the hydrogen evolution reaction
Novel SnO2/carbon nitride photocatalysts having surface areas up to 220 m(2) g(-1) were prepared for the first time by condensation of dicyandiamide in alkali metal chloride/SnCl2-containing salt melts at 550 degrees C, without the use of hard templates. XRD and HR-TEM investigations showed that the obtained materials are composed of 5-10 nm SnO2 nanoparticles deposited onto nanosheets set up from 1D-melon ribbons. The morphology and crystalline structure of products appear to be greatly dependent on the synthesis temperature. SnO2/carbon nitride composites are found to be highly efficient in the photocatalytic reactions, as exemplified by Rhodamine B degradation and water reduction using Pt as a cocatalyst. Under the optimized synthesis conditions, these composite photocatalysts achieve hydrogen evolution rates more than 2 times higher than the mesoporous carbon nitride (mp-CN) under visible light irradiation. In principle, this new method based on utilization of MCl/SnCl2 salt melts as a reaction medium allows carrying out various polymerization reactions in the presence of the mild Lewis acid in the solution phase in the wide temperature range of 180-550 degrees C. Moreover, SnCl2 eutectics are even suitable for post-synthesis modification of the bulk carbon nitride to tune its morphology and greatly increase the surface area and photocatalytic activity
Main-chain Polyimidazolium Polymers by One-pot Synthesis and Application as Nitrogen-doped Carbon Precursors
This paper reports on the one-pot synthesis of main-chain
imidazolium-containing polymers, some of which show unusually high thermal
stability. The imidazolium polymers were obtained by modified
Debus-Radziszewski reactions for the chain build-up from simple organic
compounds, here pyruvaldehyde, formaldehyde, acetic acid, and a variety of
diamines. The reactions were performed in aqueous media at ambient conditions,
being synthetically elegant, convenient and highly efficient. Finally, a simple
anion-metathesis reaction was conducted to replace the acetate anion with
dicyanamide, and the thermal properties of the main-chain polyimidazoliums
before and after anion exchange were studied in detail, which demonstrated
chain cross-linking by the counterion and a coupled unusually high
carbonization yield of up to 66 wt% at 900 oC.Comment: 17 pages, 13 figure
Carbon nitride thin films as all-in-one technology for photocatalysis
Organic π-conjugated polymers are promising heterogeneous photocatalysts that involve photoredox or energy transfer processes. In such settings, the materials are usually applied in the form of dis..
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Capacitive deionization using biomass-based microporous salt-templated heteroatom-doped carbons
Microporous carbons are an interesting material for electrochemical applications. In this study, we evaluate several such carbons without/with N or S doping with regard to capacitive deionization. For this purpose, we extent the salt-templating synthesis towards biomass precursors and S-doped microporous carbons. The sample with the largest specific surface area (2830 m2 g−1) showed 1.0 wt % N and exhibited a high salt-sorption capacity of 15.0 mg g−1 at 1.2 V in 5 mM aqueous NaCl. While being a promising material from an equilibrium performance point of view, our study also gives first insights to practical limitations of heteroatom-doped carbon materials. We show that high heteroatom content may be associated with a low charge efficiency. The latter is a key parameter for capacitive deionization and is defined as the ratio between the amounts of removed salt molecules and electrical charge
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