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Flexible HVO paper as cathode for Li-ion batteries

Could rechargeable batteries for portable electronic devices be flexible and rollable?

Scientists in Singapore show that hydrated vanadium pentoxide (HVO)-based bulky paper are excellent candidates for cathodes in lithium ion batteries. Paper is lightweight, low-cost and flexible and provide many advantages over carbon nanotubes and graphene nanosheets.

The team led by Tuti Mariana Lim and Qingyu Yan, Nanyang Technological University, Singapore prepared bulky paper from HVO nanobelts, which they synthesised using a very efficient hydrothermal method (up to 99% yield). The nanobelts were several micrometers long, ~20nm in diameter and ~10nm in thickness. Flexible bulky-paper cathodes were made without the addition of binders.

“These flexible electrodes show high reversible Li storage capacities, good high C-rate performance with ~100% coulombic efficiency,” claim Lim and Yu.

“These promising properties of binder-free flexible electrodes can be an important step for development of rollable rechargeable battery with desired energy storage performance.”

Read the full paper for free upon a simple registration process:

Facile preparation of hydrated vanadium pentoxide nanobelts based bulky paper as flexible binder-free cathodes for high-performance lithium ion batteries

Xianhong Rui, Jixin Zhu, Weiling Liu, Huiteng Tan, Daohao Sim, Chen Xu, Hua Zhang, Jan Ma, Huey Hoon Hng, Tuti Mariana Lim and Qingyu Yan
RSC Adv., 2011, 1, 117-122

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PVA excellent for solar cell encapsulation

French scientists explain how polyvinyl alcohol (PVA) is an excellent oxygen-barrier polymer for solar cell encapsulation. The team led by Jean-Luc Gardette, at the University of Clermont, conducted photochemical studies of PVA under solar light. They showed that the photooxidative degradation of PVA are restricted to the first 5 micron at the surface of the exposed films. The researchers also identified the low molecular weight products such as carboxylic acids that can be trapped in the film or migrate in the gas phase and they proposed an oxidative mechanism to account for these modifications.

However, the most appealing property of PVA is its “high stability upon irradiation in the absence of oxygen, even after long exposure in conditions of accelerated ageing”, says Gardette.  Indeed, PVA is an excellent candidate for  the multilayer encapsulation system of Organic Solar Cells (OSCs) due to its high durability, “as long as the PVA layer is protected from
air by an inorganic layer as a first outside layer in the inorganic/organic multistack”.

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Photochemical behavior of PVA as an oxygen-barrier polymer for solar cell encapsulation
Julien Gaume, Pascal Wong-Wah-Chung, Agnès Rivaton, Sandrine Thérias and Jean-Luc Gardette
RSC Adv., 2011, Advance Article, DOI: 10.1039/C1RA00350J

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Detecting vancomycin-resistant bug with DNA sensor

Scientists in China have improved the accuracy of DNA sensors for use in disease detection. 

DNA sensors detect pathogenic and genetic diseases by binding to target DNA strands that are related to the disease and giving a signal that shows how much of the DNA is present. Recent developments in the technology make use of gold nanoparticles functionalised with primer strands that bind to the DNA of interest. When the primers link to the targets, changes in the nanoparticles’ UV-visible absorbance provide a quantifiable signal. 

Ken Cham-Fai Leung from the Chinese University of Hong Kong and coworkers have modified this approach to improve the sensitivity and accuracy. 

Sensors employing gold nanoparticles randomly functionalised with single-stranded primer DNA can lead to primer strand cross-binding, resulting in agglomeration. This can entrap the nanoparticles and reduce the number of primer strands available for binding to the target DNA, leading to inaccurate changes in absorbance signals. 

Primer strands attached to a gold nanoparticle

The monofunctionalised nanoparticles form discrete nanostructures (left), whilst randomly functionalised nanoparticles tend to aggregate (right)

To combat this problem, Leung  and his team made monofunctionalised gold nanoparticles to which just one primer strand complementary to the target DNA was attached. The team used the nanoparticles to detect a DNA strand just 10 bases long, related to Enterococcus faecalis, a bacterium that can cause life-threatening infections. The shorter primer strands then needed to attach to the nanoparticles displayed reduced steric and electrostatic repulsions, decreasing the tendency for agglomeration. ‘Using these structurally well-defined, monofunctionalised gold nanoparticles will provide more quantitative results for DNA detection,’ says Leung. 

The nanoparticle complexes are soluble in organic solvent mixtures in which longer DNA sequences are typically denatured; using such solvents could provide novel approaches for gene delivery. 

‘The work has enriched our current understanding of DNA hybridisation in organic media, and it clearly shows good potential for future applications in biomedical research and new sensor developments,’ says Cong Yu, an expert in nucleic acid chemistry from the Changchun Institute of Applied Chemistry, China.   

Sarah Farley 

The above story was published in Chemistry World on the 7th October 2011: Detecting diseases with DNA sensors

The full article is free to download after a simple registration process:

DNA hybridization of pathogenicity island of vancomycin-resistant Enterococcus faecalis with discretely functionalized gold nanoparticles in organic solvent mixtures
Chun-Pong Chak, Josie M. Y. Lai, Kathy W. Y. Sham, Christopher H. K. Cheng and Ken Cham-Fai Leung, RSC Adv., 2011
DOI:10.1039/c1ra00304f, Advanced Article

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Understanding explosives for safe manufacture

RDX (hexahydro-1,3,5-trinitro-s-triazine) is a rocket propellant but its manufacture comes with high risk of explosion.

Ke-Li Han from the Dalian Institute of Chemical Physics, China, and colleagues have used a computational study to gauge which parts of the synthesis of the RDX precursor TRAT (hexahydro-1,3,5-triacetyl-s-triazine) are most likely to cause an explosion.

They found that of the four stages in the synthesis – imine formation, amino methylation, dehydration and trimerisation – the second and fourth stages are the most likely to release energy in the form of an explosion. The team suggests that more attention is paid to these stages of production.

The full article is free to access upon a simple registration process.

A reaction of formaldehyde with acetonitrile: understanding the preparation of RDX (I), X-F Chen, B-Z Wang and K-L Han, RSC Adv., 2011, DOI: 10.1039/c1ra00239b

 

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Graphene: electrochemically not so wonderful

The Chemistry World team reports on a recently published RSC Advances article on the use of graphene in electrochemistry – “wonder material not so wonderful“. 

Graphene – a sheet of graphite just one atom thick – is often claimed to be a wonder material, thanks to its superlative mechanical, thermal and electrical properties. But now a group of UK chemists is claiming that, in an electrochemical setting, graphene is not such a wonder material after all. Contrary to the widely held view, the chemists think graphene electrodes are mostly ineffective at transferring electrons, implying that graphene is a poor choice for sensing applications.

Craig Banks and others at Manchester Metropolitan University came to the conclusion after having performed electrochemical experiments with various electrodes. Some of these electrodes were coated in a single graphene layer, some were coated in a graphene multi-layer, and some were left uncovered. Carefully measuring the current passing through the electrodes while changing the applied voltage, Banks’s group discovered that electron transfer in graphene occurs mostly around its edges and at any defects. ‘Given its geometric size, this means that it is largely unreactive,’ says Banks.

Graphene

Chemists think that graphene electrodes are mostly ineffective at transferring electrons, implying that graphene is a poor choice for sensing applications

The chemists believe that graphene researchers generally modify electrodes in one of two ways: coating them with a single layer of graphene, which tends to block electron transfer, and coating them with a graphene multi-layer, which sometimes improves electron transfer. However, multi-layered graphene is more akin to graphite, say Banks’s group, and has more edges to supply electrons. What’s more, different underlying electrodes can have different responses to graphene coating. ‘Researchers in the field need to be more informed and consider that the electrode they are modifying is critical as well as the coverage of graphene,’ says Banks. 

Alexander Balandin, a materials scientist specialising in graphene at the University of California at Riverside, US, thinks the results are important, and agrees that graphene coatings should be compared with graphite coatings in future electrochemical experiments. ‘At the same time, I would not jump too quickly to the conclusions and rule out graphene as the electrode material completely,’ he says. ‘It is known that depending on the graphene quality, exact number of the atomic planes, environment and functionalisation of its surface, graphene’s properties can vary a lot.’ 

In fact, for many applications graphene may still be a wonder material. The results of Banks’s group do not necessarily affect graphene’s potential uses as a transparent conductor for touch screens or as a heat sink, for example. And Banks points out that slow electron transfer in electrochemistry is sometimes an advantage. ‘Graphene [still] has huge potential in energy storage and generation applications,’ he says. 

Jon Cartwright

The full article is free to access upon a simple registration process:

Electrochemistry of graphene: not such a beneficial electrode material?
Dale A. C. Brownson, Lindsey J. Munro, Dimitrios K. Kampouris and Craig E. Banks, RSC Adv., 2011, Advance Article, DOI: 10.1039/c1ra00393c

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Hydrogenation reactions in micelles

Can hydrogenation reactions be performed in water? German scientists say: “Yes we can!”

Often, water is seen as the “green solvent” of choice as it is non-flammable and non-toxic. However, organic chemists usually face issues with the solubility of the reactants in water. In this RSC Advances article, Schwarze et al. demonstrate the power of the surfactants in a hydrogenation reaction of prochical C–C, double bonds in itaconate, e.g. dimethyl itaconate.

The selectivity were comparable to when the same reaction were performed in methanol. The reaction rates however were slightly slower. This was due to the lower hydrogen solubility in the micellar aqueous systems. But the beauty of the reaction is that no notable catalyst deactivation occurred and the latter was recyclable with a turn-over number of >1000 in the aqueous micellar conditions .

In this publication, the authors also developed a model to predict the performance of micellar reaction systems. The partition coefficient of the substrates between the micelles and the continuous aqueous phase can be predicted using the Conductor-like Screening Model for Real Solvents (COSMO-RS).

If you want to find out more about this work, please read the full paper here*.

Rhodium catalyzed hydrogenation reactions in aqueous micellar systems as green solvents
M. Schwarze, J.S. Milano-Brusco, V. Strempel, T. Hamerla, S. Wille, C. Fischer, W. Baumann, W. Arlt and R. Schomäcker
RSC Adv., 2011, DOI: 10.1039/C1RA00397F, Advance Article

*Individuals can access the content by signing up for an RSC Publishing Personal Account. Existing institutional RSC journal subscribers, with registered IP, have automatic access. Other institutions can register for free access.

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