Archive for the ‘Hot Article’ Category

An electric partnership

Researchers in the US have uncovered an intriguing electrochemical partnership between two bacteria, which boosts their combined ability to generate an electric current when they are grown in a bioelectrochemical reactor. The work could lead to more efficient reactors, as well as throwing light on the ecological relationship between microbes in the wider environment.

Certain microbes can metabolise organic waste in a way that releases electrons, which can be transferred to an electrode and used to generate electric power or in electrochemical reactions to make useful products. One common bacterium that has been investigated in such bioelectrochemical systems is Pseudomonas aeruginosa.  In some natural environments, such as marine sediments, P. aeruginosa is found to be associated with another microbe, Enterobacter aerogenes. On the face of things, such a partnership appears unlikely as each bacterium has apparently different metabolic preferences. Now, a team led by Lars Angenent at Cornell University, Ithaca, has shown why these organisms can live in harmony in an energetically efficient way.

‘We found that when you feed a sugar such as sucrose to the mixed colony, this is fermented by E. aerogenes and one of the fermentation products is 2,3-butanediol,’ says Angenent. ‘This in turn is a substrate for P. aeruginosa. But not only does the alcohol act as a nutrient for Pseudomonas, it also stimulates it to produce redox mediators called phenazines.’

Bioelectrochemical systems with the bacteria P. aeruginosa with glucose (right) and 2,3-butanediol (left)

The current produced by a culture of P. aeruginosa with 2,3-butanediol (left) was increased two-fold compared with glucose (right) as the carbon source, owing to enhanced phenazine production

 

Phenazines are three-ringed nitrogen-containing compounds that can ‘traffic’ electrons. One particular phenazine that 2,3-butanediol stimulates P. aeruginosa to produce in excess is pyocyanin. This is used by E. aerogenes to increase its efficiency of metabolism of its sugar substrate from relatively inefficient fermentation to respiration, which generates electrons that can be fed into the electrode of the reactor.

The team found that when the two organisms are together, they produce 14 times more electric current than when on their own. Feeding a monoculture of P. aeruginosa with 2,3-butanediol results in a doubling of electric current, while exposing E. aerogenes to pyocyanin causes its current production to rise almost 20-fold. The study is the first to demonstrate metabolite based ‘inter-species communication’ in bioelectrochemical systems, resulting in enhanced electrochemical activity, says Angenent, adding: ‘It also explains how an inconsequential fermenter can become an important electrode-respiring bacterium within an ecological network at the anode.’

Korneel Rabaey, who works at the Advanced Water Management Centre at the University of Queensland in Australia, says: ‘As microbial populations will be essential for stable current generation, particularly when waste feedstocks are used as a fuel, understanding what drives high current output and stable community performance is an essential part in the development of this technology.’

Simon Hadlington

Link to journal article

Metabolite-based mutualism between Pseudomonas aeruginosa PA14 and Enterobacter aerogenes enhances current generation in bioelectrochemical systems
Arvind Venkataraman, Miriam A. Rosenbaum, Sarah D. Perkins, Jeffrey J. Werner and Largus T. AngenentEnergy Environ. Sci., 2011
DOI: 10.1039/c1ee01377g

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Hot article: Avoiding bubble formations in water splitting

A way to avoid bubble formation in photoelectrolysis systems – which split water into hydrogen and oxygen – so that water vapour can be electrolysed at room temperature at current densities in excess of those produced by the best photoelectrolysis systems has been developed by US scientists.

The formation of hydrogen through water electrolysis is one viable approach for solar fuel production on a global scale. Although photovoltaic modules can be connected to conventional electrolysers to split water, photoelectrolysis systems, in which sunlight is absorbed and the energy directly converted to decompose water to hydrogen and oxygen, have the potential to be more inexpensive and efficient.

An efficient photoelectrolyser, however, tends to limit its own performance by the formation of copious bubbles of gaseous products that inhibit the process by reflecting light and slowing the transfer of water to the catalyst reaction sites. Without concentrators, the intensity of the solar photon flux limits photoelectrolysers to far lower current densities than are used in conventional electrolysers.

Read this paper hot off the press! 

Reference:
J M Spurgeon and N S Lewis, Energy Environ. Sci., 2011
DOI: 10.1039/c1ee01203g

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Thermally self-sustained syngas generation

HOT article: A thermally self-sustained syngas generation on Rh-nanoparticles triggered by electric and chemical energy for micro-SOFC power plants:

A fast hybrid start-up process for thermally self-sustained catalytic n-butane reforming in micro-SOFC power plants
Alejandro J. Santis-Alvarez, Majid Nabavi, Nora Hild, Dimos Poulikakos and Wendelin J. Stark
Energy Environ. Sci., 2011, DOI: 10.1039/C1EE01330K

syngas

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A promising new fuel cell electrode design

Using known materials, scientists at the Georgia Institute of Technology in the USA have designed a new electrode architecture for solid oxide fuel cells (SOFCs) that overcomes many of the limitations of existing electrodes.

SOFCs are an exciting and promising source of power, which are able to provide clean and renewable energy and are scalable to suit a number of applications. They are essentially larger versions of batteries that have a solid electrolyte in which the charge carriers are oxide ions. Oxygen is introduced at the anode, which is reduced to oxide ions which then migrates across the solid electrolyte to the cathode. Fuel, such as hydrogen, is introduced at the cathode, which is oxidised by the oxide ions.

However, improvements to materials and components are still necessary, particularly for designing SOFCs that can operate at lower temperatures.

One of these challenges is to improve electrode design, which is expected to demonstrate fast ionic/electronic transport, rapid surface electrochemical reactions, chemical and physical compatibility with other components of the fuel cell (important considering fuel cells typically operate at many hundreds of degrees Celsius) and stability at high temperatures and oxidising environments.

Although La0.85Sr0.15MnOδ (LSM) and La0.6Sr0.4Co0.2Fe0.8O3−δ (LSCF) are commonly used cathode materials, they each have their limitations; LSM has poorer ionic conductivity and surface exchange kinetics than LSCF whilst LSCF has poor surface catalytic properties and also has inadequate longevity.

Meilin Liu and co-workers, however, have combined both materials in a new electrode architecture. Their design, which consists of a LSCF backbone coated with a thin-film of LSM, combines the materials’ desirable properties of high conductivity and excellent stability and catalytic activity, respectively.

This new architecture, the authors say, could be cheaply and easily applied to current commercial fuel cells and could also represent a net decrease in cell cost, due to the improvements in performance and stability.

Read more about this hot research here.

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Environmental behaviour of spent nuclear fuel

The world’s first spent nuclear fuel repository concept (Swedish KBS-3) has been illustrated by a team from Sweden.

The researchers looked at what happens when canisters containing spent fuel are breached at the early stages of disposal. In deoxygenated synthetic groundwater (2 mM NaHCO3), under radiation, leaching rates of fission products (137Cs, 90Sr and 99Tc) and actinides (238U, 237Np) from a spent fuel segment were found to be around 10-6 and 10-7 per day, respectively.

The team found that a cast-iron canister surface could immobilise 238U, 90Sr, 99Tc and 237Np dissolved from spent fuel, but a copper surface could not. In the presence of the oxidative species generated from water radiolysis, the corrosion rates of waste canister materials, copper and cast-iron were found to be 1 and 30 mm per year, respectively. The observation of insignificant dissolution of spent fuel in the leaching solution equilibrated with 0.1 atm H2 is explained by the reducing effects of H2 in the presence of fission-product alloy particles (Mo–Tc–Ru–Rh–Pd) as catalysts and dissolved Fe(II) in groundwater.

Reference:
Environmental behaviors of spent nuclear fuel and canister materials
D Cui, J Low and K Spahiu
Energy Environ. Sci., 2011, DOI: 10.1039/c0ee00582g

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Conversion of biomass-derived feedstocks using zeolite catalysts

biomass conversionEnergy & Environmental Science ‘HOT’ paperread it today!

This paper by Editorial Board member George Huber discusses the conversion of biomass-derived feedstocks into aromatics and olefins using zeolite catalysts. They show how it can be explained by the hydrogen to carbon effective (H/Ceff) ratios of the feeds.

Catalytic conversion of biomass-derived feedstocks into olefins and aromatics with ZSM-5: the hydrogen to carbon effective ratio
Huiyan Zhang, Yu-Ting Cheng, Tushar P. Vispute, Rui Xiao and George W. Huber
Energy Environ. Sci., 2011, DOI: 10.1039/C1EE01230D

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EES desalination paper featured on ACS Noteworthy Chemistry

An Energy & Environmental Science paper has featured today on ACS Noteworthy Chemistry – check it out today!

saltwaterVery low temperature membrane-free desalination by directional solvent extraction
Anurag Bajpayee, Tengfei Luo, Andrew Muto and Gang Chen
Energy Environ. Sci., 2011, 4, 1672-1675
DOI: 10.1039/C1EE01027A

This article was also featured in Chemistry World  – read the article:

Simple salt removal to get fresh water

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Photo-assisted water oxidation

US scientists have used a silicon photoanode substrate to process cobalt metal thin films to form a cobalt-based water oxidation catalyst (Co–Pi).

The Co–Pi loaded electrodes show significant improvement (x 100) over bare silicon photoanodes. Integrating chemical electrocatalysts for water splitting and photoanode materials to achieve light assisted water oxidation for the generation of solar fuels is a longstanding challenge.

The team’s results demonstrate the importance of material selection and device engineering to harness the solar spectrum towards catalytic chemical fuel production. The robust and abundant silicon electrode and direct processing of the cobalt metal produce an improved light assisted water oxidation device.

Reference:
Photo-assisted water oxidation with cobalt-based catalyst formed from thin-film cobalt metal on silicon photoanodes
Elizabeth R. Young, Ronny Costi, Sarah Paydavosi, Daniel G. Nocera and Vladimir Bulović
Energy Environ. Sci., 2011, DOI: 10.1039/C1EE01209F

Read it today!

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Solid-state hydrogen storage for mobile applications: Quo Vadis?

‘HOT’ off the press read this article now

Solid-state hydrogen storage approaches are reviewed and strategies for further improvement are discussed in this informative feature article…

Perspective article
Solid-state hydrogen storage for mobile applications: Quo Vadis?
Claudia Weidenthaler and Michael Felderhoff
Energy Environ. Sci., 2011, DOI: 10.1039/C0EE00771D

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Energy & Environmental Science Issue 5 out now

May’s issue of Energy & Environmental Science has now been published online – take a look today…

outside coverHere’s just some of the great content from this month’s issue:

Analysis article
Life-cycle analysis of product integrated polymer solar cells
Nieves Espinosa, Rafael García-Valverde and Frederik C. Krebs, Energy Environ. Sci., 2011, 4, 1547

Review
Carbon nanotubes and their composites in electrochemical applications
Grzegorz Lota, Krzysztof Fic and Elzbieta Frackowiak, Energy Environ. Sci., 2011, 4, 1592

inside coverPerspective
Nuclear fuel in generation II and III reactors: research issues related to high burn-up
C. Degueldre, J. Bertsch, G. Kuri and M. Martin, Energy Environ. Sci., 2011, 4, 1651

Issue 5 also features some great artwork:

The outside cover highlights the work by Vilas Pol and Michael Thackeray on lithium electrochemical cells (DOI: 10.1039/C0EE00256A) and the inside cover features electronic/ionic conducting membranes for artificial photosynthesis by Nate Lewis and colleagues (DOI: 10.1039/C0EE00384K).

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