What’s the best choice for supercapacitors: graphene or graphene oxide?

Graphene oxide may be a better choice as an electrode for supercapacitors than graphene because it exhibits higher capacitance, shorter processing time and is cheaper than graphene, say researchers from China.

Supercapacitors are promising energy storage devices for electric vehicles because of their high power densities and long cyclic lives.

Graphene, a two-dimensional nanosheet of graphite, has been the material of choice for supercapacitors because it possesses superior electrical conductivity, a high theoretical surface area and chemical tolerance. But, owing to the unavoidable aggregation of graphene nanosheets, the surface area is usually much lower than the theoretical one and its capacitance is generally in the range 100–200 F g-1.

Graphene oxide is an intermediate during the synthesis of graphene. Despite the fact that some graphene oxide-based nanocomposites have performed well in supercapacitors, it has been said that graphene oxide is not suitable as an electrode material because of its poor conductivity, but the team contradict this with their findings.

Read the article in full:
What Is the Choice for Supercapacitors: Graphene or Graphene Oxide?
B Xu, S Yue, Z Sui, X Zhang, S Hou, G Cao and Y Yang
Energy Environ. Sci., 2011, DOI: 10.1039/c1ee01198g

Digg This
Reddit This
Stumble Now!
Share on Facebook
Bookmark this on Delicious
Share on LinkedIn
Bookmark this on Technorati
Post on Twitter
Google Buzz (aka. Google Reader)

Energy & Environmental Science Most-Read Articles for Q1 2011

Top 25 most-read Energy & Environmental Science articles for Q1

Review of solutions to global warming, air pollution, and energy security
Mark Z. Jacobson
DOI: 10.1039/B809990C

Graphene based new energy materials
Yiqing Sun, Qiong Wu and Gaoquan Shi
DOI: 10.1039/C0EE00683A

Organic tandem solar cells: A review
Tayebeh Ameri, Gilles Dennler, Christoph Lungenschmied and Christoph J. Brabec
DOI: 10.1039/B817952B

Bulk nanostructured thermoelectric materials: current research and future prospects
A. J. Minnich, M. S. Dresselhaus, Z. F. Ren and G. Chen
DOI: 10.1039/B822664B

Flexible energy storage devices based on graphene paper
Hyeokjo Gwon, Hyun-Suk Kim, Kye Ung Lee, Dong-Hwa Seo, Yun Chang Park, Yun-Sung Lee, Byung Tae Ahn and Kisuk Kang
DOI: 10.1039/C0EE00640H

Carbon nanotubes for lithium ion batteries
Brian J. Landi, Matthew J. Ganter, Cory D. Cress, Roberta A. DiLeo and Ryne P. Raffaelle
DOI: 10.1039/B904116H

Development and challenges of LiFePO4 cathode material for lithium-ion batteries
Li-Xia Yuan, Zhao-Hui Wang, Wu-Xing Zhang, Xian-Luo Hu, Ji-Tao Chen, Yun-Hui Huang and John B. Goodenough
DOI: 10.1039/C0EE00029A

Graphene-based nanomaterials for energy storage
Martin Pumera
DOI: 10.1039/C0EE00295J

Highly active cobalt phosphate and borate based oxygen evolving catalysts operating in neutral and natural waters
Arthur J. Esswein, Yogesh Surendranath, Steven Y. Reece and Daniel G. Nocera
DOI: 10.1039/C0EE00518E

Nanostructured silicon for high capacity lithium battery anodes
Jeannine R. Szczech and Song Jin
DOI: 10.1039/C0EE00281J

Development of alternative photocatalysts to TiO2: Challenges and opportunities
María D. Hernández-Alonso, Fernando Fresno, Silvia Suárez and Juan M. Coronado
DOI: 10.1039/B907933E

CO2 capture by solid adsorbents and their applications: current status and new trends
Qiang Wang, Jizhong Luo, Ziyi Zhong and Armando Borgna
DOI: 10.1039/C0EE00064G

Vertically-aligned nanostructures of ZnO for excitonic solar cells: a review
Irene Gonzalez-Valls and Monica Lira-Cantu
DOI: 10.1039/B811536B

Carbon nanostructures for energy
Nazario Martin, Dirk M. Guldi, Andreas Hirsch
DOI: 10.1039/C1EE90001C

Catalytic routes for the conversion of biomass into liquid hydrocarbon transportation fuels
Juan Carlos Serrano-Ruiz and James A. Dumesic
DOI: 10.1039/C0EE00436G

Green energy storage materials: Nanostructured TiO2 and Sn-based anodes for lithium-ion batteries
Da Deng, Min Gyu Kim, Jim Yang Lee and Jaephil Cho
DOI: 10.1039/B823474D

The role of buffer layers in polymer solar cells
Riccardo Po, Chiara Carbonera, Andrea Bernardi and Nadia Camaioni
DOI: 10.1039/C0EE00273A

Electrospun nanofibers in energy and environmental applications
V. Thavasi, G. Singh and S. Ramakrishna
DOI: 10.1039/B809074M

Olivine LiFePO4: development and future
Yonggang Wang, Ping He and Haoshen Zhou
DOI: 10.1039/C0EE00176G

Nanostructured carbon-based electrodes: bridging the gap between thin-film lithium-ion batteries and electrochemical capacitors
Seung Woo Lee, Betar M. Gallant, Hye Ryung Byon, Paula T. Hammond and Yang Shao-Horn
DOI: 10.1039/C0EE00642D

Microalgae as biodiesel & biomass feedstocks: Review & analysis of the biochemistry, energetics & economics
Peter J. le B. Williams and Lieve M. L. Laurens
DOI: 10.1039/B924978H

High-performance Si microwire photovoltaics
Michael D. Kelzenberg, Daniel B. Turner-Evans, Morgan C. Putnam, Shannon W. Boettcher, Ryan M. Briggs, Jae Yeon Baek, Nathan S. Lewis and Harry A. Atwater
DOI: 10.1039/C0EE00549E

Bulk-heterojunction hybrid solar cells based on colloidal nanocrystals and conjugated polymers
Yunfei Zhou, Michael Eck and Michael Krüger
DOI: 10.1039/C0EE00143K

An overview of CO2 capture technologies
Niall MacDowell, Nick Florin, Antoine Buchard, Jason Hallett, Amparo Galindo, George Jackson, Claire S. Adjiman, Charlotte K. Williams, Nilay Shah and Paul Fennell
DOI: 10.1039/C004106H

Design of solid catalysts for the conversion of biomass
Roberto Rinaldi and Ferdi Schüth
DOI: 10.1039/B902668A

Digg This
Reddit This
Stumble Now!
Share on Facebook
Bookmark this on Delicious
Share on LinkedIn
Bookmark this on Technorati
Post on Twitter
Google Buzz (aka. Google Reader)

HOT Communication: Polymer/nanocrystal (NC) hybrid solar cells

Polymer/nanocrystal (NC) hybrid solar cells with an efficiency of 2.14% were fabricated from aqueous CdTe NCs and poly(p-phenylenevinylene) precursor.

Polymer NC solar cell

Read this ‘HOT’ Communication:
Efficient polymer/nanocrystal hybrid solar cells fabricated from aqueous materials
Weili Yu, Hao Zhang, Zhanxi Fan, Junhu Zhang, Haotong Wei, Ding Zhou, Bin Xu, Fenghong Li, Wenjing Tian and Bai Yang
Energy Environ. Sci., DOI: 10.1039/C1EE01485D

Digg This
Reddit This
Stumble Now!
Share on Facebook
Bookmark this on Delicious
Share on LinkedIn
Bookmark this on Technorati
Post on Twitter
Google Buzz (aka. Google Reader)

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

Digg This
Reddit This
Stumble Now!
Share on Facebook
Bookmark this on Delicious
Share on LinkedIn
Bookmark this on Technorati
Post on Twitter
Google Buzz (aka. Google Reader)

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

Digg This
Reddit This
Stumble Now!
Share on Facebook
Bookmark this on Delicious
Share on LinkedIn
Bookmark this on Technorati
Post on Twitter
Google Buzz (aka. Google Reader)

SuNEC 2011 conference

SuNECEnergy & Environmental Science is delighted to announce its exciting collaboration with the Sun New Energy Conference and Exhibition (SuNEC).

SuNEC will be held 5-7 July 2011 in Sicily, Italy and will be co-chaired by Vittorio Loddo and Mario Pagliaro. Confirmed plenary speakers include Ralph G. Nuzzo, Athanasios Konstandopoulos, Bernard Kippelen and Vincenzo Balzani.

The meeting will focus on the practical aspects of solar energy in every major field, covering the latest developments in solar energy science. For more information and to register for this conference, visit the SuNEC website.

Themes:

  • Photovoltaics
  • Solar electrical vehicles
  • BIPV
  • Solar cooling
  • Concentrated solar power
  • Solar thermal
  • Solar economy (Helionomics)

Energy & Environmental Science plans to publish a collection of high-profile feature articles in a special issue to highlight some of the great research from this important meeting in the area of solar energy conversion.

Energy & Environmental Science articles of interest:

Solar hydrogen: fuel of the near future
Mario Pagliaro, Athanasios G. Konstandopoulos, Rosaria Ciriminna and Giovanni Palmisano,
Energy Environ. Sci
., 2010, 3, 279

Compact monocrystalline silicon solar modules with high voltage outputs and mechanically flexible designs
Alfred J. Baca, Ki Jun Yu, Jianliang Xiao, Shuodao Wang, Jongseung Yoon, Jae Ha Ryu, Darren Stevenson, Ralph G. Nuzzo, Angus A. Rockett, Yonggang Huang and John A. Rogers,
Energy Environ. Sci.
, 2010, 3, 208

Digg This
Reddit This
Stumble Now!
Share on Facebook
Bookmark this on Delicious
Share on LinkedIn
Bookmark this on Technorati
Post on Twitter
Google Buzz (aka. Google Reader)

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

Digg This
Reddit This
Stumble Now!
Share on Facebook
Bookmark this on Delicious
Share on LinkedIn
Bookmark this on Technorati
Post on Twitter
Google Buzz (aka. Google Reader)

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.

Digg This
Reddit This
Stumble Now!
Share on Facebook
Bookmark this on Delicious
Share on LinkedIn
Bookmark this on Technorati
Post on Twitter
Google Buzz (aka. Google Reader)

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

Digg This
Reddit This
Stumble Now!
Share on Facebook
Bookmark this on Delicious
Share on LinkedIn
Bookmark this on Technorati
Post on Twitter
Google Buzz (aka. Google Reader)

Advisory Board Member Tom Moore featured in Science

Energy & Environmental Science Advisory Board member, Thomas Moore has a Review article in Science today:

Comparing Photosynthetic and Photovoltaic Efficiencies and Recognizing the Potential for Improvement
R. E. Blankenship et al.
DOI: 10.1126/science.1200165

You can also listen to a Podcast about the work!

See which other leading scientists are on the Energy & Environmental Science  Editorial and Advisory Boards

Submit your latest reseach to Energy & Environmental Science today – the leading journal in its ISI subject catagory!

Digg This
Reddit This
Stumble Now!
Share on Facebook
Bookmark this on Delicious
Share on LinkedIn
Bookmark this on Technorati
Post on Twitter
Google Buzz (aka. Google Reader)