http://news.sciencemag.org/chemistry/2015/08/new-electric-storage-material-could-put-more-zip-your-tesla
New electric storage material could put more zip in your Tesla
By Robert F. Service  21 August 2015

[image  / Aperture Focal/iStockphoto
http://news.sciencemag.org/sites/default/files/styles/thumb_article_l/public/sn-electricstorage.jpg
Researchers have developed a new electric storage material that’s among the
best now available—an advance that could allow automakers to build faster
charging electric cars
]

BOSTON—The next electric car you buy might have a little extra zip. That’s
because researchers have developed a new electric storage material that’s
among the best at holding large amounts of charge as well as charging and
discharging in just seconds, they report this week. Moreover, because the
starting materials for making it are commercially available and relatively
cheap, it may prove more useful than higher performance—yet more
exotic—materials currently under development. That could eventually allow
automakers to build faster charging electric cars with a longer driving
range than any on the road today.

The new material, called a covalent organic framework (COF), is a highly
porous crystal. It’s used to store electricity in the heart of devices
called supercapacitors, which are widely used in everything from cars to
computers. In their simplest form, supercapacitors consist simply of two
metal electrodes separated by a conducting liquid, or electrolyte. To charge
the device, you apply a voltage between the two electrodes. That causes
oppositely charged ions to snuggle up to the surface of the electrodes,
where they remain even after the voltage is turned off. When the
supercapacitor is discharging, electrons flow from the negatively charged
electrode to the positive one, doing work along the way.

Because the transfer of electric charges happens so fast, supercapacitors
can be charged and discharged in seconds, compared with the hours it takes
for batteries. That’s made them ideal for applications such as regenerative
braking systems in electric cars, which use the energy in braking to
generate an electric current that is stored instantly.

The trouble is that the storage capacity of supercapacitors is limited by
the surface area of the electrodes, which is far less than the volume-based
storage of a battery. Not surprisingly, companies have sought to increase
the surface area of their electrodes by making them out of porous,
conductive materials like activated carbons, which now dominate the market.
Of course, they are always looking to do better.

One solution is materials with very high surface areas, such as carbon
nanotubes and graphene. Both of these are made from single layers of carbon
atoms, and have been used to make the highest capacity supercapacitors to
date. But the materials themselves remain expensive and relatively difficult
to produce in the volumes that would be needed for large-scale applications.
Another electrode-building material is redox-active molecules, which readily
absorb electrons and later give them back up. But redox-active materials
have their own challenges. Some fall apart after electrons cycle on and off
a few times, and others aren’t porous enough for making good
supercapacitors.

William Dichtel, a chemist at Cornell University, showed 2 years ago that
COFs can do better. Dichtel and colleagues reported making the first-ever
redox-active COF, assembled from organic building blocks
2,6-diaminoanthraquinone (DAAQ) and 1,3,5-triformylphluroglucinol (TFP).
Under the right conditions, Dichtel’s team found that DAAQ and TFP
spontaneously assemble themselves into large hexagonal rings with single
holes in the center. What’s more, the hexagons link together like sheets of
tiles on a bathroom floor. Additional sheets form on top of the first with
all the holes lining up. Ultimately, the material becomes a regular crystal
of tiled and stacked hexagons shot through with tiny pores, giving them a
surface area similar to activated carbons.

But because redox-active COFs have the ability to absorb electrons as well,
they have the potential to make better supercapacitor electrodes. Earlier
this year, the researchers reported that when they grew their material as
thin sheets atop a gold electrode, the COF had a capacity of about 160
farads per gram (F/g) of material. That wasn’t yet as good as the best
commercial supercapacitors. The problem was the COFs themselves weren’t very
conductive, even though they could charge and discharge quickly and hold an
impressive 12 electrons per hexagonal tile. The lack of conductivity meant
that the electrons in the upper portion of any COF more than 200 nanometers
thick wouldn’t be able to make it to the electrode. “There was no way to get
the charges out of the thicker films,” Dichtel says.

Until now. At the meeting of the American Chemical Society here this week,
Dichtel reported that he and his team got over their size hurdle by coating
their thick DAAQ-TFT COFs with a thin layer of the conducting polymer poly
3,4-ethylenedioxythiophene, known as PEDOT. The result was that all the
stored charges could zip through the PEDOT into the underlying gold
electrode, giving them a capacitance of 350 F/g, higher than any
supercapacitor on the market today. That’s still well below the 3300 F/g
numbers reported for a carbon nanotube–based device. But because the organic
building blocks are readily available, new COF-based supercapacitors could
have an easier path to market.

“It’s neat stuff,” says George Whitesides, a chemist at Harvard University.
Whitesides cautions that it’s still early days for COF-based
supercapacitors, as they must be proven robust enough to handle automotive
applications, among others. But Dichtel notes that his materials have
already withstood thousands of charge-discharge cycles without showing any
signs of degradation. As well, Dichtel says, there are lots of other redox
active molecules that can be used to make COFs, so there’s hope for doing
even better. “We are just at the very beginning of this,” he says. Already,
they’re doing pretty well.
[© sciencemag.org]




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