Showing posts with label battery. Show all posts
Showing posts with label battery. Show all posts

Wednesday, February 18, 2015

New Paper-like Material Could Boost Electric Vehicle Batteries

Microscopic images of silicon nanofibers
Scanning electron microscope images of
(a) SiO2 nanofibers after drying, (b) SiO2
nanofibers under high magnification (c) silicon
nanofibers after etching, and (d) silicon nanofibers
under high magnification.
Researchers at the University of California, Riverside’s Bourns College of Engineering have developed a novel paper-like material for lithium-ion batteries. It has the potential to boost by several times the specific energy, or amount of energy that can be delivered per unit weight of the battery.
This paper-like material is composed of sponge-like silicon nanofibers more than 100 times thinner than human hair. It could be used in batteries for electric vehicles and personal electronics.
The findings were just published in a paper, “Towards Scalable Binderless Electrodes: Carbon Coated Silicon Nanofiber Paper via Mg Reduction of Electrospun SiO2 Nanofibers,” in the journal Nature Scientific Reports. The authors were Mihri Ozkan, a professor of electrical and computer engineering, Cengiz S. Ozkan, a professor of mechanical engineering, and six of their graduate students: Zach Favors, Hamed Hosseini Bay, Zafer Mutlu, Kazi Ahmed, Robert Ionescu and Rachel Ye.
The nanofibers were produced using a technique known as electrospinning, whereby 20,000 to 40,000 volts are applied between a rotating drum and a nozzle, which emits a solution composed mainly of tetraethyl orthosilicate (TEOS), a chemical compound frequently used in the semiconductor industry. The nanofibers are then exposed to magnesium vapor to produce the sponge-like silicon fiber structure.
Conventionally produced lithium-ion battery anodes are made using copper foil coated with a mixture of graphite, a conductive additive, and a polymer binder. But, because the performance of graphite has been nearly tapped out, researchers are experimenting with other materials, such as silicon, which has a specific capacity, or electrical charge per unit weight of the battery, nearly 10 times higher than graphite.
silicon nanofiber images
(a) Schematic representation of the electrospinning
process and subsequent reduction process. Digital
photographs of (b) as-spun SiO2 nanofibers paper, (c)
etched silicon nanofiber paper, and (d) carbon-coated silicon
nanofiber paper as used in the lithium-ion half-cell
configuration.
The problem with silicon is that is suffers from significant volume expansion, which can quickly degrade the battery. The silicon nanofiber structure created in the Ozkan’s labs circumvents this issue and allows the battery to be cycled hundreds of times without significant degradation.
“Eliminating the need for metal current collectors and inactive polymer binders while switching to an energy dense material such as silicon will significantly boost the range capabilities of electric vehicles,” Favors said.
This technology also solves a problem that has plagued free-standing, or binderless, electrodes for years: scalability. Free-standing materials grown using chemical vapor deposition, such as carbon nanotubes or silicon nanowires, can only be produced in very small quantities (micrograms). However, Favors was able to produce several grams of silicon nanofibers at a time even at the lab scale.
The researchers’ future work involves implementing the silicon nanofibers into a pouch cell format lithium-ion battery, which is a larger scale battery format that can be used in EVs and portable electronics.
The research is supported by Temiz Energy Technologies. The UC Riverside Office of Technology Commercialization has filed patents for inventions reported in the research paper.
http://ucrtoday.ucr.edu/27263

Thursday, February 20, 2014

ORNL microscopy system delivers real-time view of battery electrochemistry

A new in situ transmission electron microscopy technique
enabled  ORNL researchers to image the snowflake-like
growth of the  solid electrolyte interphase from a working
battery electrode. 
Using a new microscopy method, researchers at the Department of Energy’s Oak Ridge National Laboratory can image and measure electrochemical processes in batteries in real time and at nanoscale resolution.
Scientists at ORNL used a miniature electrochemical liquid cell that is placed in a transmission electron microscope to study an enigmatic phenomenon in lithium-ion batteries called the solid electrolyte interphase, or SEI, as described in a study published in Chemical Communications.
The SEI is a nanometer-scale film that forms on a battery’s negative electrode due to electrolyte decomposition. Scientists agree that the SEI’s formation and stability play key roles in controlling battery functionality. But after three decades of research in the battery field, details of the SEI’s dynamics, structure and chemistry during electrochemical cycling are still debated, stemming from inherent difficulties in studying battery electrode materials in their native liquid environment.
 “We’ve used this novel in situ method to understand the dynamics of how this layer forms and evolves during battery operation,” said Raymond Unocic, ORNL R&D staff scientist.
Battery researchers typically study the structure and chemistry of the SEI through “post-mortem” methods, in which a cycled battery is disassembled, dried and then analyzed through a number of characterization methods.
“This is problematic because of the air and moisture sensitivity of the SEI, and the ease by which environmental exposure can modify its structure and chemistry.” Unocic said.
The ORNL researchers formed a miniature electrochemical cell by enclosing battery electrolyte between two silicon microchip devices that contain microfabricated electrodes and silicon nitride viewing membranes. The transparent “windows” seal the highly volatile battery electrolyte from the microscope’s vacuum environment and allow the electron beam to pass through the liquid, which facilitates imaging of the electrochemical reaction products as they form.  
To reproduce a battery charging cycle, the researchers applied a potential at the working electrode and monitored the resulting changes in current. The most striking result, said the researchers, was capturing an unprecedented view of SEI evolution during potential cycling. The technique is able to image the formation of tiny crystalline particles only one billionth of a meter in size.
“As we start to sweep the potential, we didn’t initially observe anything,” said lead author Robert Sacci, a postdoctoral research fellow with ORNL’s FIRST Energy Frontier Research Center. “Then we started seeing shadows -- presumably polymeric SEI -- forming into a dendritic pattern. It looks like a snowflake forming from the electrode.” Watch a video of the process at http://www.youtube.com/watch?v=OHrlFNB-Q9Y.
The researchers plan to build on this initial proof-of-principle study to better understand the factors behind the SEI’s formation, which could ultimately help improve battery performance, capacity, and safety at the device level.
“Tailoring the SEI’s structure and chemistry to maximize battery capabilities appears to be a delicate balancing act,” Unocic said. “When you cycle a real battery, the interphase structure can form, break, and reform again, depending on how thick the layer grows, so we need to look at improving its structural stability. But at the same time, we have to think about making the interphase more efficient for lithium ion transport. This study brings us one step closer to understanding SEI formation and growth.”
Next steps for the researchers include applying their technique to study different types of battery electrodes and electrolytes and other energy storage systems including fuel cells and supercapacitors.
Coauthors are ORNL’s Raymond Unocic, Robert Sacci, Nancy Dudney and Karren More; and Pacific Northwest National Laboratory’s Lucas Parent, Ilke Arslan, Nigel Browning. The study is published as “Direct Visualization of Initial SEI Morphology and Growth Kinetics During Lithium Deposition by in situ Electrochemical Transmission Electron Microscopy.”
The research was supported by the DOE’s Office of Energy Efficiency and Renewable Energy, Vehicle Technologies Program, by the Fluid Interface Reactions Structures and Transport (FIRST) Center, an Energy Frontier Research Center funded by the Office of Basic Energy Sciences, and as part of a user proposal at ORNL’s Center for Nanophase Materials Sciences. Parts of the work were supported by the laboratory directed research and development program at Pacific Northwest National Laboratory and the Joint Center for Energy Storage Research, an Energy Innovation Hub funded by BES-DOE.
Part of this research was conducted at the Center for Nanophase Materials Sciences, which is sponsored at ORNL by the Scientific User Facilities Division in DOE’s Office of Basic Energy Sciences. CNMS is one of the five DOE Nanoscale Science Research Centers supported by the DOE Office of Science, premier national user facilities for interdisciplinary research at the nanoscale. Together the NSRCs comprise a suite of complementary facilities that provide researchers with state-of-the-art capabilities to fabricate, process, characterize and model nanoscale materials, and constitute the largest infrastructure investment of the National Nanotechnology Initiative. The NSRCs are located at DOE's Argonne, Brookhaven, Lawrence Berkeley, Oak Ridge and Sandia and Los Alamos national laboratories. For more information about the DOE NSRCs, please visit http://science.energy.gov/bes/suf/user-facilities/nanoscale-science-research-centers/.
UT-Battelle manages ORNL for the Department of Energy’s Office of Science. DOE’s Office of Science is the single largest supporter of basic research in the physical sciences in the United States, and is working to address some of the most pressing challenges of the time. For more information, please visit science.energy.gov.
Source: http://www.ornl.gov/ornl/news/news-releases/2014/ornl-microscopy-system-delivers-real-time-view-of-battery-electrochemistry

Monday, January 13, 2014

Technology uses micro-windmills to recharge cell phones

A single grain of rice could hold about 10 of these tiny windmills.

A UT Arlington research associate and electrical engineering professor have designed a micro-windmill that generates wind energy and may become an innovative solution to cell phone batteries constantly in need of recharging and home energy generation where large windmills are not preferred.

Smitha Rao and J.-C. Chiao designed and built the device that is about 1.8 mm at its widest point. A single grain of rice could hold about 10 of these tiny windmills. Hundreds of the windmills could be embedded in a sleeve for a cell phone. Wind, created by waving the cell phone in air or holding it up to an open window on a windy day, would generate the electricity that could be collected by the cell phone’s battery.


Rao’s works in micro-robotic devices initially heightened a Taiwanese company’s interest in having Rao and Chiao brainstorm over novel device designs and applications for the company’s unique fabrication techniques, which are known in the semiconductor industry for their reliability.


UT Arlington Research Associate Smitha Rao


“The company was quite surprised with the micro-windmill idea when we showed the demo video of working devices,” Rao said. “It was something completely out of the blue for them and their investors.”

Rao’s designs blend origami concepts into conventional wafer-scale semiconductor device layouts so complex 3-D moveable mechanical structures can be self-assembled from two-dimensional metal pieces utilizing planar multilayer electroplating techniques that have been optimized by WinMEMS Technologies Co., the Taiwanese fabrication foundry that took an initial interest in Rao’s work.

“The micro-windmills work well because the metal alloy is flexible and Smitha’s design follows minimalism for functionality.” Chiao said.

WinMEMS became interested in the micro-electro mechanical system research and started a relationship with UT Arlington. Company representatives visited with the UT Arlington team several times in 2013 to discuss collaboration.

An agreement has been established for UT Arlington to hold the intellectual properties while WinMEMS explores the commercialization opportunities. UT Arlington has applied for a provisional patent.

Currently, WinMEMS has been showcasing UT Arlington’s works on its website and in public presentations, which include the micro-windmills, gears, inductors, pop-up switches and grippers. All of those parts are as tiny as a fraction of the diameter of a human hair.

These inventions are essential to build micro-robots that can be used as surgical tools, sensing machines to explore disaster zones or manufacturing tools to assemble micro-machines.

“It’s very gratifying to first be noticed by an international company and second to work on something like this where you can see immediately how it might be used,” said Rao, who earned her Ph.D in 2009 at UT Arlington. “However, I think we’ve only scratched the surface on how these micro-windmills might be used.”

The micro windmills were tested successfully in September 2013 in Chiao’s lab. The windmills operate under strong artificial winds without any fracture in the material because of the durable nickel alloy and smart aerodynamic design.

“The problem most MEMS designers have is that materials are too brittle,” Rao said. “With the nickel alloy, we don’t have that same issue. They’re very, very durable.”

The micro-windmills can be made in an array using the batch processes. The fabrication cost of making one device is the same as making hundreds or thousands on a single wafer, which enables for mass production of very inexpensive systems.

“Imagine that they can be cheaply made on the surfaces of portable electronics,” Chiao said, “so you can place them on a sleeve for your smart phone. When the phone is out of battery power, all you need to do is to put on the sleeve, wave the phone in the air for a few minutes and you can use the phone again.”

Chiao said because of the small sizes, flat panels with thousand of windmills could be made and mounted on the walls of houses or building to harvest energy for lighting, security or environmental sensing and wireless communication.

He added that it has been fulfilling to see his former student succeed and help move innovation toward the marketplace.

“To see a company recognize that and seek you out for your expertise speaks volumes about what UT Arlington means to the world,” he said proudly.

Source: http://www.uta.edu/news/releases/2014/01/microwindmill-rao-chiao.php#!

Wednesday, January 8, 2014

Battery offers renewable energy breakthrough

“Imagine a device the size of a home heating-oil tank sitting in your basement. It would store a day’s worth of sunshine from the solar panels on the roof of your house …” — Michael Marshak

Harvard technology could economically store energy for use when the wind doesn’t blow and the sun doesn’t shine

A team of Harvard scientists and engineers has demonstrated a new type of battery that could fundamentally transform the way electricity is stored on the grid, making power from renewable energy sources such as wind and sun far more economical and reliable.

The novel battery technology is reported in a paper published in Nature on Jan. 9. Under the OPEN 2012 program, the Harvard team received funding from the U.S. Department of Energy’s Advanced Research Projects Agency — Energy (ARPA-E) to develop the grid-scale battery, and plans to work with the agency to catalyze further technological and market breakthroughs over the next several years.

The paper describes a metal-free flow battery that relies on the electrochemistry of naturally abundant, inexpensive, small organic (carbon-based) molecules called quinones, which are similar to molecules that store energy in plants and animals.

The mismatch between the availability of intermittent wind or sunshine and the variable demand is the biggest obstacle to using renewable sources for a large fraction of our electricity. A cost-effective means of storing large amounts of electrical energy could solve this problem.

The battery was designed, built, and tested in the laboratory of Michael J. Aziz, the Gene and Tracy Sykes Professor of Materials and Energy Technologies at the Harvard School of Engineering and Applied Sciences (SEAS). Roy G. Gordon, the Thomas Dudley Cabot Professor of Chemistry and Professor of Materials Science, led the work on the synthesis and chemical screening of molecules. Alán Aspuru-Guzik, professor of chemistry and chemical biology, used his pioneering high-throughput molecular screening methods to calculate the properties of more than 10,000 quinone molecules in search of the best candidates for the battery.

Flow batteries store energy in chemical fluids contained in external tanks, as with fuel cells, instead of within the battery container itself. The two main components — the electrochemical conversion hardware through which the fluids are flowed (which sets the peak power capacity) and the chemical storage tanks (which set the energy capacity) — may be independently sized. Thus the amount of energy that can be stored is limited only by the size of the tanks. The design permits larger amounts of energy to be stored at lower cost than with traditional batteries.

By contrast, in solid-electrode batteries, such as those commonly found in cars and mobile devices, the power conversion hardware and energy capacity are packaged together in one unit and cannot be decoupled. Consequently they maintain peak discharge power for less than an hour before they are drained, and are therefore ill-suited to store intermittent renewables.

“Our studies indicate that one to two days’ worth of storage is required for making solar and wind dispatchable through the electrical grid,” said Aziz.

To store 50 hours of energy from a 1-megawatt power capacity wind turbine (50 megawatt-hours), for example, a possible solution would be to buy traditional batteries with 50 megawatt-hours of energy storage, but they would come with 50 megawatts of power capacity. Paying for 50 megawatts of power capacity when only 1 megawatt is necessary makes little economic sense.

For this reason, a growing number of engineers have focused their attention on flow-battery technology. But until now, flow batteries have relied on chemicals that are expensive or hard to maintain, driving up the cost of storing energy.

The active components of electrolytes in most flow batteries have been metals. Vanadium is used in the most commercially advanced flow-battery technology now in development, but it sets a rather high floor on the cost per kilowatt-hour at any scale. Other flow batteries contain precious metal electrocatalysts, such as the platinum used in fuel cells.

The new flow battery developed by the Harvard team already performs as well as vanadium flow batteries, with chemicals that are significantly less expensive, and with no precious-metal electrocatalyst.

“The whole world of electricity storage has been using metal ions in various charge states, but there is a limited number that you can put into solution and use to store energy, and none of them can economically store massive amounts of renewable energy,” Gordon said. “With organic molecules, we introduce a vast new set of possibilities. Some of them will be terrible and some will be really good. With these quinones we have the first ones that look really good.”

Aspuru-Guzik noted that the project is very well aligned with the White House Materials Genome Initiative. “This project illustrates what the synergy of high-throughput quantum chemistry and experimental insight can do,” he said. “In a very quick time period, our team homed in to the right molecule. Computational screening, together with experimentation, can lead to discovery of new materials in many application domains.”

Quinones are abundant in crude oil as well as in green plants. The molecule the Harvard team used in its first quinone-based flow battery is almost identical to one found in rhubarb. The quinones are dissolved in water, which prevents them from catching fire.

To back up a commercial wind turbine, a large storage tank would be needed, possibly located in a below-grade basement, said co-lead author Michael Marshak, a postdoctoral fellow at SEAS and in the Department of Chemistry and Chemical Biology. With a whole field of turbines or a large solar farm, one could imagine a few very large storage tanks.

The same technology could also have applications at the consumer level, Marshak said. “Imagine a device the size of a home heating-oil tank sitting in your basement. It would store a day’s worth of sunshine from the solar panels on the roof of your house, potentially providing enough to power your household from late afternoon, through the night, into the next morning, without burning any fossil fuels.”

“The Harvard team’s results published in Nature demonstrate an early, yet important technical achievement that could be critical in furthering the development of grid-scale batteries,” said ARPA-E Program Director John Lemmon. “The project team’s result is an excellent example of how a small amount of catalytic funding from ARPA-E can help build the foundation to hopefully turn scientific discoveries into low-cost, early-stage energy technologies.”

Team leader Aziz said the next steps in the project will be to further test and optimize the system that has been demonstrated on the benchtop and bring it toward a commercial scale. “So far, we’ve seen no sign of degradation after more than 100 cycles, but commercial applications require thousands of cycles,” he said. He also expects to achieve significant improvements in the underlying chemistry of the battery system. “I think the chemistry we have right now might be the best that’s out there for stationary storage and quite possibly cheap enough to make it in the marketplace,” he said. “But we have ideas that could lead to huge improvements.”

By the end of the three-year development period, Connecticut-based Sustainable Innovations, LLC, a collaborator on the project, expects to deploy demonstration versions of the organic flow battery contained in a unit the size of a horse trailer. The portable, scaled-up storage system could be hooked up to solar panels on the roof of a commercial building, and electricity from the solar panels could either directly supply the needs of the building or go into storage and come out of storage when needed. Sustainable Innovations anticipates playing a key role in the product’s commercialization by leveraging its ultra-low-cost electrochemical cell design and system architecture already under development for energy storage applications.

“You could theoretically put this on any node on the grid,” Aziz said. “If the market price fluctuates enough, you could put a storage device there and buy electricity to store it when the price is low and then sell it back when the price is high. In addition, you might be able to avoid the permitting and gas-supply problems of having to build a gas-fired power plant just to meet the occasional needs of a growing peak demand.”

This technology could also provide very useful backup for off-grid rooftop solar panels — an important advantage considering some 20 percent of the world’s population does not have access to a power distribution network.

“The intermittent renewables storage problem is the biggest barrier to getting most of our power from the sun and the wind,” Aziz said. “A safe and economical flow battery could play a huge role in our transition off fossil fuels to renewable electricity. I’m excited that we have a good shot at it.”

William Hogan, Raymond Plank Professor of Global Energy Policy at Harvard Kennedy School and one of the world’s foremost experts on electricity markets, is helping the team explore the economic drivers for the technology.

Trent M. Molter, president and CEO of Sustainable Innovations, LLC, provides expertise on implementing the Harvard team’s technology into commercial electrochemical systems.

Monday, November 18, 2013

Scientists Invent Self-healing Battery Electrode

An electron micrograph shows cracks left in a self-healing polymer
coating due to swelling of its silicon electrode during charging. Right:
Five hours later, the smaller cracks have healed.
(C. Wang et al, Nature Chemistry)
Researchers have made the first battery electrode that heals itself, opening a new and potentially commercially viable path for making the next generation of lithium ion batteries for electric cars, cell phones and other devices. 
The secret is a stretchy polymer that coats the electrode, binds it together and spontaneously heals tiny cracks that develop during battery operation, said the team from Stanford University and the Department of Energy’s (DOE) SLAC National Accelerator Laboratory.
They report the advance in the Nov. 19 issue of Nature Chemistry.
“Self-healing is very important for the survival and long lifetimes of animals and plants,” said Chao Wang, a postdoctoral researcher at Stanford and one of two principal authors of the paper. “We want to incorporate this feature into lithium ion batteries so they will have a long lifetime as well.”
Chao developed the self-healing polymer in the lab of Stanford Professor Zhenan Bao, whose group has been working on flexible electronic skin for use in robots, sensors, prosthetic limbs and other applications. For the battery project he added tiny nanoparticles of carbon to the polymer so it would conduct electricity.
”We found that silicon electrodes lasted 10 times longer when coated with the self-healing polymer, which repaired any cracks within just a few hours,” Bao said.

“Their capacity for storing energy is in the practical range now, but we would certainly like to push that,” said Yi Cui, an associate professor at SLAC and Stanford who led the research with Bao. The electrodes worked for about 100 charge-discharge cycles without significantly losing their energy storage capacity. “That’s still quite a way from the goal of about 500 cycles for cell phones and 3,000 cycles for an electric vehicle,” Cui said, “but the promise is there, and from all our data it looks like it’s working.”
Researchers worldwide are racing to find ways to store more energy in the negative electrodes of lithium ion batteries to achieve higher performance while reducing weight. One of the most promising electrode materials is silicon; it has a high capacity for soaking up lithium ions from the battery fluid during charging and then releasing them when the battery is put to work.
But this high capacity comes at a price: Silicon electrodes swell to three times normal size and shrink back down again each time the battery charges and discharges, and the brittle material soon cracks and falls apart, degrading battery performance. This is a problem for all electrodes in high-capacity batteries, said Hui Wu, a former Stanford postdoc who is now a faculty member at Tsinghua University in Beijing, the other principal author of the paper.
To make the self-healing coating, scientists deliberately weakened some of the chemical bonds within polymers – long, chain-like molecules with many identical units. The resulting material breaks easily, but the broken ends are chemically drawn to each other and quickly link up again, mimicking the process that allows biological molecules such as DNA to assemble, rearrange and break down.
To show how flexible their self-healing polymer is, researchers coated a balloon with it and then inflated and deflated the balloon repeatedly, mimicking the swelling and shrinking of a silicon electrode during battery operation. The polymer stretches but does not crack. (Brad Plummer/SLAC)
Researchers in Cui’s lab and elsewhere have tested a number of ways to keep silicon electrodes intact and improve their performance. Some are being explored for commercial uses, but many involve exotic materials and fabrication techniques that are challenging to scale up for production.
The self-healing electrode, which is made from silicon microparticles that are widely used in the semiconductor and solar cell industries, is the first solution that seems to offer a practical road forward, Cui said. The researchers said they think this approach could work for other electrode materials as well, and they will continue to refine the technique to improve the silicon electrode’s performance and longevity.
The research team also included Zheng Chen and Matthew T. McDowell of Stanford. Cui and Bao are members of the Stanford Institute for Materials and Energy Sciences, a joint SLAC/Stanford institute. The research was funded by DOE through SLAC’s Laboratory Directed Research and Development program and by the Precourt Institute for Energy at Stanford University.
SLAC is a multi-program laboratory exploring frontier questions in photon science, astrophysics, particle physics and accelerator research. Located in Menlo Park, California, SLAC is operated by Stanford University for the U.S. Department of Energy Office of Science. To learn more, please visitwww.slac.stanford.edu.
The Stanford Institute for Materials and Energy Sciences (SIMES) is a joint institute of SLAC National Accelerator Laboratory and Stanford University. SIMES studies the nature, properties and synthesis of complex and novel materials in the effort to create clean, renewable energy technologies. For more information, please visit simes.slac.stanford.edu.

Wednesday, November 13, 2013

Better batteries through biology?

MIT researchers find a way to boost lithium-air battery performance, with the help of modified viruses.

Lithium-air batteries have become a hot research area in recent years: They hold the promise of drastically increasing power per battery weight, which could lead, for example, to electric cars with a much greater driving range. But bringing that promise to reality has faced a number of challenges, including the need to develop better, more durable materials for the batteries’ electrodes and improving the number of charging-discharging cycles the batteries can withstand.

Now, MIT researchers have found that adding genetically modified viruses to the production of nanowires — wires that are about the width of a red blood cell, and which can serve as one of a battery’s electrodes — could help solve some of these problems.

The new work is described in a paper published in the journal Nature Communications, co-authored by graduate student Dahyun Oh, professors Angela Belcher and Yang Shao-Horn, and three others. The key to their work was to increase the surface area of the wire, thus increasing the area where electrochemical activity takes place during charging or discharging of the battery.

The researchers produced an array of nanowires, each about 80 nanometers across, using a genetically modified virus called M13, which can capture molecules of metals from water and bind them into structural shapes. In this case, wires of manganese oxide — a “favorite material” for a lithium-air battery’s cathode, Belcher says — were actually made by the viruses. But unlike wires “grown” through conventional chemical methods, these virus-built nanowires have a rough, spiky surface, which dramatically increases their surface area.

Belcher, the W.M. Keck Professor of Energy and an affiliate of MIT’s Koch Institute for Integrative Cancer Research, explains that this process of biosynthesis is “really similar to how an abalone grows its shell” — in that case, by collecting calcium from seawater and depositing it into a solid, linked structure. 


The increase in surface area produced by this method can provide “a big advantage,” Belcher says, in lithium-air batteries’ rate of charging and discharging. But the process also has other potential advantages, she says: Unlike conventional fabrication methods, which involve energy-intensive high temperatures and hazardous chemicals, this process can be carried out at room temperature using a water-based process.

Also, rather than isolated wires, the viruses naturally produce a three-dimensional structure of cross-linked wires, which provides greater stability for an electrode.

A final part of the process is the addition of a small amount of a metal, such as palladium, which greatly increases the electrical conductivity of the nanowires and allows them to catalyze reactions that take place during charging and discharging. Other groups have tried to produce such batteries using pure or highly concentrated metals as the electrodes, but this new process drastically lowers how much of the expensive material is needed.

Altogether, these modifications have the potential to produce a battery that could provide two to three times greater energy density — the amount of energy that can be stored for a given weight — than today’s best lithium-ion batteries, a closely related technology that is today's top contender, the researchers say.

Belcher emphasizes that this is early-stage research, and much more work is needed to produce a lithium-air battery that’s viable for commercial production. This work only looked at the production of one component, the cathode; other essential parts, including the electrolyte — the ion conductor that lithium ions traverse from one of the battery’s electrodes to the other — require further research to find reliable, durable materials. Also, while this material was successfully tested through 50 cycles of charging and discharging, for practical use a battery must be capable of withstanding thousands of these cycles.

While these experiments used viruses for the molecular assembly, Belcher says that once the best materials for such batteries are found and tested, actual manufacturing might be done in a different way. This has happened with past materials developed in her lab, she says: The chemistry was initially developed using biological methods, but then alternative means that were more easily scalable for industrial-scale production were substituted in the actual manufacturing.

Jie Xiao, a research scientist at the Pacific Northwest National Laboratory who was not involved in this work, calls it “a great contribution to guide the research on how to effectively manipulate” catalysis in lithium-air batteries. He says this “novel approach … not only provides new insights for lithium-air batteries,” but also “the template introduced in this work is also readily adaptable for other catalytic systems.”

In addition to Oh, Belcher, and Shao-Horn, the work was carried out by MIT research scientists Jifa Qi and Yong Zhang and postdoc Yi-Chun Lu. The work was supported by the U.S. Army Research Office and the National Science Foundation.


Source: http://web.mit.edu/newsoffice/2013/better-batteries-through-biology-1113.html