If scientists are ever going to deliver on the promise of implantable artificial organs or clothing that dries itself, they'll first need to solve the problem of inflexible batteries that run out of juice too quickly. They're getting closer, and today researchers report that they've developed a new material by weaving two polymers together in a way that vastly increases charge storage capacity.
The researchers will present their work today at the 255th National Meeting & Exposition of the American Chemical Society (ACS).
"We had been developing polymer networks for a different application involving actuation and tactile sensing," Tiesheng Wang says. "After the project, we realized that the stretchable, bendable material we'd made could potentially be used for energy storage."
Batteries, specifically lithium-ion batteries, dominate the energy storage landscape. However, the chemical reactions underlying the charging and discharging process in batteries are slow, limiting how much power they can deliver. Plus, batteries tend to degrade over time, requiring replacement. An alternate energy storage device, the supercapacitor, charges rapidly and generates serious power, which could potentially allow electric cars to accelerate more quickly, among other applications. Plus, supercapacitors store energy electrostatically, not chemically, which makes them more stable and long-lasting than many batteries. But today's commercially available supercapacitors require binders and have low energy density, limiting their application in emerging go-anywhere electronics.
Wang, a graduate student in the lab of Stoyan Smoukov, Ph.D., at the University of Cambridge (U.K.) suspected that a flexible conducting polymer-based material from another project they were working on could be a better alternative. Conducting polymers, such as poly(3,4-ethylenedioxythiophene) (PEDOT), are candidate supercapacitors that have advantages over traditional carbon-based supercapacitors as charge storage materials. They are pseudocapacitive, meaning they allow reversible electrochemical reactions, and they also are chemically stable and inexpensive. However, ions can only penetrate the polymers a couple of nanometers deep, leaving much of the material as dead weight. Scientists working to improve ion mobility had previously developed nanostructures that deposit thin layers of conducting polymers on top of support materials, which improves supercapacitor performance by making more of the polymer accessible to the ions. The drawback, according to Wang, is that these nanostructures can be fragile, difficult to make reproducibly when scaled-up and poor in electrochemical stability, limiting their applicability.
So, Smoukov and Wang developed a more robust material by weaving together a conducting polymer with an ion-storage polymer. The two polymers were stitched together to form a candy cane-like geometry, with one polymer playing the role of the white stripe and the other, red. While PEDOT conducts electricity, the other polymer, poly(ethylene oxide) (PEO), can store ions. The interwoven geometry is instrumental to the energy storage benefits, Wang says, because it allows the ions to access more of the material overall, approaching the "theoretical limit."
When tested, the candy cane supercapacitor demonstrated improvements over PEDOT alone with regard to flexibility and cycling stability. It also had nearly double the specific capacitance compared to conventional PEDOT-based supercapacitors.
Still, there's room for improvement, Smoukov says. "In future experiments, we will be substituting polyaniline for PEDOT to increase the capacitance," he says. "Polyaniline, because it can store more charge per unit of mass, could potentially store three times as much electricity as PEDOT for a given weight." That means lighter batteries with the same energy storage can be charged faster, which is an important consideration in the development of novel wearables, robots and other devices.
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More information: Title: Candy cane-like semi-interpenetrating polymer networks for enhanced fast-charging power source of electronics
Pseudocapacitance is a material property that allows ions to enter inside the material and thus pack much more charge than carbon ones that mostly store the charge near the surface (in the so-called double layer). Conducting polymers show great promise as supercapacitor materials due to their high pseudocapacitance, low cost, toughness, and flexibility. The problem with polymer-based supercapacitors, however, is that the ions necessary for these chemical reactions can only access the top few nanometers below the material surface, leaving the rest of the electrode as dead weight. Here, we use semi-interpenetrating networks (sIPNs) of a pseudocapacitive polymer in an ionically conductive polymer matrix to decrease ion diffusion length scales and make virtually all of the active material accessible for charge storage. Our freestanding poly(3,4-ethylenedioxythiophene)/poly(ethylene oxide) (PEDOT/PEO) sIPN films yield simultaneous improvements in three crucial elements of supercapacitor performance: specific capacitance (182 F/g, approaching the theoretical limit of PEDOT), cycling stability (97.5% capacitance retention after 3000 cycles), and flexibility (the electrodes bend to a <200 μm radius of curvature without breaking). The supercapacitor based on our material, which is known as "Candy Cane Supercapacitor", could power electronics embedded in smart clothing, wearable and implantable devices, and soft robotics.