Browsing by Author "Lutkenhaus, Jodie L."

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    Highly Flexible Self-Assembled V2O5 Cathodes Enabled by Conducting Diblock Copolymers
    (Macmillan Publishers Limited, 2015) An, Hyosung; Mike, Jared; Smith, Kendall A.; Swank, Lisa; Lin, Yen-Hao; Pesek, Stacy L.; Verduzco, Rafael; Lutkenhaus, Jodie L.
    Mechanically robust battery electrodes are desired for applications in wearable devices, flexible displays, and structural energy and power. In this regard, the challenge is to balance mechanical and electrochemical properties in materials that are inherently brittle. Here, we demonstrate a unique water-based self-assembly approach that incorporates a diblock copolymer bearing electron- and ion-conducting blocks, poly(3-hexylthiophene)-block-poly(ethyleneoxide) (P3HT-b-PEO), with V2O5 to form a flexible, tough, carbon-free hybrid battery cathode. V2O5 is a promising lithium intercalation material, but it remains limited by its poor conductivity and mechanical properties. Our approach leads to a unique electrode structure consisting of interlocking V2O5 layers glued together with micellar aggregates of P3HT-b-PEO, which results in robust mechanical properties, far exceeding the those obtained from conventional fluoropolymer binders. Only 5 wt % polymer is required to triple the flexibility of V2O5, and electrodes comprised of 10 wt % polymer have unusually high toughness (293 kJ/m(3)) and specific energy (530 Wh/kg), both higher than reduced graphene oxide paper electrodes. Furthermore, addition of P3HT-b-PEO enhances lithium-ion diffusion, eliminates cracking during cycling, and boosts cyclability relative to V2O5 alone. These results highlight the importance of tradeoffs between mechanical and electrochemical performance, where polymer content can be used to tune both aspects.
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    Tannic Acid as a Small-Molecule Binder for Silicon Anodes
    (American Chemical Society, 2020) Sarang, Kasturi T.; Li, Xiaoyi; Miranda, Andrea; Terlier, Tanguy; Oh, Eun-Suok; Verduzco, Rafael; Lutkenhaus, Jodie L.
    Increasing demand for portable electronic devices, electric vehicles, and grid scale energy storage has spurred interest in developing high-capacity rechargeable lithium-ion batteries (LIBs). Silicon is an abundantly available anode material that has a theoretical gravimetric capacity of 3579 mAh/g and a low operating potential of 0–1 V vs Li/Li+. However, silicon suffers from large volume variation (>300%) during lithiation and delithiation that leads to pulverization, causing delamination from the current collector and battery failure. These issues may be improved by using a binder that hydrogen bonds with the silicon nanoparticle surface. Here, we demonstrate the use of tannic acid, a natural polyphenol, as a binder for silicon anodes in lithium-ion batteries. Whereas the vast majority of silicon anode binders are high molecular weight polymers, tannic acid is explored here as a small molecule binder with abundant hydroxyl (−OH) groups (14.8 mmol of OH/g of tannic acid). This allows for the specific evaluation of hydrogen-bonding interactions toward effective binder performance without the consideration of particle bridging that occurs otherwise with high molecular weight polymers. The resultant silicon electrodes demonstrated a capacity of 850 mAh/g for 200 cycles and a higher capacity when compared to electrodes fabricated by using high molecular weight polymers such as poly(acrylic acid), sodium alginate, and poly(vinylidene fluoride). This work demonstrates that a small molecule with high hydrogen-bonding capability can be used a binder and provides insights into the behavior of small molecule binders for silicon anodes.