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Efficient charge transport pathways in solutions of redox-active polymers are essential for advancing nextgeneration energy storage systems. Herein, we report the grafting of (2,2,6,6-tetramethylpiperidin-1-yl)oxyl (TEMPO) and poly(2,2,6,6-tetramethyl-1-piperidinyloxy-4-yl methacrylate) (PTMA) polymer brushes onto silica particles with different molecular weights and grafting densities, and the impact of these composite particles in solutions of PTMA. The polymer-grafted particles are characterized using Fourier-transform infrared (FTIR) spectroscopy, X-ray photoelectron spectroscopy (XPS), electron paramagnetic resonance (EPR) spectroscopy, field emission scanning electron microscopy (FESEM), transmission electron microscopy (TEM), and dynamic light scattering (DLS) techniques. The grafted polymers have molecular weights of 2.5 kDa and 5.0 kDa, with corresponding grafting densities of 0.688 and 0.378 chains nm−2 for SiO2-PTMA-2.5k and SiO2-PTMA-5k, respectively, with the grafting density decreasing with increasing graft length. To investigate the effect of these composite particles on charge transport in solutions of PTMA, different concentrations of the grafted particles were added to solutions of PTMA of different concentrations (near overlap concentration, C*) in 0.1 M LiTFSI in acetonitrile. Electrochemical analysis reveals that below C* the addition of SiO2-PTMA-5k increases the apparent diffusion coefficient (Dapp) 15.2% to 1.041 × 10−6 cm2 s−1 , the exchange rate constant (kex,app) by 9.5% to 1.546 × 1011 L mol−1 s−1, and the heterogeneous electron transfer rate constant (k0) by 24.6%, to 5.526 × 10−4 cm s−1. These results indicate that the synergistic interactions between unbound PTMA polymer chains in solution and PTMA-grafted particles facilitate interchain charge transfer kinetics. This highlights that grafted redoxactive particles can enhance charge transport without the limitations of polymer-only solutions (e.g., chain entanglement) and presents a promising design strategy for high-performance electrochemical applications, such as redox flow batteries (RFBs).
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Recyclable Organic Radical Electrodes for Metal‐Free Batteries
Abstract Organic batteries are one of the possible routes for transitioning to sustainable energy storage solutions. However, the recycling of organic batteries, which is a key step toward circularity, is not easily achieved. This work shows the direct recycling of poly(2,2,6,6‐tetramethylpiperidinyloxy‐4‐yl) (PTMA) and poly(2,2,6,6‐tetramethylpiperidinyloxy‐4‐yl acrylamide) (PTAm) based composite electrodes. After charge‐discharge cycling, the electrodes are deconstructed using a solubilizing‐solvent and then reconstructed using a casting‐solvent. The electrochemical properties of the original and recycled electrodes are compared using cyclic voltammetry (CV) and galvanostatic charge‐discharge (GCD) cycling, from which it is discovered using time‐of‐flight secondary ion mass spectrometry (ToF‐SIMS) that recycling can be challenged by the formation of a cathode electrolyte interphase (CEI). In turn, an additive is proposed to modify the CEI layer and improve the properties after recycling. Last, an anionic rocking chair battery consisting of PTAm electrodes as both positive and negative electrodes is demonstrated, in which the electrodes are recycled to form a new battery. This work demonstrates the recycling of composite electrodes for organic batteries and provides insights into the challenges and possible solutions for recycling the next‐generation electrochemical energy storage devices.
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- Award ID(s):
- 2104179
- PAR ID:
- 10513943
- Publisher / Repository:
- Wiley Blackwell (John Wiley & Sons)
- Date Published:
- Journal Name:
- ChemSusChem
- Volume:
- 17
- Issue:
- 20
- ISSN:
- 1864-5631
- Format(s):
- Medium: X
- Sponsoring Org:
- National Science Foundation
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