4.6 Article

Redox-Active Polymers Designed for the Circular Economy of Energy Storage Devices

Journal

ACS ENERGY LETTERS
Volume 6, Issue 10, Pages 3450-3457

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acsenergylett.1c01625

Keywords

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Funding

  1. TomKat Center for Sustainable Energy at Stanford University
  2. National Science Foundation Award CBET [1804915]
  3. NSF [DGE-1656518]
  4. National Science Foundation as part of the National Nanotechnology Coordinated Infrastructure [ECCS-1542152]
  5. Office of Sponsored Research (OSR) [OSR-2018-CRG/CCF-3079, OSR-2019-CRG8-4086, OSR-2018-CRG7-3749]
  6. ERC [610115]
  7. U.S. Department of Energy, Office of Science, Office of Basic Energy Sciences [DE-AC02-76SF00515]
  8. KAUST
  9. Directorate For Engineering
  10. Div Of Chem, Bioeng, Env, & Transp Sys [1804915] Funding Source: National Science Foundation

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This study demonstrates recyclable energy storage devices based on solution-processable redox-active conjugated polymers, achieving high performance and electrochemical stability through high electronic and ionic charge transport. The devices are able to retain over 85% of capacity in multiple recycling steps, providing a new framework for recyclability in sustainable energy storage technologies.
Electrochemical energy storage is a keystone to support the rapid transition to a low-carbon-emission future for grid storage and transportation. While research on electrochemical energy storage devices has mostly dealt with performance improvements (energy density and power density), little attention has been paid to designing devices that can be recycled with low cost and low environmental impact. Thus, next-generation energy storage devices should also address the integration of recyclability into the device design. Here, we demonstrate recyclable energy storage devices based on solution-processable redox-active conjugated polymers. The high electronic and ionic charge transport in these polymers enables the operation of single-phase electrodes in aqueous electrolytes with C-rates >100 with good electrochemical stability when the cell is charged to 1.2 V. Finally, we demonstrate the recyclability of these devices, achieving >85% capacity retention in each recycling step. Our work provides a framework for developing recyclable devices for sustainable energy storage technologies.

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