Redox-Active Polymers Designed for the Circular Economy of Energy Storage Devices
Name:
images_large_nz1c01625_0004.jpeg
Size:
97.11Kb
Format:
JPEG image
Description:
Graphical abstract
Type
ArticleAuthors
Tan, Siew Ting Melissa
Quill, Tyler J.

Moser, Maximilian

LeCroy, Garrett
Chen, Xingxing

Wu, Yilei

Takacs, Christopher J.
Salleo, Alberto
Giovannitti, Alexander

KAUST Grant Number
OSR-2018-CRG/CCF-3079OSR-2018-CRG7-3749
OSR-2019-CRG8-4086
Date
2021-09-08Online Publication Date
2021-09-08Print Publication Date
2021-10-08Embargo End Date
2022-09-08Submitted Date
2021-08-03Permanent link to this record
http://hdl.handle.net/10754/671136
Metadata
Show full item recordAbstract
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.Citation
Tan, S. T. M., Quill, T. J., Moser, M., LeCroy, G., Chen, X., Wu, Y., … Giovannitti, A. (2021). Redox-Active Polymers Designed for the Circular Economy of Energy Storage Devices. ACS Energy Letters, 3450–3457. doi:10.1021/acsenergylett.1c01625Sponsors
A.G. and A.S. acknowledge funding from the TomKat Center for Sustainable Energy at Stanford University and the StorageX initiative. A.S. and S.T.M.T. gratefully acknowledge support from the National Science Foundation Award CBET #1804915. T.J.Q. and G.L. acknowledge support from the NSF Graduate Research Fellowship Program under grant DGE-1656518. Part of this work was performed at the Stanford Nanofabrication Facilities (SNF) and Stanford Nano Shared Facilities (SNSF), supported by the National Science Foundation as part of the National Nanotechnology Coordinated Infrastructure under award ECCS-1542152. The authors acknowledge financial support from KAUST, including the Office of Sponsored Research (OSR) award nos. OSR-2018-CRG/CCF-3079, OSR-2019-CRG8-4086, and OSR-2018-CRG7-3749. The authors acknowledge funding from an ERC Synergy Grant SC2 (610115). Use of the Stanford Synchrotron Radiation Lightsource, SLAC National Accelerator Laboratory, is supported by the U.S. Department of Energy, Office of Science, Office of Basic Energy Sciences, under Contract No. DE-AC02-76SF00515.Publisher
American Chemical Society (ACS)Journal
ACS Energy LettersAdditional Links
https://pubs.acs.org/doi/10.1021/acsenergylett.1c01625https://www.osti.gov/biblio/1873513
ae974a485f413a2113503eed53cd6c53
10.1021/acsenergylett.1c01625