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Non-Solvent Induced Phase Separation Enables Designer Redox Flow Battery Electrodes

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    Abstract

    Porous carbonaceous electrodes are performance-defining components in redox flow batteries (RFBs), where their properties impact the efficiency, cost, and durability of the system. The overarching challenge is to simultaneously fulfill multiple seemingly contradictory requirements-i.e., high surface area, low pressure drop, and facile mass transport-without sacrificing scalability or manufacturability. Here, non-solvent induced phase separation (NIPS) is proposed as a versatile method to synthesize tunable porous structures suitable for use as RFB electrodes. The variation of the relative concentration of scaffold-forming polyacrylonitrile to pore-forming poly(vinylpyrrolidone) is demonstrated to result in electrodes with distinct microstructure and porosity. Tomographic microscopy, porosimetry, and spectroscopy are used to characterize the 3D structure and surface chemistry. Flow cell studies with two common redox species (i.e., all-vanadium and Fe2+/3+ ) reveal that the novel electrodes can outperform traditional carbon fiber electrodes. It is posited that the bimodal porous structure, with interconnected large (>50 µm) macrovoids in the through-plane direction and smaller (<5 µm) pores throughout, provides a favorable balance between offsetting traits. Although nascent, the NIPS synthesis approach has the potential to serve as a technology platform for the development of porous electrodes specifically designed to enable electrochemical flow technologies.

    Original languageEnglish
    Article number2006716
    Number of pages10
    JournalAdvanced Materials
    Volume33
    Issue number16
    Early online date2 Mar 2021
    DOIs
    Publication statusPublished - 22 Apr 2021

    Bibliographical note

    © 2020 The Authors. Advanced Materials published by Wiley-VCH GmbH.

    Funding

    The authors acknowledge the support from MIT's Center for Materials Science and Engineering Shared Experimental Facilities, supported in part by the MRSEC Program of the National Science Foundation under Award No. DMR1419807 and the Institute for Soldier Nanotechnologies, sponsored by the U.S. Army Research Office. This work was performed in part at the Center for Nanoscale Systems (CNS), a member of the National Nanotechnology Coordinated Infrastructure Network (NNCI), which was supported by the National Science Foundation under NSF Award No. 1541959. CNS is part of Harvard University. Research by C.T.‐C.W., Y.‐M.C., and F.R.B. was supported by the Joint Center for Energy Storage Research (JCESR), an Energy Innovation Hub funded by the U.S. Department of Energy, Office of Science, Basic Energy Sciences. C.T.‐C.W. acknowledges a graduate fellowship through the National Science Foundation Graduate Research Fellowship Program under Grant No. 1122374. Any opinions, findings, and conclusions or recommendations expressed in this material are those of the authors and do not necessarily reflect the views of the National Science Foundation. The authors thank Julianna La Lane Machado for her investigation of earlier embodiments of the phase separated materials and Dr. Rodrigo Ortiz de la Morena for support in generating scientific illustrations. The authors acknowledge the contribution of Peter J. L. Lipman and Tiny M. W. G. M. Verhoeven who carried out MIP and XPS analysis of the samples, respectively. The authors would also like to thank H. Greg Lin for his assistance in collection of the XTM images. A.F.‐C. gratefully acknowledges the financial support from the Dutch Science Foundation under the Veni Award (No. 17324). The authors acknowledge the support from MIT's Center for Materials Science and Engineering Shared Experimental Facilities, supported in part by the MRSEC Program of the National Science Foundation under Award No. DMR1419807 and the Institute for Soldier Nanotechnologies, sponsored by the U.S. Army Research Office. This work was performed in part at the Center for Nanoscale Systems (CNS), a member of the National Nanotechnology Coordinated Infrastructure Network (NNCI), which was supported by the National Science Foundation under NSF Award No. 1541959. CNS is part of Harvard University. Research by C.T.-C.W., Y.-M.C., and F.R.B. was supported by the Joint Center for Energy Storage Research (JCESR), an Energy Innovation Hub funded by the U.S. Department of Energy, Office of Science, Basic Energy Sciences. C.T.-C.W. acknowledges a graduate fellowship through the National Science Foundation Graduate Research Fellowship Program under Grant No. 1122374. Any opinions, findings, and conclusions or recommendations expressed in this material are those of the authors and do not necessarily reflect the views of the National Science Foundation. The authors thank Julianna La Lane Machado for her investigation of earlier embodiments of the phase separated materials and Dr. Rodrigo Ortiz de la Morena for support in generating scientific illustrations. The authors acknowledge the contribution of Peter J. L. Lipman and Tiny M. W. G. M. Verhoeven who carried out MIP and XPS analysis of the samples, respectively. The authors would also like to thank H. Greg Lin for his assistance in collection of the XTM images. A.F.-C. gratefully acknowledges the financial support from the Dutch Science Foundation under the Veni Award (No. 17324).

    FundersFunder number
    National Science FoundationDMR1419807, 1541959
    U.S. Department of Energy
    Harvard University
    Nederlandse Organisatie voor Wetenschappelijk Onderzoek17324

      Keywords

      • energy storage
      • phase separation
      • porous electrodes
      • redox flow batteries

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