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Synthesis and Characterization of Redox-Responsive Disulfide Cross-Linked Polymer Particles for Energy Storage Applications
Author(s) -
Garrett L. Grocke,
Hongyi Zhang,
Samuel S. Kopfinger,
Shrayesh N. Patel,
Stuart J. Rowan
Publication year - 2021
Publication title -
acs macro letters
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.966
H-Index - 92
ISSN - 2161-1653
DOI - 10.1021/acsmacrolett.1c00682
Subject(s) - redox , electrochemistry , materials science , polymer , electrolyte , chemical engineering , particle size , energy storage , particle (ecology) , polymer chemistry , combinatorial chemistry , chemistry , electrode , power (physics) , physics , oceanography , quantum mechanics , engineering , metallurgy , composite material , geology
Cross-linking poly(glycidyl methacrylate) microparticles with redox-responsive bis(5-amino-l,3,4-thiadiazol-2-yl) disulfide moieties yield redox-active particles (RAPs) capable of electrochemical energy storage via a reversible 2-electron reduction of the disulfide bond. The resulting RAPs show improved electrochemical reversibility compared to a small-molecule disulfide analogue in solution, attributed to spatial confinement of the polymer-grafted disulfides in the particle. Galvanostatic cycling was used to investigate the impact of electrolyte selection on stability and specific capacity. A dimethyl sulfoxide/magnesium triflate electrolyte was ultimately selected for its favorable electrochemical reversibility and specific capacity. Additionally, the specific capacity showed a strong dependence on particle size where smaller particles yielded higher specific capacity. Overall, these experiments offer a promising direction in designing synthetically facile and electrochemically stable materials for organosulfur-based multielectron energy storage coupled with beyond Li ion systems such as Mg.

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