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Carbon disulfide: A redox mediator for organodisulfides in redox flow batteries.

Qiliang ChenWenmin WangXin LiWei GuoYongzhu Fu
Published in: Proceedings of the National Academy of Sciences of the United States of America (2022)
Organodisulfides (RSSR) are a class of promising active materials for redox flow batteries (RFBs). However, their sluggish kinetics and poor cyclic stability remain a formidable challenge. Here, we propose carbon disulfide (CS 2 ) as a unique redox mediator involving reversible C-S bond formation/breakage to facilitate the reduction reaction of organodisulfides in RFBs. In the discharge of RSSR, CS 2 interacts with the negatively charged RSSR -• to promote cleavage of the S-S bond by reducing about one-third of the energy barrier, forming RSCS 2 Li. In the recharge, CS 2 is unbonded from RSCS 2 Li while RSSR is regenerated. Meanwhile, the redox mediator can also be inserted into the molecular structure of RSSR to form RSCS 2 SR/RSCS 2 CS 2 SR, and these new active materials with lower energy barriers can further accelerate the reaction kinetics of RSSR. With CS 2 , phenyl disulfide exhibits an exceptional rate capability and cyclability of 500 cycles. An average energy efficiency of >90% is achieved. This strategy provides a unique redox-mediating pathway involving C-S bond formation/breakage with the active species, which is different from those used in lithium-oxygen or other batteries.
Keyphrases
  • electron transfer
  • solid state
  • single molecule
  • ion batteries