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Dithiolene Complexes of First‐Row Transition Metals for Symmetric Nonaqueous Redox Flow Batteries
Author(s) -
Hogue Ross W.,
Armstrong Craig G.,
Toghill Kathryn E.
Publication year - 2019
Publication title -
chemsuschem
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.412
H-Index - 157
eISSN - 1864-564X
pISSN - 1864-5631
DOI - 10.1002/cssc.201901702
Subject(s) - redox , chemistry , transition metal , electrolyte , metal , inorganic chemistry , electrode , catalysis , organic chemistry
Abstract Five metal complexes of the dithiolene ligand maleonitriledithiolate (mnt 2− ) with M=V, Fe, Co, Ni, Cu were studied as redox‐active materials for nonaqueous redox flow batteries (RFBs). All five complexes exhibit at least two redox processes, making them applicable to symmetric RFBs as single‐species electrolytes, that is, as both negolyte and posolyte. Charge–discharge cycling in a small‐scale RFB gave modest performances for [(tea) 2 V mnt ], [(tea) 2 Co mnt ], and [(tea) 2 Cu mnt ] whereas [(tea)Fe mnt ] and [(tea) 2 Ni mnt ] (tea=tetraethylammonium) failed to hold any significant capacity, indicating poor stability. Independent negolyte‐ and posolyte‐only battery cycling of a single redox couple, as well as UV/Vis spectroscopy, showed that for [(tea) 2 V mnt ] the negolyte is stable whereas the posolyte is unstable over multiple charge–discharge cycles; for [(tea) 2 Co mnt ], [(tea) 2 Ni mnt ], and [(tea) 2 Cu mnt ], the negolyte suffers rapid capacity fading although the posolyte is more robust. Identifying a means to stabilize V mnt 3−/2− as a negolyte, and Co mnt 2−/1− , Ni mnt 2−/1− , and Cu mnt 2−/1− as posolytes could lead to their use in asymmetric RFBs.