TY - JOUR
T1 - Alkaline aqueous organic redox flow batteries of high energy and power densities using mixed naphthoquinone derivatives
AU - Lee, Wonmi
AU - Park, Gyunho
AU - Kwon, Yongchai
N1 - Publisher Copyright:
© 2019 Elsevier B.V.
PY - 2020/4/15
Y1 - 2020/4/15
N2 - Mixture of 1,2-naphthoquinone-4-sulfonic acid sodium salt (NQ-S) and 2-hydroxy-1,4-naphthoquinone (Lawsone) is used as negative active species for aqueous organic redox flow battery (AORFB), while ferrocyanide (FeCN) is considered as positive active species in alkaline electrolyte. NQ-S is initially transformed to NQ-OH that has the same chemical structure with Lawsone by the nucleophilic attack under potassium hydroxide (KOH) electrolyte. The mixture of NQ-S and Lawsone (NQ-SO) has a higher solubility in KOH electrolyte (1.26 M in 1 M KOH) than the individual NQ-SO and NQ-S (0.42 and 0.83 M in 1 M KOH, respectively) because of the hydrophilic sulfite (–SO32−) groups eliminated from NQ-S over the transformation and the polar-polar interaction amid –SO32− group, organic species and KOH electrolyte. Lawsone to NQ-S ratio for optimal NQ-SO is 2:1, and this ratio is determined by the hygroscopic properties of –SO32− group. The cell voltage of AORFB using 0.6 M NQ-SO and 0.4 M FeCN is 1.01 V and its charge efficiency, discharge capacity, state of charge (SOC) and power density under 100 mA∙cm−2 are 99%, 23 Ah·L−1, 70% and 90 mW·cm−2. Furthermore, when the concentration of NQ-SO increases to 1.2 M (AORFB using 1.2 M NQ-SO and 0.4 M FeCN), its discharge capacity considerably increased to 40.3 Ah·L−1 with SOC of 83% and power density of 72 mW·cm−2.
AB - Mixture of 1,2-naphthoquinone-4-sulfonic acid sodium salt (NQ-S) and 2-hydroxy-1,4-naphthoquinone (Lawsone) is used as negative active species for aqueous organic redox flow battery (AORFB), while ferrocyanide (FeCN) is considered as positive active species in alkaline electrolyte. NQ-S is initially transformed to NQ-OH that has the same chemical structure with Lawsone by the nucleophilic attack under potassium hydroxide (KOH) electrolyte. The mixture of NQ-S and Lawsone (NQ-SO) has a higher solubility in KOH electrolyte (1.26 M in 1 M KOH) than the individual NQ-SO and NQ-S (0.42 and 0.83 M in 1 M KOH, respectively) because of the hydrophilic sulfite (–SO32−) groups eliminated from NQ-S over the transformation and the polar-polar interaction amid –SO32− group, organic species and KOH electrolyte. Lawsone to NQ-S ratio for optimal NQ-SO is 2:1, and this ratio is determined by the hygroscopic properties of –SO32− group. The cell voltage of AORFB using 0.6 M NQ-SO and 0.4 M FeCN is 1.01 V and its charge efficiency, discharge capacity, state of charge (SOC) and power density under 100 mA∙cm−2 are 99%, 23 Ah·L−1, 70% and 90 mW·cm−2. Furthermore, when the concentration of NQ-SO increases to 1.2 M (AORFB using 1.2 M NQ-SO and 0.4 M FeCN), its discharge capacity considerably increased to 40.3 Ah·L−1 with SOC of 83% and power density of 72 mW·cm−2.
KW - Alkaline supporting electrolyte
KW - Aqueous organic redox flow battery
KW - Ferrocyanide
KW - Mixed naphthoquinone
KW - Nucleophilic attack
UR - http://www.scopus.com/inward/record.url?scp=85077330894&partnerID=8YFLogxK
U2 - 10.1016/j.cej.2019.123985
DO - 10.1016/j.cej.2019.123985
M3 - Article
AN - SCOPUS:85077330894
SN - 1385-8947
VL - 386
JO - Chemical Engineering Journal
JF - Chemical Engineering Journal
M1 - 123985
ER -