TY - JOUR
T1 - Organometallic redox flow batteries using iron triethanolamine and cobalt triethanolamine complexes
AU - Noh, Chanho
AU - Chung, Yongjin
AU - Kwon, Yongchai
N1 - Publisher Copyright:
© 2020 Elsevier B.V.
PY - 2020/8/1
Y1 - 2020/8/1
N2 - Organometallic complexes consisting of iron- and cobalt-triethanolamine ligand (Fe (TEA) and Co(TEA)) are proposed as redox couple of aqueous redox flow battery (ARFB). Fe (TEA) and Co(TEA) are dissolved in sodium hydroxide (NaOH) electrolyte, while their chemical stability and electrochemical reactivity are quantitatively characterized. As a result, the chemical stability of Co(TEA) is degraded for multiple charge/discharge cycle test due to the deformation of unchelated TEAs by the chemical reaction with hydroxyl ion (OH−) and the catalytic effect of Co(TEA). To address the issue, the ratio of Co to TEA and the concentration of NaOH are manipulated. When the ratio is 1:1, the redox reactivity of Co(TEA) is improved because the amount of unchelated TEAs that is a reason for lowering its redox reactivity is minimized, while 4 M NaOH is proper to supply enough amount of OH−, preserving its chemical structure and reducing mass transfer retardation. Regarding Fe (TEA), with 1:2.5 ratio of Fe to TEA in 4 M NaOH, the stability and performance of Fe (TEA) are best. Performance of ARFB using 1:2.5 Fe (TEA) and 1:1 Co(TEA) shows excellent results of high charge and energy efficiencies of 99% and 62% at 40 mA cm−2, and high power density of 35 mWcm−2.
AB - Organometallic complexes consisting of iron- and cobalt-triethanolamine ligand (Fe (TEA) and Co(TEA)) are proposed as redox couple of aqueous redox flow battery (ARFB). Fe (TEA) and Co(TEA) are dissolved in sodium hydroxide (NaOH) electrolyte, while their chemical stability and electrochemical reactivity are quantitatively characterized. As a result, the chemical stability of Co(TEA) is degraded for multiple charge/discharge cycle test due to the deformation of unchelated TEAs by the chemical reaction with hydroxyl ion (OH−) and the catalytic effect of Co(TEA). To address the issue, the ratio of Co to TEA and the concentration of NaOH are manipulated. When the ratio is 1:1, the redox reactivity of Co(TEA) is improved because the amount of unchelated TEAs that is a reason for lowering its redox reactivity is minimized, while 4 M NaOH is proper to supply enough amount of OH−, preserving its chemical structure and reducing mass transfer retardation. Regarding Fe (TEA), with 1:2.5 ratio of Fe to TEA in 4 M NaOH, the stability and performance of Fe (TEA) are best. Performance of ARFB using 1:2.5 Fe (TEA) and 1:1 Co(TEA) shows excellent results of high charge and energy efficiencies of 99% and 62% at 40 mA cm−2, and high power density of 35 mWcm−2.
KW - Aqueous redox flow battery
KW - Cobalt and iron
KW - Energy storage system
KW - Organometallic complex
KW - Triethanolamine chelate
UR - http://www.scopus.com/inward/record.url?scp=85084546777&partnerID=8YFLogxK
U2 - 10.1016/j.jpowsour.2020.228333
DO - 10.1016/j.jpowsour.2020.228333
M3 - Article
AN - SCOPUS:85084546777
SN - 0378-7753
VL - 466
JO - Journal of Power Sources
JF - Journal of Power Sources
M1 - 228333
ER -