2019
DOI: 10.1016/j.jelechem.2019.01.070
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Electrochemically driven evolution of Br-containing aqueous solution composition

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Cited by 20 publications
(14 citation statements)
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“…Figure 5 shows the charge-discharge curves obtained in the second cycle. The voltage curve vs. the capacity during the charging process shows a stepwise growth in the region of 0.07 A h, which is common for similar dependences of the bromine-water system equilibrium potential predicted earlier for the electrooxidation of the bromide anion to the bromate anion [25]. The discharge capacity of the AQBRFB was 0.29 A h, which corresponds to 67% of the theoretically available 0.43 Ah.…”
Section: Resultssupporting
confidence: 75%
See 1 more Smart Citation
“…Figure 5 shows the charge-discharge curves obtained in the second cycle. The voltage curve vs. the capacity during the charging process shows a stepwise growth in the region of 0.07 A h, which is common for similar dependences of the bromine-water system equilibrium potential predicted earlier for the electrooxidation of the bromide anion to the bromate anion [25]. The discharge capacity of the AQBRFB was 0.29 A h, which corresponds to 67% of the theoretically available 0.43 Ah.…”
Section: Resultssupporting
confidence: 75%
“…Nevertheless, t in the acidic supporting electrolyte had an excess capacity determine transition in LiBrO3. Therefore, the total capacity of the posolyte rem higher than in the negolyte, since each bromate molecule can be reduc transition and the AQDSH2 molecule can only be oxidized by releasing Figure 5 shows the charge-discharge curves obtained in the secon curve vs. the capacity during the charging process shows a stepwise g of 0.07 A h, which is common for similar dependences of the brominelibrium potential predicted earlier for the electrooxidation of the br bromate anion [25]. The discharge capacity of the AQBRFB was 0.29 sponds to 67% of the theoretically available 0.43 Ah.…”
Section: Resultsmentioning
confidence: 52%
“…The process of the oxidative transformation of a bromide solution, in particular up to the bromate one, has been extensively explored in the literature. Its first stage gives molecular bromine where the tribromide ion, Br 3 − , is present as an intermediate, in conformity with the thermodynamic analysis and experimental studies of the solution composition [52][53][54][55]. Even though thermodynamic analysis predicts a direct transition of Br 2 to bromate in the course of a further oxidation process, its multi-electron character excludes it as a direct electrode reaction.…”
Section: Introductionsupporting
confidence: 74%
“…Unless otherwise mentioned, the following conditions were used: 25 mL of negolyte (2,7-AQDS or AS mixture), 50 mL of posolyte (0.5 M Br 2 /3.5 M HBr, the discharge capacity of posolyte is intentionally excessive in order to prevent the appearance of corrosive molecular bromine even at fully charged state of the battery [ 52 ]), serpentine flow field, Nafion 211 membrane, electrolyte flow rate 100 mL min −1 .…”
Section: Methodsmentioning
confidence: 99%