Quinone voltammetry for redox-flow battery applications

The electrochemical behaviour of octafluoro-9,10-anthroquinone is reported, motivated by the use of this lipophilic quinone as the negative electrode couple (anolyte) in redox flow battery applications. At low concentrations, the reduction mechanism is found to follow the classic EE process, expecte...
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Gespeichert in:

Autor*in:	Jones, Alexandra E. [verfasserIn] Ejigu, Andinet [verfasserIn] Wang, Bin [verfasserIn] Adams, Ralph W. [verfasserIn] Bissett, Mark A. [verfasserIn] Dryfe, Robert A.W. [verfasserIn]

Format:	E-Artikel
Sprache:	Englisch

Erschienen:	2022

Schlagwörter:	Quinones Redox flow batteries Voltammetry Organic electrochemistry

Übergeordnetes Werk:	Enthalten in: Journal of electroanalytical chemistry - New York, NY [u.a.] : Elsevier, 1959, 920
Übergeordnetes Werk:	volume:920

DOI / URN:	10.1016/j.jelechem.2022.116572

Katalog-ID:	ELV008321701

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520			\|a The electrochemical behaviour of octafluoro-9,10-anthroquinone is reported, motivated by the use of this lipophilic quinone as the negative electrode couple (anolyte) in redox flow battery applications. At low concentrations, the reduction mechanism is found to follow the classic EE process, expected for quinones in aprotic solution and both anionic species are stable on the voltammetric timescale. The reduction process is, however, strongly influenced by a number of factors, including the identity of the electrolyte cation. The dianion is also unstable on longer timescales, with a disproportionation mechanism affecting the stability of reduced products, even at potentials above the reduction potential of the mono-anion. An insoluble film is shown to form on the electrode surface, which gradually degrades the voltammetric response. Conclusions from the electrochemical data are supported by in situ EPR and ex situ NMR spectroscopy.
650		4	\|a Quinones
650		4	\|a Redox flow batteries
650		4	\|a Voltammetry
650		4	\|a Organic electrochemistry
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700	1		\|a Adams, Ralph W. \|e verfasserin \|4 aut
700	1		\|a Bissett, Mark A. \|e verfasserin \|4 aut
700	1		\|a Dryfe, Robert A.W. \|e verfasserin \|4 aut
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author_variant	a e j ae aej a e ae b w bw r w a rw rwa m a b ma mab r a d ra rad
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allfields	10.1016/j.jelechem.2022.116572 doi (DE-627)ELV008321701 (ELSEVIER)S1572-6657(22)00564-1 DE-627 ger DE-627 rda eng 540 620 DE-600 35.27 bkl Jones, Alexandra E. verfasserin aut Quinone voltammetry for redox-flow battery applications 2022 nicht spezifiziert zzz rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier The electrochemical behaviour of octafluoro-9,10-anthroquinone is reported, motivated by the use of this lipophilic quinone as the negative electrode couple (anolyte) in redox flow battery applications. At low concentrations, the reduction mechanism is found to follow the classic EE process, expected for quinones in aprotic solution and both anionic species are stable on the voltammetric timescale. The reduction process is, however, strongly influenced by a number of factors, including the identity of the electrolyte cation. The dianion is also unstable on longer timescales, with a disproportionation mechanism affecting the stability of reduced products, even at potentials above the reduction potential of the mono-anion. An insoluble film is shown to form on the electrode surface, which gradually degrades the voltammetric response. Conclusions from the electrochemical data are supported by in situ EPR and ex situ NMR spectroscopy. Quinones Redox flow batteries Voltammetry Organic electrochemistry Ejigu, Andinet verfasserin aut Wang, Bin verfasserin aut Adams, Ralph W. verfasserin aut Bissett, Mark A. verfasserin aut Dryfe, Robert A.W. verfasserin aut Enthalten in Journal of electroanalytical chemistry New York, NY [u.a.] : Elsevier, 1959 920 Online-Ressource (DE-627)302466533 (DE-600)1491150-4 (DE-576)098614797 1873-2569 nnns volume:920 GBV_USEFLAG_U SYSFLAG_U GBV_ELV SSG-OLC-PHA GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_150 GBV_ILN_151 GBV_ILN_224 GBV_ILN_370 GBV_ILN_602 GBV_ILN_702 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2027 GBV_ILN_2034 GBV_ILN_2038 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2056 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2118 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2190 GBV_ILN_2336 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4313 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4338 GBV_ILN_4393 35.27 Elektrochemische Analyse AR 920
spelling	10.1016/j.jelechem.2022.116572 doi (DE-627)ELV008321701 (ELSEVIER)S1572-6657(22)00564-1 DE-627 ger DE-627 rda eng 540 620 DE-600 35.27 bkl Jones, Alexandra E. verfasserin aut Quinone voltammetry for redox-flow battery applications 2022 nicht spezifiziert zzz rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier The electrochemical behaviour of octafluoro-9,10-anthroquinone is reported, motivated by the use of this lipophilic quinone as the negative electrode couple (anolyte) in redox flow battery applications. At low concentrations, the reduction mechanism is found to follow the classic EE process, expected for quinones in aprotic solution and both anionic species are stable on the voltammetric timescale. The reduction process is, however, strongly influenced by a number of factors, including the identity of the electrolyte cation. The dianion is also unstable on longer timescales, with a disproportionation mechanism affecting the stability of reduced products, even at potentials above the reduction potential of the mono-anion. An insoluble film is shown to form on the electrode surface, which gradually degrades the voltammetric response. Conclusions from the electrochemical data are supported by in situ EPR and ex situ NMR spectroscopy. Quinones Redox flow batteries Voltammetry Organic electrochemistry Ejigu, Andinet verfasserin aut Wang, Bin verfasserin aut Adams, Ralph W. verfasserin aut Bissett, Mark A. verfasserin aut Dryfe, Robert A.W. verfasserin aut Enthalten in Journal of electroanalytical chemistry New York, NY [u.a.] : Elsevier, 1959 920 Online-Ressource (DE-627)302466533 (DE-600)1491150-4 (DE-576)098614797 1873-2569 nnns volume:920 GBV_USEFLAG_U SYSFLAG_U GBV_ELV SSG-OLC-PHA GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_150 GBV_ILN_151 GBV_ILN_224 GBV_ILN_370 GBV_ILN_602 GBV_ILN_702 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2027 GBV_ILN_2034 GBV_ILN_2038 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2056 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2118 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2190 GBV_ILN_2336 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4313 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4338 GBV_ILN_4393 35.27 Elektrochemische Analyse AR 920
allfields_unstemmed	10.1016/j.jelechem.2022.116572 doi (DE-627)ELV008321701 (ELSEVIER)S1572-6657(22)00564-1 DE-627 ger DE-627 rda eng 540 620 DE-600 35.27 bkl Jones, Alexandra E. verfasserin aut Quinone voltammetry for redox-flow battery applications 2022 nicht spezifiziert zzz rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier The electrochemical behaviour of octafluoro-9,10-anthroquinone is reported, motivated by the use of this lipophilic quinone as the negative electrode couple (anolyte) in redox flow battery applications. At low concentrations, the reduction mechanism is found to follow the classic EE process, expected for quinones in aprotic solution and both anionic species are stable on the voltammetric timescale. The reduction process is, however, strongly influenced by a number of factors, including the identity of the electrolyte cation. The dianion is also unstable on longer timescales, with a disproportionation mechanism affecting the stability of reduced products, even at potentials above the reduction potential of the mono-anion. An insoluble film is shown to form on the electrode surface, which gradually degrades the voltammetric response. Conclusions from the electrochemical data are supported by in situ EPR and ex situ NMR spectroscopy. Quinones Redox flow batteries Voltammetry Organic electrochemistry Ejigu, Andinet verfasserin aut Wang, Bin verfasserin aut Adams, Ralph W. verfasserin aut Bissett, Mark A. verfasserin aut Dryfe, Robert A.W. verfasserin aut Enthalten in Journal of electroanalytical chemistry New York, NY [u.a.] : Elsevier, 1959 920 Online-Ressource (DE-627)302466533 (DE-600)1491150-4 (DE-576)098614797 1873-2569 nnns volume:920 GBV_USEFLAG_U SYSFLAG_U GBV_ELV SSG-OLC-PHA GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_150 GBV_ILN_151 GBV_ILN_224 GBV_ILN_370 GBV_ILN_602 GBV_ILN_702 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2027 GBV_ILN_2034 GBV_ILN_2038 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2056 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2118 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2190 GBV_ILN_2336 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4313 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4338 GBV_ILN_4393 35.27 Elektrochemische Analyse AR 920
allfieldsGer	10.1016/j.jelechem.2022.116572 doi (DE-627)ELV008321701 (ELSEVIER)S1572-6657(22)00564-1 DE-627 ger DE-627 rda eng 540 620 DE-600 35.27 bkl Jones, Alexandra E. verfasserin aut Quinone voltammetry for redox-flow battery applications 2022 nicht spezifiziert zzz rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier The electrochemical behaviour of octafluoro-9,10-anthroquinone is reported, motivated by the use of this lipophilic quinone as the negative electrode couple (anolyte) in redox flow battery applications. At low concentrations, the reduction mechanism is found to follow the classic EE process, expected for quinones in aprotic solution and both anionic species are stable on the voltammetric timescale. The reduction process is, however, strongly influenced by a number of factors, including the identity of the electrolyte cation. The dianion is also unstable on longer timescales, with a disproportionation mechanism affecting the stability of reduced products, even at potentials above the reduction potential of the mono-anion. An insoluble film is shown to form on the electrode surface, which gradually degrades the voltammetric response. Conclusions from the electrochemical data are supported by in situ EPR and ex situ NMR spectroscopy. Quinones Redox flow batteries Voltammetry Organic electrochemistry Ejigu, Andinet verfasserin aut Wang, Bin verfasserin aut Adams, Ralph W. verfasserin aut Bissett, Mark A. verfasserin aut Dryfe, Robert A.W. verfasserin aut Enthalten in Journal of electroanalytical chemistry New York, NY [u.a.] : Elsevier, 1959 920 Online-Ressource (DE-627)302466533 (DE-600)1491150-4 (DE-576)098614797 1873-2569 nnns volume:920 GBV_USEFLAG_U SYSFLAG_U GBV_ELV SSG-OLC-PHA GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_150 GBV_ILN_151 GBV_ILN_224 GBV_ILN_370 GBV_ILN_602 GBV_ILN_702 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2027 GBV_ILN_2034 GBV_ILN_2038 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2056 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2118 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2190 GBV_ILN_2336 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4313 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4338 GBV_ILN_4393 35.27 Elektrochemische Analyse AR 920
allfieldsSound	10.1016/j.jelechem.2022.116572 doi (DE-627)ELV008321701 (ELSEVIER)S1572-6657(22)00564-1 DE-627 ger DE-627 rda eng 540 620 DE-600 35.27 bkl Jones, Alexandra E. verfasserin aut Quinone voltammetry for redox-flow battery applications 2022 nicht spezifiziert zzz rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier The electrochemical behaviour of octafluoro-9,10-anthroquinone is reported, motivated by the use of this lipophilic quinone as the negative electrode couple (anolyte) in redox flow battery applications. At low concentrations, the reduction mechanism is found to follow the classic EE process, expected for quinones in aprotic solution and both anionic species are stable on the voltammetric timescale. The reduction process is, however, strongly influenced by a number of factors, including the identity of the electrolyte cation. The dianion is also unstable on longer timescales, with a disproportionation mechanism affecting the stability of reduced products, even at potentials above the reduction potential of the mono-anion. An insoluble film is shown to form on the electrode surface, which gradually degrades the voltammetric response. Conclusions from the electrochemical data are supported by in situ EPR and ex situ NMR spectroscopy. Quinones Redox flow batteries Voltammetry Organic electrochemistry Ejigu, Andinet verfasserin aut Wang, Bin verfasserin aut Adams, Ralph W. verfasserin aut Bissett, Mark A. verfasserin aut Dryfe, Robert A.W. verfasserin aut Enthalten in Journal of electroanalytical chemistry New York, NY [u.a.] : Elsevier, 1959 920 Online-Ressource (DE-627)302466533 (DE-600)1491150-4 (DE-576)098614797 1873-2569 nnns volume:920 GBV_USEFLAG_U SYSFLAG_U GBV_ELV SSG-OLC-PHA GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_150 GBV_ILN_151 GBV_ILN_224 GBV_ILN_370 GBV_ILN_602 GBV_ILN_702 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2027 GBV_ILN_2034 GBV_ILN_2038 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2056 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2118 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2190 GBV_ILN_2336 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4313 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4338 GBV_ILN_4393 35.27 Elektrochemische Analyse AR 920
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topic_facet	Quinones Redox flow batteries Voltammetry Organic electrochemistry
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author	Jones, Alexandra E.
spellingShingle	Jones, Alexandra E. ddc 540 bkl 35.27 misc Quinones misc Redox flow batteries misc Voltammetry misc Organic electrochemistry Quinone voltammetry for redox-flow battery applications
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topic	ddc 540 bkl 35.27 misc Quinones misc Redox flow batteries misc Voltammetry misc Organic electrochemistry
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title_full	Quinone voltammetry for redox-flow battery applications
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title_sort	quinone voltammetry for redox-flow battery applications
title_auth	Quinone voltammetry for redox-flow battery applications
abstract	The electrochemical behaviour of octafluoro-9,10-anthroquinone is reported, motivated by the use of this lipophilic quinone as the negative electrode couple (anolyte) in redox flow battery applications. At low concentrations, the reduction mechanism is found to follow the classic EE process, expected for quinones in aprotic solution and both anionic species are stable on the voltammetric timescale. The reduction process is, however, strongly influenced by a number of factors, including the identity of the electrolyte cation. The dianion is also unstable on longer timescales, with a disproportionation mechanism affecting the stability of reduced products, even at potentials above the reduction potential of the mono-anion. An insoluble film is shown to form on the electrode surface, which gradually degrades the voltammetric response. Conclusions from the electrochemical data are supported by in situ EPR and ex situ NMR spectroscopy.
abstractGer	The electrochemical behaviour of octafluoro-9,10-anthroquinone is reported, motivated by the use of this lipophilic quinone as the negative electrode couple (anolyte) in redox flow battery applications. At low concentrations, the reduction mechanism is found to follow the classic EE process, expected for quinones in aprotic solution and both anionic species are stable on the voltammetric timescale. The reduction process is, however, strongly influenced by a number of factors, including the identity of the electrolyte cation. The dianion is also unstable on longer timescales, with a disproportionation mechanism affecting the stability of reduced products, even at potentials above the reduction potential of the mono-anion. An insoluble film is shown to form on the electrode surface, which gradually degrades the voltammetric response. Conclusions from the electrochemical data are supported by in situ EPR and ex situ NMR spectroscopy.
abstract_unstemmed	The electrochemical behaviour of octafluoro-9,10-anthroquinone is reported, motivated by the use of this lipophilic quinone as the negative electrode couple (anolyte) in redox flow battery applications. At low concentrations, the reduction mechanism is found to follow the classic EE process, expected for quinones in aprotic solution and both anionic species are stable on the voltammetric timescale. The reduction process is, however, strongly influenced by a number of factors, including the identity of the electrolyte cation. The dianion is also unstable on longer timescales, with a disproportionation mechanism affecting the stability of reduced products, even at potentials above the reduction potential of the mono-anion. An insoluble film is shown to form on the electrode surface, which gradually degrades the voltammetric response. Conclusions from the electrochemical data are supported by in situ EPR and ex situ NMR spectroscopy.
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title_short	Quinone voltammetry for redox-flow battery applications
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doi_str	10.1016/j.jelechem.2022.116572
up_date	2024-07-06T19:18:10.706Z
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Quinone voltammetry for redox-flow battery applications

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