Electrochemical evaluation methods of vanadium flow battery electrodes

Literature Information

Publication Date 2017-05-09
DOI 10.1039/C7CP02581E
Impact Factor 3.676
Authors

Lantao Wu, Jianshe Wang, Yi Shen, Le Liu, Jingyu Xi


View Original

Abstract

Various testing methods, such as cyclic voltammetry (CV) and electrochemical impedance spectroscopy (EIS), have been employed to evaluate the electrode performance of vanadium flow batteries (VFB). Due to the variations in the testing devices and characterization parameters in the literature, a number of reported results are incomparable and even sometimes contradictory. In this report, a reliable device is proposed for the electrochemical characterization of electrode materials, and the parameter selection was demonstrated to be critical for achieving reliable evaluation and reducing the effects of side reactions. As for the structure of the graphite felt electrode, volume current density is proposed to replace the area current density as the main evaluation indicator. Furthermore, the effect of side reactions is discussed and the upper limit voltage of 1.60 V is found to be suitable in the charge process of VFB since selecting this value can greatly protect the active sites on the electrode and avoid the capacity fading caused by side reactions.

Related Literature

Homolysis/mesolysis of alkoxyamines activated by chemical oxidation and photochemical-triggered radical reactions at room temperature

Gérard Audran, Mitchell T. Blyth, Michelle L. Coote, Georg Gescheidt, Micael Hardy, Jeffrey Havot, Maxence Holzritter, Samuel Jacoutot, Jean-Patrick Joly, Sylvain R. A. Marque, Tataye Moussounda Moussounda Koumba, Dmytro Neshchadin, Enzo Vaiedelich

2021-10-14 Research Article

DOI: 10.1039/D1QO01276B

Divergent synthesis of new α-glucosidase inhibitors obtained through a vinyl Grignard-mediated carbocyclisation

Ida M. B. Knudsen, Christinne Hedberg, Daisuke Ide, Anne Brinkø, Espen Z. Eikeland, Atsushi Kato, Henrik H. Jensen

2018-08-07 Paper

DOI: 10.1039/C8OB01433G

Ruthenium-catalyzed C–H allylation of arenes with allylic amines

Rui Yan

2018-05-07 Paper

DOI: 10.1039/C8OB00723C

Nickel catalyzed site selective C–H functionalization of α-aryl-thioamides

Debashruti Bandyopadhyay, Annaram Thirupathi, Nagsen Munjaji Dhage, Nirmala Mohanta, S. Peruncheralathan

2018-08-23 Communication

DOI: 10.1039/C8OB01712C

2-Pyridinylmethyl borrowing: base-promoted C-alkylation of (pyridin-2-yl)-methyl alcohols with ketones via cleavage of unstrained C(sp3)–C(sp3) bonds

Chuan-Ming Hong, Fei-Fei Zou, Xin Zhuang, Zhen Luo, Zheng-Qiang Liu, Li-Qing Ren, Qing-Hua Li, Tang-Lin Liu

2021-11-23 Research Article

DOI: 10.1039/D1QO01446C

High pressure-assisted low-loading asymmetric organocatalytic conjugate addition of nitroalkanes to chalcones‡

Agnieszka Cholewiak, Kamil Adamczyk, Michał Kopyt, Adrian Kasztelan, Piotr Kwiatkowski

2018-05-22 Paper

DOI: 10.1039/C8OB00561C

Unexpected cyclization of 2-(2-aminophenyl)indoles with nitroalkenes to furnish indolo[3,2-c]quinolines

Alexander V. Aksenov, Dmitrii A. Aksenov, Nicolai A. Aksenov, Leonid G. Voskressensky

2018-05-22 Paper

DOI: 10.1039/C8OB00588E

Efficient enantioselective synthesis of CF2H-containing dispiro[benzo[b]thiophene-oxindole-pyrrolidine]s via organocatalytic cycloaddition

Yabo Deng, Yongzhen Li, Yalan Wang, Shuo Sun, Sichao Ma, Pengfei Jia, Wenguang Li, Kairong Wang, Wenjin Yan

2021-11-24 Research Article

DOI: 10.1039/D1QO01392K

gem-Difluorovinylation of alkynyl bromoarenes via dual nickel-/palladium-catalyzed cross-electrophile coupling

Haotian Sun, Baojian Xiong, Yuan Yang, Jiangjun Liu, Xuemei Zhang, Zhong Lian

2021-11-23 Research Article

DOI: 10.1039/D1QO01406D

Caged cyclopropenes for controlling bioorthogonal reactivity

Pratik Kumar, Ting Jiang, Sining Li, Omar Zainul, Scott T. Laughlin

2018-05-16 Communication

DOI: 10.1039/C8OB01076E

You might also like

Compound Q&A

What industries use (1R,3S)-1,3-Cyclopentanediol (CAS: 16326-97-9)?

(1R,3S)-1,3-Cyclopentanediol finds applications in various industries. In the ph...

16326-97-9(1R,3S)-1,3-Cyclopen...
Compound Q&A

What precautions should be taken when handling N'-[4-(Dimethylamino)phenyl]-N,N-dimethyl-1,4-benzenediamine (CAS: 637-31-0)?

When handling N'-[4-(Dimethylamino)phenyl]-N,N-dimethyl-1,4-benzenediamine, it i...

637-31-0N'-[4-(Dimethylamino...
Compound Q&A

Are there alternatives to 5-(2,4-Difluorophenyl)-2-methoxypyrimidine (CAS: 1352318-16-1) in synthesis?

There are several alternatives to 5-(2,4-Difluorophenyl)-2-methoxypyrimidine in ...

1352318-16-15-(2,4-Difluoropheny...
Compound Q&A

What regulatory guidelines apply to 1-(3-Methoxyphenoxy)propan-2-ol (CAS: 382141-68-6)?

1-(3-Methoxyphenoxy)propan-2-ol (CAS: 382141-68-6) must comply with the Globally...

382141-68-61-(3-Methoxyphenoxy)...
Compound Q&A

Is Tetrodotoxin Citrate (CAS: 18660-81-6) safe?

Tetrodotoxin Citrate is extremely dangerous and should be handled with extreme c...

18660-81-6Tetrodotoxin Citrate
Compound Q&A

What are the main uses of 2-Methyl-2-propanyl [(1R,3S)-3-hydroxycyclopentyl]carbamate (CAS: 225641-84-9)?

2-Methyl-2-propanyl [(1R,3S)-3-hydroxycyclopentyl]carbamate (CAS: 225641-84-9) i...

225641-84-92-Methyl-2-propanyl ...
Compound Q&A

How should waste containing 4-(2-Hydroxyhexafluoroisopropyl)Benzoic Acid (CAS: 16261-80-6) be handled?

Waste containing 4-(2-Hydroxyhexafluoroisopropyl)Benzoic Acid (CAS: 16261-80-6) ...

16261-80-64-(2-Hydroxyhexafluo...
Compound Q&A

How is 2-Methyl-2-proanyl {(2S)-1-[(benzyloxy)amino]-3-hydroxy-3-methyl-1-oxo-2-butanyl}carbamate (CAS: 102507-19-7) typically synthesized?

2-Methyl-2-proanyl {(2S)-1-[(benzyloxy)amino]-3-hydroxy-3-methyl-1-oxo-2-butanyl...

102507-19-72-Methyl-2-propanyl ...
Compound Q&A

What is Benzeneethanamine, α-ethyl-, hydrochloride (1:1) (CAS: 20735-15-3)?

Benzeneethanamine, α-ethyl-, hydrochloride (1:1) is an organic compound with the...

20735-15-3Benzeneethanamine, α...
Compound Q&A

Are there alternatives to 3-{(E)-[4-(Dimethylamino)phenyl]diazenyl}benzoic acid (CAS: 20691-84-3) in synthesis?

In the synthesis of compounds similar to 3-{(E)-[4-(Dimethylamino)phenyl]diazeny...

20691-84-33-{(E)-[4-(Dimethyla...

Source Journal

Physical Chemistry Chemical Physics

Physical Chemistry Chemical Physics
CiteScore: 5.5
Self-citation Rate: 10.3%
Articles per Year: 3036

Physical Chemistry Chemical Physics (PCCP) is an international journal co-owned by 19 physical chemistry and physics societies from around the world. This journal publishes original, cutting-edge research in physical chemistry, chemical physics and biophysical chemistry. To be suitable for publication in PCCP, articles must include significant innovation and/or insight into physical chemistry; this is the most important criterion that reviewers and Editors will judge against when evaluating submissions. The journal has a broad scope and welcomes contributions spanning experiment, theory, computation and data science. Topical coverage includes spectroscopy, dynamics, kinetics, statistical mechanics, thermodynamics, electrochemistry, catalysis, surface science, quantum mechanics, quantum computing and machine learning. Interdisciplinary research areas such as polymers and soft matter, materials, nanoscience, energy, surfaces/interfaces, and biophysical chemistry are welcomed if they demonstrate significant innovation and/or insight into physical chemistry. Joined experimental/theoretical studies are particularly appreciated when complementary and based on up-to-date approaches.

Recommended Compounds

Recommended Suppliers

Disclaimer
This page provides academic journal information for reference and research purposes only. We are not affiliated with any journal publishers and do not handle publication submissions. For publication-related inquiries, please contact the respective journal publishers directly.
If you notice any inaccuracies in the information displayed, please contact us at support@chemtradehub.com. We will promptly review and address your concerns.