High-energy and high-power Zn–Ni flow batteries with semi-solid electrodes
Literature Information
Yun Guang Zhu, Thaneer Malai Narayanan, Michal Tulodziecki, Hernan Sanchez-Casalongue, Quinn C. Horn, Laura Meda, Yang Yu, Jame Sun, Tom Regier, Gareth H. McKinley
Flow battery technology offers a promising low-cost option for stationary energy storage applications. Aqueous zinc–nickel battery chemistry is intrinsically safer than non-aqueous battery chemistry (e.g. lithium-based batteries) and offers comparable energy density. In this work, we show how combining high power density and low-yield stress electrodes can minimize energy loss due to pumping, and have demonstrate methods to achieve high energy and power density for ZnO/Ni(OH)2 electrodes by changing composition and optimizing testing protocols. Firstly, mechanically stable and homogeneous Ni(OH)2/carbon and ZnO/Zn flowable electrodes in 7 M KOH electrolyte were designed using a microgel dispersion as the suspending matrix. By determining the critical volume fractions for conductivity percolation, colloidal suspensions with 6.2 vol% of carbon and 23.1 vol% of Zn were selected for preparing catholytes and anolytes to ensure that these semi-solid electrodes possess high voltage and high coulombic efficiencies. The resulting flowable electrodes exhibited non-Newtonian rheology with a yield stress of approximately ∼200 Pa, which assists in maintaining mechanical stability of the suspensions. An energy density of up to 134 W h Lcatholyte−1 and power density up to ∼159 mW cmgeo.−2 was demonstrated for semi-solid ZnO/Ni(OH)2 electrodes, and coulombic efficiency of 94% was achieved during cycling by optimizing the charging protocol to 60% SOC of Ni(OH)2. Lastly, semi-solid ZnO and Ni(OH)2 flow cells were built and tested using an intermittent mode of operation. The high energy and power densities, high coulombic efficiency, and negligible pumping loss of the Zn–Ni semi-solid electrodes developed in the present work present a promising system for further development.
Related Literature
Molecular dynamics of anhydrous glycolipid self-assembly in lamellar and hexagonal phases
T. S. Velayutham, B. K. Ng, W. C. Gan, V. Manickam Achari, N. I. Zahid, W. H. Abd. Majid, C. Zannoni, R. Hashim
DOI: 10.1039/C6CP00583G
Salt effects on the picosecond dynamics of lysozyme hydration water investigated by terahertz time-domain spectroscopy and an insight into the Hofmeister series for protein stability and solubility
Katsuyoshi Aoki, Kentaro Shiraki, Toshiaki Hattori
DOI: 10.1039/C5CP06324H
Synthesis, photophysical, electrochemical and electrochemiluminescence properties of A2B2 zinc porphyrins: the effect of π-extended conjugation
Elizabeth K. Galván-Miranda, Hiram M. Castro-Cruz, J. Arturo Arias-Orea, Matteo Iurlo, Giovanni Valenti, Massimo Marcaccio, Norma A. Macías-Ruvalcaba
DOI: 10.1039/C6CP01926A
Redox potentials of aryl derivatives from hybrid functional based first principles molecular dynamics
Xiandong Liu, Xiancai Lu, Mengjia He, Rucheng Wang
DOI: 10.1039/C6CP01375A
Thermally stable J-type phthalocyanine dimers as new non-linear absorbers for low-threshold optical limiters
Alexander Yu. Tolbin, Mikhail S. Savelyev, Alexander Yu. Gerasimenko
DOI: 10.1039/C6CP01862A
Final rotational state distributions from NO(vi = 11) in collisions with Au(111): the magnitude of vibrational energy transfer depends on orientation in molecule–surface collisions
Bastian C. Krüger, Nils Bartels, Tim Schäfer
DOI: 10.1039/C6CP02100J
Connectivity matters – ultrafast isomerization dynamics of bisazobenzene photoswitches
Chavdar Slavov, Chong Yang, Luca Schweighauser, Chokri Boumrifak, Andreas Dreuw, Hermann A. Wegner, Josef Wachtveitl
DOI: 10.1039/C6CP00603E
Origin of non-linearity in phase solubility: solubilisation by cyclodextrin beyond stoichiometric complexation
Thomas W. J. Nicol, Seishi Shimizu
DOI: 10.1039/C6CP01582D
I. Dissociation free energies of drug–receptor systems via non-equilibrium alchemical simulations: a theoretical framework
DOI: 10.1039/C5CP05519A
You might also like
Is 4-Benzyl-2,2-dimethylmorpholine (CAS: 84761-04-6) safe?
4-Benzyl-2,2-dimethylmorpholine is generally considered safe when handled under ...
What is (5,6-Dimethoxy-3-pyridinyl)boronic acid (CAS: 1346526-61-1)?
(5,6-Dimethoxy-3-pyridinyl)boronic acid is a chemical compound with the molecula...
How is 1,1,3,3-Tetramethyl-1,3-bis(2-methyl-2-propanyl)disiloxane (CAS: 67875-55-2) typically synthesized?
1,1,3,3-Tetramethyl-1,3-bis(2-methyl-2-propanyl)disiloxane is synthesized throug...
What are the main uses of (2R,4S)-1-Boc-4-methylpyrrolidine-2-carboxylic acid (CAS: 1018818-04-6)?
(2R,4S)-1-Boc-4-methylpyrrolidine-2-carboxylic acid is primarily used as a build...
What precautions should be taken when handling 2,3-Dichloroacrylonitrile (CAS: 22410-58-8)?
When handling 2,3-Dichloroacrylonitrile, it is crucial to wear appropriate perso...
How should (S)-1-(o-Tolyl)ethanamine hydrochloride (CAS: 1332832-16-2) be stored?
(S)-1-(o-Tolyl)ethanamine hydrochloride should be stored in a cool, dry place to...
What are the physical and chemical properties of Benzyl [1-(hydroxyamino)-1-imino-2-methyl-2-propanyl]carbamate (CAS: 518047-98-8)?
Benzyl [1-(hydroxyamino)-1-imino-2-methyl-2-propanyl]carbamate (CAS: 518047-98-8...
What industries use 2-Methyloxazole-5-carbaldehyde (CAS: 885273-42-7)?
2-Methyloxazole-5-carbaldehyde is used in the pharmaceutical industry for the sy...
What is the market or research trend for 2-Methyl-2-propanyl 4-[(1S)-1-hydroxyethyl]-1-piperidinecarboxylate (CAS: 389889-82-1)?
The market for 2-Methyl-2-propanyl 4-[(1S)-1-hydroxyethyl]-1-piperidinecarboxyla...
Is 1-Butyl-3-methylpyridinium bromide (CAS: 26576-85-2) safe?
1-Butyl-3-methylpyridinium bromide is generally considered safe for laboratory u...














![1,4-Piperazinediylbis{[6-(1H-benzimidazol-2-yl)-2-pyridinyl]methanone} structure 1,4-Piperazinediylbis{[6-(1H-benzimidazol-2-yl)-2-pyridinyl]methanone} structure](https://static.chemtradehub.com/structs/191/1912399-75-7-b9f0.webp)
