scholarly journals Suppressing vanadium crossover using sulfonated aromatic ion exchange membranes for high performance flow batteries

2020 ◽  
Vol 1 (7) ◽  
pp. 2206-2218
Author(s):  
Tongshuai Wang ◽  
Junyoung Han ◽  
Kihyun Kim ◽  
Andreas Münchinger ◽  
Yuechen Gao ◽  
...  

Novel ion exchange membrane with just the right width of selective aqueous ionic domain (<0.6 nm) and unique functionalities show extraordinary ion selectivity. These unique ion transport properties of our membrane is reflected in a remarkable flow battery performance.

Membranes ◽  
2021 ◽  
Vol 11 (11) ◽  
pp. 867
Author(s):  
Ha-Neul Moon ◽  
Hyeon-Bee Song ◽  
Moon-Sung Kang

In this work, we developed pore-filled ion-exchange membranes (PFIEMs) fabricated for the application to an all-vanadium redox flow battery (VRFB) by filling a hydrocarbon-based ionomer containing a fluorine moiety into the pores of a porous polyethylene (PE) substrate having excellent physical and chemical stabilities. The prepared PFIEMs were shown to possess superior tensile strength (i.e., 136.6 MPa for anion-exchange membrane; 129.9 MPa for cation-exchange membrane) and lower electrical resistance compared with commercial membranes by employing a thin porous PE substrate as a reinforcing material. In addition, by introducing a fluorine moiety into the filling ionomer along with the use of the porous PE substrate, the oxidation stability of the PFIEMs could be greatly improved, and the permeability of vanadium ions could also be significantly reduced. As a result of the evaluation of the charge–discharge performance in the VRFB, it was revealed that the higher the fluorine content in the PFIEMs was, the higher the current efficiency was. Moreover, the voltage efficiency of the PFIEMs was shown to be higher than those of the commercial membranes due to the lower electrical resistance. Consequently, both of the pore-filled anion- and cation-exchange membranes showed superior charge–discharge performances in the VRFB compared with those of hydrocarbon-based commercial membranes.


2016 ◽  
Vol 29 (2) ◽  
pp. 127-132 ◽  
Author(s):  
Ling Zhao ◽  
Fuzhen Li ◽  
Yanqing Guo ◽  
Yilun Dong ◽  
Jinying Liu ◽  
...  

Sulfonated polyether ether ketone (SPEEK)/polyvinylidene fluoride (PVDF) blends are employed to prepare the ion-exchange membranes for vanadium redox flow battery (VRB) application. The addition of the highly crystalline and hydrophobic PVDF effectively confines the swelling behavior of SPEEK. The vanadium ion permeability of SPEEK/PVDF membranes is one order of magnitude lower than that of Nafion117 membrane and SPEEK membrane. In VRB single-cell test, the SPEEK/PVDF binary membranes exhibit higher energy efficiency (EE) than recast SPEEK and Nafion117 at 30 mA cm−2. The blend membrane with 30 wt% of PVDF (S0.7P0.3) shows EE of 83.2% at 30 mA cm−2, which is superior to that of the Nafion117 and recast SPEEK membranes. In the self-discharge test, S0.7P0.3 membrane also possesses twice longer duration in open circuit decay test. These results indicate that the addition of PVDF is a simple and efficient way to improve the ion selectivity of SPEEK. With all the good properties and low cost, the SPEEK/PVDF membranes are expected to have excellent commercial prospects as ion-exchange membranes for VRB system.


2014 ◽  
Vol 7 (9) ◽  
pp. 2986-2998 ◽  
Author(s):  
Shuang Gu ◽  
Ke Gong ◽  
Emily Z. Yan ◽  
Yushan Yan

A redox-flow-battery cell design with multiple ion-exchange membranes is provided to enable combinations of any redox pairs and supporting electrolytes.


2020 ◽  
Vol 22 (14) ◽  
pp. 7283-7293
Author(s):  
Yuanyuan Ji ◽  
Hongxi Luo ◽  
Geoffrey M. Geise

Understanding the effects of polymer chemistry on membrane ion transport properties is critical for enabling efforts to design advanced highly permselective ion exchange membranes for water purification and energy applications.


Membranes ◽  
2021 ◽  
Vol 11 (3) ◽  
pp. 217
Author(s):  
AHM Golam Hyder ◽  
Brian A. Morales ◽  
Malynda A. Cappelle ◽  
Stephen J. Percival ◽  
Leo J. Small ◽  
...  

Electrodialysis (ED) desalination performance of different conventional and laboratory-scale ion exchange membranes (IEMs) has been evaluated by many researchers, but most of these studies used their own sets of experimental parameters such as feed solution compositions and concentrations, superficial velocities of the process streams (diluate, concentrate, and electrode rinse), applied electrical voltages, and types of IEMs. Thus, direct comparison of ED desalination performance of different IEMs is virtually impossible. While the use of different conventional IEMs in ED has been reported, the use of bioinspired ion exchange membrane has not been reported yet. The goal of this study was to evaluate the ED desalination performance differences between novel laboratory‑scale bioinspired IEM and conventional IEMs by determining (i) limiting current density, (ii) current density, (iii) current efficiency, (iv) salinity reduction in diluate stream, (v) normalized specific energy consumption, and (vi) water flux by osmosis as a function of (a) initial concentration of NaCl feed solution (diluate and concentrate streams), (b) superficial velocity of feed solution, and (c) applied stack voltage per cell-pair of membranes. A laboratory‑scale single stage batch-recycle electrodialysis experimental apparatus was assembled with five cell‑pairs of IEMs with an active cross-sectional area of 7.84 cm2. In this study, seven combinations of IEMs (commercial and laboratory-made) were compared: (i) Neosepta AMX/CMX, (ii) PCA PCSA/PCSK, (iii) Fujifilm Type 1 AEM/CEM, (iv) SUEZ AR204SZRA/CR67HMR, (v) Ralex AMH-PES/CMH-PES, (vi) Neosepta AMX/Bare Polycarbonate membrane (Polycarb), and (vii) Neosepta AMX/Sandia novel bioinspired cation exchange membrane (SandiaCEM). ED desalination performance with the Sandia novel bioinspired cation exchange membrane (SandiaCEM) was found to be competitive with commercial Neosepta CMX cation exchange membrane.


2021 ◽  
Vol 12 (1) ◽  
Author(s):  
Jing Hu ◽  
Xiaomin Tang ◽  
Qing Dai ◽  
Zhiqiang Liu ◽  
Huamin Zhang ◽  
...  

AbstractMembranes with fast and selective ions transport are highly demanded for energy storage devices. Layered double hydroxides (LDHs), bearing uniform interlayer galleries and abundant hydroxyl groups covalently bonded within two-dimensional (2D) host layers, make them superb candidates for high-performance membranes. However, related research on LDHs for ions separation is quite rare, especially the deep-going study on ions transport behavior in LDHs. Here, we report a LDHs-based composite membrane with fast and selective ions transport for flow battery application. The hydroxide ions transport through LDHs via vehicular (standard diffusion) & Grotthuss (proton hopping) mechanisms is uncovered. The LDHs-based membrane enables an alkaline zinc-based flow battery to operate at 200 mA cm−2, along with an energy efficiency of 82.36% for 400 cycles. This study offers an in-depth understanding of ions transport in LDHs and further inspires their applications in other energy-related devices.


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