Multiple-dimensioned defect engineering for graphite felt electrode of vanadium redox flow battery

The scarcity of wettability,insufficient active sites,and low surface area of graphite felt(GF)have long been suppressing the performance of vanadium redox flow batteries(VRFBs).Herein,an ultra-homogeneous multipledimensioned defect,including nano-scale etching and atomic-scale N,O codoping,was used to modify GF by the molten salt system.NH_(4)Cl and KClO_(3) were added simultaneously to the system to obtain porous N/O co-doped electrode(GF/ON),where KClO_(3) was used to ultra-homogeneously etch,and O-functionalize electrode,and NH4Cl was used as N dopant,respectively.GF/ON presents better electrochemical catalysis for VO_(2)+/VO_(2)+ and V3+/V2+ reactions than only O-functionalized electrodes(GF/O)and GF.The enhanced electrochemical properties are attributed to an increase in active sites,surface area,and wettability,as well as the synergistic effect of N and O,which is also supported by the density functional theory calculations.Further,the cell using GF/ON shows higher discharge capacity,energy efficiency,and stability for cycling performance than the pristine cell at 140 mA cm^(−2) for 200 cycles.Moreover,the energy efficiency of the modified cell is increased by 9.7% from 55.2% for the pristine cell at 260 mA cm^(−2).Such an ultra-homogeneous etching with N and O co-doping through“boiling”molten salt medium provides an effective and practical application potential way to prepare superior electrodes for VRFB.

Nanostructured N-doped carbon materials derived from expandable biomass with superior electrocatalytic performance towards V^(2+)/V^(3+) redox reaction for vanadium redox flow battery

Vanadium redox flow battery(VRFB)is one of the most promising large-scale energy storage systems,which ranges from kilowatt to megawatt.Nevertheless,poor electrochemical activity of electrode for two redox couples still restricts the extensive applications of VRFB.Compared with V^(2+)/V^(3+)redox reaction,V^(2+)/V^(3+)reaction plays a more significant role in voltage loss of VRFB owing to slow heterogeneous electron transfer rate.Herein,N-doped carbon materials derived from scaphium scaphigerum have been developed as negative electrocatalyst by hydrothermal carbonization and high-temperature nitridation treatments.The undoped carbon material hardly has electrocatalytic ability for V^(2+)/V^(3+)reaction.Based on this,N-doped carbon materials with urea as nitrogen source exhibit excellent electrocatalytic properties.And the material nitrided at 850°C(SSC/N-850)exhibits the best performance among those from700 to 1000℃.SSC/N-850 can accelerate the electrode process including V^(2+)/V^(3+)reaction and mass transfer of active ions due to the large reaction place,more active sites,and good hydrophilicity.The effect of catalyst on comprehensive performance of cell was evaluated.SSC/N-850 can improve the charge-discharge performance greatly.Utilization of SSC/N-850 can lessen the electrochemical polarization of cell,further resulting in increased discharge capacity and energy efficiency.Discharge capacity and energy efficiency increase by 81.5%and 9.8%by using SSC/N-850 as negative catalyst at 150 m A cm^(-2),respectively.Our study reveals that the developed biomass-derived carbon materials are the low-cost and efficient negative electrocatalyst for VRFB system.

A new long-side-chain sulfonated poly(2,6-dimethyl-1,4-phenylene oxide)(PPO)/polybenzimidazole(PBI)amphoteric membrane for vanadium redox flow battery

A new amphoteric membrane was prepared by blending long-side-chain sulfonated poly(2,6-dimethyl-1,4-phenylene oxide)(S-L-PPO)and polybenzimidazole(PBI)for vanadium redox flow battery(VRFB)application.An acid-base pair structure formed between the imidazole of PBI and sulfonic acid of S-L-PPO resulted in lowered swelling ratio.It favors to reduce the vanadium permeation.While,the increased sulfonic acid concentration ensured that proton conductivity was still at a high level.As a result,a better balance between the vanadium ion permeation(6.1×10^-9 cm^2·s^-1)and proton conductivity(50.8 m S·cm^-1)in the S-L-PPO/PBI-10%membrane was achieved.The VRFB performance with S-L-PPO/PBI-10%membrane exhibited an EE of 82.7%,which was higher than those of pristine S-L-PPO(81.8%)and Nafion 212(78.0%)at 120 m A·cm^-2.In addition,the S-LPPO/PBI-10%membrane had a much longer self-discharge duration time(142 h)than that of Nafion 212(23 h).

The effect of phosphate additive on the positive electrolyte stability of vanadium redox flow battery

The electrolyte is one of the most important components of vanadium redox flow battery （VRFB）. and its stability and solubility determines the energy density of a VRFB. The performance of current positive elec- trolyte is limited by the low stability of VO2＋ at a higher temperature. Phosphate is proved to be a very effective additive to improve the stability of VO2＋. Even though, the stabilizing mechanism is still not clear, which hinders the further development of VRFBs. In this paper, to clarify the effect of phosphate additive on the positive electrolyte stability, the hydration structures of VO2＋ cations and the reaction mechanisms of precipitation with or without phosphate in the supporting electrolyte of H_2SO_4 solutions were investigated in detail based on calculations of electronic structure. The stable configurations of com- plexes were optimized at the B3LYP/6-311 ＋ G（d,p） level of theory. The zero-point energies and Gibbs free energies for these complexes were further evaluated at the B3LYP/aug-cc-pVTZ level of theory. It shows that a structure of [VO_2（H_2O）_2]＋ surrounded by water molecules in H2S04 solution can be formed at the room temperature. With the temperature rises, [VO_2（H_2O）_2]＋ will lose a proton and form the interme- diate of VO（OH）_3, and the further dehydration among VO（OH）_3 molecules will create the precipitate of V_2O_5. When H_3PO_4 was added into electrolytes, the V-O-P bond-containing neutral compound could be formed through interaction between VO（OH）_3 and H_3PO_4, and the activation energy of forming the V-O-P bond-containing neutral compound is about 7 kcal tool-1 lower than that of the VO（OH）_3 dehydration, which could avoid the precipitation of V_2O_5 and improve the electrolyte stability.

SPES/PVDF Binary Membrane as an Alternative Proton Exchange Membrane in Vanadium Redox Flow Battery Application

SPES/PVDF blends were employed to prepare the ion exchange membranes for vanadium redox flow battery(VRB) application for the first time. The addition of the highly crystalline and hydrophobic PVDF effectively limited the swelling behavior of SPES. The vanadium ion permeability of SPES/PVDF membranes was one order of magnitude lower than that of Nafion 117 membrane and pristine SPES membrane. Single cells with SPES/PVDF composite membranes showed significantly lower capacity loss, higher coulombic efficiency and higher energy efficiency than that with Nafion117 and pristine SPES membranes. The blend membrane with 40 wt% of PVDF(denoted as S_(0.6) P_(0.4)) showed energy efficiency of 83.2% at 30 mA?cm^(-2), which was superior to that of the Nafion117 and SPES membranes. In the self-discharge test, S_(0.6) P_(0.4) membrane showed twice longer duration in open circuit decay than that with Nafion 117 membrane. With all the good properties and low cost, the SPES/PVDF membranes are expected to have excellent commercial prospects as ion exchange membranes for VRB system.

Stability of highly supersaturated vanadium electrolyte solution and characterization of precipitated phases for vanadium redox flow battery

The vanadium redox flow battery(VRFB)has been receiving great attention in recent years as one of the most viable energy storage technologies for large-scale applications.However,higher concentrations of vanadium species are required in the H_(2)O-H_(2)SO_(4) electrolyte in order to improve the VRFB energy density.This might lead to unwanted precipitation of vanadium compounds,whose nature has not been accurately characterized yet.For this purpose,this study reports the preparation ofⅤ^((Ⅱ)),ⅤV^((Ⅲ)),Ⅴ^((Ⅳ))andⅤ^((Ⅴ))supersaturated solutions in a 5 M H_(2)SO_(4)-H_(2)O electrolyte by an electrolytic method,from the only vanadium sulfate compound commercially available(VOSO_(4)).The precipitates obtained by ageing of the stirred solutions are representative of the solids that may form in a VRFB operated with such supersaturated solutions.The solid phases are identified using thermogravimetric analysis,X-ray diffraction and SEM.We report that dissolvedⅤ^((Ⅱ)),Ⅴ^((Ⅲ))andⅤ^((Ⅳ))species precipitate as crystals of VSO_(4),V_(2)(SO_(4))3 and VOSO_(4) hydrates and not in their anhydrous form;conversely V^((Ⅴ))precipitates as an amorphous V_(2) O_(5) oxide partially hydrated.The measured hydration degrees(respectively 1.5,9,3 and 0.26 mol of H_(2)O per mol of compound)might significantly affect the overall engineering of VRFB operating with high vanadium concentrations.

Sucrose pyrolysis assembling carbon nanotubes on graphite felt using for vanadium redox flow battery positive electrode

In the present paper, multi-walled carbon nanotubes（MWCNTs） are successfully assembled on graphite felt（GF） using sucrose pyrolysis method for the first time. The in situ formed pyrolytic carbon is chosen as the binder because it is essentially carbon materials as well as CNTs and GF which has a natural tendency to achieve high bonding strength and low contact resistance. The MWCNTs/GF electrode is demonstrated to increase surface area, reduce polarization, lower charge transfer resistance and improve energy conversion efficiency comparing with GF. This excellent electrochemical performance is mainly ascribed to the high electro-catalytic activity of MWCNTs and increasing surface area.

Insights into the hydrogen evolution reaction in vanadium redox flow batteries:A synchrotron radiation based X-ray imaging study

The parasitic hydrogen evolution reaction(HER)in the negative half-cell of vanadium redox flow batteries(VRFBs)causes severe efficiency losses.Thus,a deeper understanding of this process and the accompanying bubble formation is crucial.This benchmarking study locally analyzes the bubble distribution in thick,porous electrodes for the first time using deep learning-based image segmentation of synchrotron X-ray micro-tomograms.Each large three-dimensional data set was processed precisely in less than one minute while minimizing human errors and pointing out areas of increased HER activity in VRFBs.The study systematically varies the electrode potential and material,concluding that more negative electrode potentials of-200 m V vs.reversible hydrogen electrode(RHE)and lower cause more substantial bubble formation,resulting in bubble fractions of around 15%–20%in carbon felt electrodes.Contrarily,the bubble fractions stay only around 2%in an electrode combining carbon felt and carbon paper.The detected areas with high HER activity,such as the border subregion with more than 30%bubble fraction in carbon felt electrodes,the cutting edges,and preferential spots in the electrode bulk,are potential-independent and suggest that larger electrodes with a higher bulk-to-border ratio might reduce HER-related performance losses.The described combination of electrochemical measurements,local X-ray microtomography,AI-based segmentation,and 3D morphometric analysis is a powerful and novel approach for local bubble analysis in three-dimensional porous electrodes,providing an essential toolkit for a broad community working on bubble-generating electrochemical systems.

Ultrafine SnO_(2)in situ modified graphite felt derived from metal-organic framework as a superior electrode for vanadium redox flow battery

Metal-organic framework(MOF)and its derivatives have low-cost,controllable structure,and good catalytic performance,which are often used in the electrochemical field.In this work,SnO_(2)in situ modified graphite felt(SnO_(2)/GF)is prepared by hydrothermal method then simple thermal treatment using Sn-based MOF(Sn-MOF)as precursor.SnO_(2)is uniformly and firmly distributed on the GF surface rather than the common agglomeration and poor bonding of metal oxides on carbon-based electrodes,providing stable active centers for the VO^(2+)/VO_(2)^(+)and V^(2+)/V^(3+)redox reactions.At250 mA·cm^(-2),the energy efficiency of the battery with SnO_(2)/GF remains at 63.2%,while the blank one has failed.The former battery,at 100 mA·cm^(-2),has higher energy efficiency and good cycle stability(over 200 cycles).The battery performance of this study is better than that of most previous report in metal oxide-related work.This work obtains high-performance composite electrode by simple treatment of MOF,which provides a reference for the application of MOF in vanadium redox flow battery.

Characterization and comparison of organic functional groups effects on electrolyte performance for vanadium redox flow battery

The vanadium redox flow battery with a safe and capacity-controllable large-scale energy storage system offers a new method for the sustainability.In this case,acetic acid,methane sulfonic acid,sulfonic acid,amino methane sulfonic acid,and taurine are used to overcome the low electrolyte energy density and stability limitations,as well as to investigate the effects of various organic functional groups on the vanadium redox flow battery.When compared to the pristine electrolyte(0.22 Ah,5.0 Wh·L^(−1),85.0%),the results show that taurine has the advantage of maintaining vanadium ion concentrations,discharge capacity(1.43 Ah),energy density(33.9 Wh·L^(−1)),and energy efficiency(90.5%)even after several cycles.The acetic acid electrolyte is more conducive to the low-temperature stability of the V(II)electrolyte(177 h at−25℃)than pristine(82 h at−2℃).The−SO_(3)H group,specifically the coaction of the−NH_(2)and−SO_(3)H groups,improves electrolyte stability.The−NH_(2)and−COOH additive groups improved conductivity and electrochemical activity.

Large scale preparation of 20 cm×20 cm graphene modified carbon felt for high performance vanadium redox flow battery

Vanadium redox flow batteries(VRFBs)are widely applied in energy storage systems(e.g.,wind energy,solar energy),while the poor activity of commonly used carbon-based electrode limits their large-scale application.In this study,the graphene modified carbon felt(G/CF)with a large area of 20 cm×20 cm has been successfully prepared by a chemical vapor deposition(CVD)strategy,achieving outstanding electrocatalytic redox reversibility of the VRFBs.The decorating graphene can provide abundant active sites for the vanadium redox reactions.Compared with the pristine carbon felt(CF)electrode,the G/CF composite electrode possesses more defective sites on surface,which enhances activity toward VO^(2+)/VO^(2+)couple and electrochemical performances.For instance,such G/CF electrode delivered remarkable voltage efficiency(VE)of 88.4%and energy efficiency(EE)of 86.4%at 100 mA·cm^(-2),much higher than CF electrode by 2.1%and 3.78%,respectively.The long-term cycling stability of G/CF electrode was further investigated and a high retention value of 47.6%can be achieved over 600 cycles.It is demonstrated that this work develops a promising and effective strategy to synthesize the large size of carbon electrode with high performances for the next-generation VRFBs.

Recent advances in metals and metal oxides as catalysts for vanadium redox flow battery:Properties,structures,and perspectives

Vanadium redox flow battery(VRFB)is a kind of battery with wide application prospect.Electrode material is one of the key components of VRFB,and its stability directly affects the performance of battery.Among all kinds of electrode materials,carbon-based material has the best comprehensive properties.However,carbon-based electrodes still have disadvantages such as poor hydrophilicity and low electrochemical activity which need to be improved.One of the effective ways to improve the performance of electrode is to modify carbon-based material with metals and metal oxides.The metal catalysts have excellent electrical conductivity and high catalytic activity.The metal oxide catalysts have the advantages of low cost,wide variety and strong oxidizing properties.This work introduced the application of metal and metal oxide modified electrodes in VRFB in recent years,classified the catalysts,studied their catalytic performance and mechanism.The metal catalysts were reviewed from precious metals and base metals.The metal oxide catalysts were classified and discussed according to the similar properties of the same group elements.This work compared different modification methods,summarized the research progress of metal and metal oxide modification,and proposes the future development direction of electrodes and catalysts.

Properties of mesoporous carbon modified carbon felt for anode of all-vanadium redox flow battery

A novel anode material for all-vanadium redox flow battery was synthesized by dispersion coating of sol-gel processed(resorcinol-furaldehyde) mesoporous carbon(MPC) onto the surface of polyacrylonitrile carbon felt(CF).The coated samples were then annealed at 900℃ and1100℃ and the subsequent morphology,surface chemistry,and electrochemical properties of the MPC coated CF were characterized and compared with an uncoated CF.Addition of the MPC coating is shown to dramatically increase surface area while also increasing the number of active surface oxygen groups particularly for samples annealed at 1100℃.MPC coating shows a mixed effect on electrochemical properties.Characterization with cyclic voltammetry reveals the introduction of MPC coating provides roughly 30%increase in peak current density for the oxidation and reduction reactions of the V(IV)/V(V) redox couple,which is attributed to the significantly increased number of active reaction sites.However,MPC coating seems to be accompanied by a reduction in conductivity as demonstrated by increased redox peak separation and charge transfer resistance.This negative effect on conductivity can be mitigated by heat treatment(at or above 1100℃) which improves surface graphitization reducing redox peak separation and charge transfer resistance such that it is comparable with uncoated samples.

A review of electrolyte additives and impurities in vanadium redox flow batteries

As one of the most important components of the vanadium redox flow battery （VRFB）, the electrolyte can impose a significant impact on cell properties, performance and capital cost. In particular, the electrolyte composition will influence energy density, operating temperature range and the practical applications of the VRFB. Various approaches to increase the energy density and operating temperature range have been proposed. The presence of electrolyte impurities, or the addition of a small amount of other chemical species into the vanadium solution can alter the stability of the electrolyte and influence cell perfor- mance, operating temperature range, energy density, electrochemical kinetics and cost effectiveness. This review provides a detailed overview of research on electrolyte additives including stabilizing agents, im- mobilizing agents, kinetic enhancers, as well as electrolyte impurities and chemical reductants that can be used for different purposes in the VRFBs.

Facile fabrication of amphoteric semi-interpenetrating network membranes for vanadium flow battery applications

For improvement of vanadium redox flow battery （VRB） performance, novel amphoteric semi- interpenetrating membranes （ASIPN） were prepared using poly（ether ether ketone） （PEEK） and polysul- fone （PSf）, the former bearing sulfonic groups and the latter imidazolium. These two groups form ionic crosslinks between PEEK and PSf; meanwhile, covalent cross links were built between PSf chains with ad- dition of N-（3-aminopropyl）-imidazole. The amphoteric nature of the membrane allows facile proton and anion transport; the IPN structure and the presence of imidazolium cation effectively suppress vanadium ion crossover through the membrane. Therefore, the ASIPN based VRBs show higher Coulombic efficiency and energy efficiency than that assembled with pristine SPEEK and Nation 212 membranes. Our work demonstrates that the ASIPN membranes are promising for VRB applications.

Modified carbon cloth as positive electrode with high electrochemical performance for vanadium redox flow batteries

Carbon cloth modified by hydrothermal treatment in ammonia water is developed as the positive electrode with high electrochemical performance for vanadium redox flow batteries. The SEM shows that the treatment has no obvious influence on the morphology of carbon cloth. XPS measurements indicate that the nitrogenous functional groups can be introduced on the surface of carbon cloth successfully. The electrochemical performance of V(IV)/V(V) redox couple on the prepared electrode is evaluated with cyclic voltammetry and linear sweep voltammetry measurements. The N-doped carbon cloth exhibits outstanding electrochemical activity and reversibility toward V(IV)/V(V) redox couple. The rate constant of V(IV)/V(V) redox reaction on carbon cloth can increase to 2.27 x 10(-4) cm/s from 1.47 x 10(-4) cm/s after nitrogen doping. The cell using N-doped carbon cloth as positive electrode has larger discharge capacity and higher energy efficiency compared with the cell using pristine carbon cloth. The average energy efficiency of the cell using N-doped carbon cloth for 50 cycles at 30 mA/cm(2) is 87.8%, 4.3% larger than that of the cell using pristine carbon cloth. It indicates that the N-doped carbon cloth has a promise application prospect in vanadium redox flow batteries. (C) 2016 Science Press and Dalian Institute of Chemical Physics, Chinese Academy of Sciences. Published by Elsevier B.V. and Science Press. All rights reserved.

Influence of solvent on ion conductivity of polybenzimidazole proton exchange membranes for vanadium redox flow batteries

Polybenzimidazole(PBI)is a kind of proton transport membrane material,and its ion conductivity is a key factor affecting its application in vanadium redox flow batteries(VRFBs).The casting solvent of PBI has a significant influence on the acid doping level of PBI membranes which is closely related to ionic conductivity.In this paper,3,3′-diaminobenzidine(DABz)and 4,4′-Dicarboxydiphenylether(DCDPE)were used as raw materials by solution condensation to prepare the PBI with ether bond groups.The chemical structure of PBI was determined by1H NMR and FT-IR,and the prepared PBI had good solubility which can be dissolved in a variety of solvents.The PBI proton exchange membranes were prepared by solution coating with 5 different solvents of N,N-dimethylformamide(DMF),N,N-dimethylacetamide(DMAc),dimethyl sulfoxide(DMSO),1-methyl-2-pyrrolidone(NMP),methane sulfonic acid(MSA).The effects of different solvents on the ion conductivity and physicochemical properties were discussed in detail.The results showed that the PBI membrane prepared by using MSA as solvent(the PBI+MSA membrane)exhibits high water uptake,acid doping level and low vanadium ion permeability.The VRFB assembled with the PBI+MSA membrane exhibited higher coulombic efficiency(CE)99.87%and voltage efficiency(VE)84.50%than that of the commercial Nafion115 membrane at100 m A·cm-2,and after 480 cycles,the EE value can still be maintained at 83.73%.The self-discharge time of a single battery was recorded to be as long as 1000 h.All experimental data indicated that MSA is the best solvent for casting PBI membrane.

System Energy and Efficiency Analysis of 12.5 W VRFB with Different Flow Rates

Vanadium redox flow battery(VRFB)is considered one of the most potential large-scale energy storage technolo-gies in the future,and its electrolyte flow rate is an important factor affecting the performance of VRFB.To study the effect of electrolyte flow rate on the performance of VRFB,the hydrodynamic model is established and a VRFB system is developed.The results show that under constant current density,with the increase of electrolyte flow rate,not only the coulombic efficiency,energy efficiency,and voltage efficiency will increase,but also the capacity and energy discharged by VRFB will also increase.But on the other hand,as the flow rate increases,the power of the pump also increases,resulting in a decrease in system efficiency.The energy discharged by the system does not increase with the increase in flow rate.Considering the balance between efficiency and pump power loss,it is experimentally proved that 120 mL·min-1 is the optimal working flow rate of the VRFB system,which can maximize the battery performance and discharge more energy.

Boosting catalytic activities of carbon felt electrode towards redox reactions of vanadium ions by defect engineering

Vanadium redox flow batteries(VRFBs)are one of the most promising energy storage systems owing to their safety,efficiency,flexibility and scalability.However,the commercial viability of VRFBs is still hindered by the low electrochemical performance of the available carbon-based electrodes.Defect engineering is a powerful strategy to enhance the redox catalytic activity of carbon-based electrodes for VRFBs.In this paper,uniform carbon defects are introduced on the surfaces of carbon felt(CF)electrode by Ar plasma etching.Together with a higher specific surface area,the Ar plasma treated CF offers additional catalytic sites,allowing faster and more reversible oxidation/reduction reactions of vanadium ions.As a result,the VRFB using plasma treated electrode shows a power density of 1018.3 mW/cm^(2),an energy efficiency(EE)of 84.5%,and the EE remains stable over 1000 cycles.

Optimized the vanadium electrolyte with sulfate-phosphoric mixed acids to enhance the stable operation at high-temperature

Herein, the influence of the concentration design and comprehensive performance of the sulfate-phosphoric mixed acid system electrolyte is investigated to realize an electrolyte that maintains high energy density and stable operation at high temperatures. Static stability tests have shown that VOPO4 precipitation occurs only with vanadium(V) electrolyte. The concentration of vanadium ion of 2.0–2.2 mol·L^(–1), phosphoric acid of 0.10–0.15 mol·L^(–1), and sulfuric acid of 2.5–3.0 mol·L^(–1) are suitable for a vanadium redox flow battery in the temperature range from –20 to 50 ℃. The equations for predicting the viscosity and conductivity of electrolytes are obtained by the response surface method. The optimized electrolyte overcomes precipitation generation. It has 2.8 times higher energy density than the non-phosphate electrolyte, and a coulomb efficiency of 94.0% at 50 ℃. The sulfate-phosphoric mixed acid system electrolyte promotes the electrode reaction process, increases the current density, and reduces the resistance. This work systematically optimizes the concentrations of composition of positive and negative vanadium electrolytes with mixed sulfate-phosphoric acid. It provides a basis for the different valence states and comprehensive properties of sulfate-phosphoric mixed acid system vanadium electrolytes under extreme environments, guiding engineering applications.