Aqueous Zn-metal batteries(AZMBs)performance is hampered by freezing water at low temperatures,which hampers their multi-scenario application.Hydrogen bonds(HBs)play a pivotal role in water freezing,and proton transpo...Aqueous Zn-metal batteries(AZMBs)performance is hampered by freezing water at low temperatures,which hampers their multi-scenario application.Hydrogen bonds(HBs)play a pivotal role in water freezing,and proton transport is indispensable for the establishment of HBs.Here,the accelerated proton transport modulates the dynamic hydrogen bonding network of a Zn(BF4)2/EMIMBF4impregnated polyacrylamide/poly(vinyl alcohol)/xanthan gum dual network eutectic gel electrolyte(PPX-ILZSE)for lowtemperature AZMBs.The PPX-ILZSE forms more HBs,shorter HBs lifetimes,higher tetrahedral entropy,and faster desolvation processes,as demonstrated by experimental and theoretical calculations.This enhanced dynamic proton transport promotes rapid cycling of HBs formation-failure,and for polyaniline cathode(PANI)abundant redox sites of proton,confers excellent low temperature electrochemical performance to the Zn//PANI full cell.Specific capacities for 1000 and 5000 cycles at 1 and 5 A g^(-1)were149.8 and 128.4 m A h g^(-1)at room temperature,respectively.Furthermore,specific capacities of 131.1 mA hg^(-1)(92.4%capacity retention)and 0.0066%capacity decay per lap were achieved for 3000and 3500 laps at-30 and 40℃,respectively,at 0.5 A g^(-1).Furthermore,in-situ protective layer of ZnOHF nano-arrays on the Zn anode surface to eliminate dendrite growth and accelerate Zn-ions adsorption and charge transfer.展开更多
Polymeric materials have emerged as a promising alternative to electrolytic solutions in energy storage applications.However,high crystallinity and poor ionic conductivity are the main barriers restricting their daily...Polymeric materials have emerged as a promising alternative to electrolytic solutions in energy storage applications.However,high crystallinity and poor ionic conductivity are the main barriers restricting their daily application.In this study,we propose a polymer electrolyte system consisting of methylcellulose-polyvinyl alcohol(MC-PVA)blend as host material and lithium trifluoromethanesulfonate(LiCF_(3)SO_(3))as dopant,which was prepared using the solution-casting method.The electrochemical impedance spectroscopy(EIS)analysis revealed a maximum conductivity of 5.42×10^(−6) S cm^(−1) with 40 wt.%LiCF_(3)SO_(3).The key findings demonstrated that the variation in the dielectric loss(εi)and dielectric constant(εr)was significantly correlated with the variation in ionic conductivity.Fourier-transform infrared spectroscopy(FTIR)analysis was done to analyse the salt-polymer interaction by observing the shifting of selected bands.By deconvoluting FTIR spectra in the wavenumber range of 970–1100 cm^(−1),transport properties of electrolytes were investigated and found to be improved when the salt concentration was increased to 40 wt.%.Results from the X-ray diffraction(XRD)study suggested that the higher salt concentration promoted the formation of an amorphous phase,which is favourable for ionic conduction.Field emission scanning electron microscopy(FESEM)study demonstrated that the addition of salt altered the surface morphology of MC-PVA.展开更多
This work explores the dielectric and electrochemical properties of solid biopolymer blend electrolytes(SBEs)based on a combination of alginate and polyvinyl alcohol(PVA),doped with varying concentrations of ammonium ...This work explores the dielectric and electrochemical properties of solid biopolymer blend electrolytes(SBEs)based on a combination of alginate and polyvinyl alcohol(PVA),doped with varying concentrations of ammonium iodide(NH4I).The SBEs were synthesized using the solution casting method,and their ac conductivity exhibited an optimal value of 1.01×10^(-5) S·cm^(-1) at 25 wt.%NH4I.Detailed dielectric and modulus spectroscopy analyses revealed distinctive trends in relation to NH4I concentration,suggesting complex dielectric relaxation behavior.The universal power law(UPL)analysis identified the Small Polaron Hopping(SPH)mechanism as the dominant conduction process in the optimal sample.These results demonstrate that NH4I-doped alginate-PVA SBEs possess favorable electrochemical properties,positioning them as potential candidates for energy storage and ionic transport devices.展开更多
Aqueous alkali metal-ion batteries(AAMIBs)have been recognized as emerging electrochemical energy storage technologies for grid-scale applications owning to their intrinsic safety,cost-effectiveness,and environmental ...Aqueous alkali metal-ion batteries(AAMIBs)have been recognized as emerging electrochemical energy storage technologies for grid-scale applications owning to their intrinsic safety,cost-effectiveness,and environmental sustainability.However,the practical application of AAMIBs is still severely constrained by the tendency of aqueous electrolytes to freeze at low temperatures and decompose at high temperatures,limiting their operational temperature range.Considering the urgent need for energy systems with higher adaptability and resilience at various application scenarios,designing novel electrolytes via structure modulation has increasingly emerged as a feasible and economical strategy for the performance optimization of wide-temperature AAMIBs.In this review,the latest advancement of wide-temperature electrolytes for AAMIBs is systematically and comprehensively summarized.Specifically,the key challenges,failure mechanisms,correlations between hydrogen bond behaviors and physicochemical properties,and thermodynamic and kinetic interpretations in aqueous electrolytes are discussed firstly.Additionally,we offer forward-looking insights and innovative design principles for developing aqueous electrolytes capable of operating across a broad temperature range.This review is expected to provide some guidance and reference for the rational design and regulation of widetemperature electrolytes for AAMIBs and promote their future development.展开更多
基金supported by the National Natural Science Foundation of China(NSFC 52432002,52372041,and 52302087)China Postdoctoral Science Foundation(Grant No.2023 M740895)+1 种基金Heilongjiang Touyan Team Programthe Fundamental Research Funds for the Central Universities(Grant No.HIT.OCEF.2021003 and HIT.DZJJ.2025002)。
文摘Aqueous Zn-metal batteries(AZMBs)performance is hampered by freezing water at low temperatures,which hampers their multi-scenario application.Hydrogen bonds(HBs)play a pivotal role in water freezing,and proton transport is indispensable for the establishment of HBs.Here,the accelerated proton transport modulates the dynamic hydrogen bonding network of a Zn(BF4)2/EMIMBF4impregnated polyacrylamide/poly(vinyl alcohol)/xanthan gum dual network eutectic gel electrolyte(PPX-ILZSE)for lowtemperature AZMBs.The PPX-ILZSE forms more HBs,shorter HBs lifetimes,higher tetrahedral entropy,and faster desolvation processes,as demonstrated by experimental and theoretical calculations.This enhanced dynamic proton transport promotes rapid cycling of HBs formation-failure,and for polyaniline cathode(PANI)abundant redox sites of proton,confers excellent low temperature electrochemical performance to the Zn//PANI full cell.Specific capacities for 1000 and 5000 cycles at 1 and 5 A g^(-1)were149.8 and 128.4 m A h g^(-1)at room temperature,respectively.Furthermore,specific capacities of 131.1 mA hg^(-1)(92.4%capacity retention)and 0.0066%capacity decay per lap were achieved for 3000and 3500 laps at-30 and 40℃,respectively,at 0.5 A g^(-1).Furthermore,in-situ protective layer of ZnOHF nano-arrays on the Zn anode surface to eliminate dendrite growth and accelerate Zn-ions adsorption and charge transfer.
基金Universiti Teknologi PETRONAS for the financial support provided through the YUTP-FRG grant(015LC0-631).
文摘Polymeric materials have emerged as a promising alternative to electrolytic solutions in energy storage applications.However,high crystallinity and poor ionic conductivity are the main barriers restricting their daily application.In this study,we propose a polymer electrolyte system consisting of methylcellulose-polyvinyl alcohol(MC-PVA)blend as host material and lithium trifluoromethanesulfonate(LiCF_(3)SO_(3))as dopant,which was prepared using the solution-casting method.The electrochemical impedance spectroscopy(EIS)analysis revealed a maximum conductivity of 5.42×10^(−6) S cm^(−1) with 40 wt.%LiCF_(3)SO_(3).The key findings demonstrated that the variation in the dielectric loss(εi)and dielectric constant(εr)was significantly correlated with the variation in ionic conductivity.Fourier-transform infrared spectroscopy(FTIR)analysis was done to analyse the salt-polymer interaction by observing the shifting of selected bands.By deconvoluting FTIR spectra in the wavenumber range of 970–1100 cm^(−1),transport properties of electrolytes were investigated and found to be improved when the salt concentration was increased to 40 wt.%.Results from the X-ray diffraction(XRD)study suggested that the higher salt concentration promoted the formation of an amorphous phase,which is favourable for ionic conduction.Field emission scanning electron microscopy(FESEM)study demonstrated that the addition of salt altered the surface morphology of MC-PVA.
基金University Malaysia Pahang Al-Sultan Abdullah(UMPSA)under the UMPSA Distinguish Grant(RDU233001)Ministry of Higher Education Malaysia(MOHE)under the FRGS fund(FRGS/1/2023/STG05/UMP/02/2).
文摘This work explores the dielectric and electrochemical properties of solid biopolymer blend electrolytes(SBEs)based on a combination of alginate and polyvinyl alcohol(PVA),doped with varying concentrations of ammonium iodide(NH4I).The SBEs were synthesized using the solution casting method,and their ac conductivity exhibited an optimal value of 1.01×10^(-5) S·cm^(-1) at 25 wt.%NH4I.Detailed dielectric and modulus spectroscopy analyses revealed distinctive trends in relation to NH4I concentration,suggesting complex dielectric relaxation behavior.The universal power law(UPL)analysis identified the Small Polaron Hopping(SPH)mechanism as the dominant conduction process in the optimal sample.These results demonstrate that NH4I-doped alginate-PVA SBEs possess favorable electrochemical properties,positioning them as potential candidates for energy storage and ionic transport devices.
基金supported by the National Natural Science Foundation of China(52002297)National Key R&D Program of China(2022VFB2404800)+1 种基金Wuhan Yellow Crane Talents Program,China Postdoctoral Science Foundation(No.2024M752495)the Postdoctoral Fellowship Program of CPSF(No.GZB20230552).
文摘Aqueous alkali metal-ion batteries(AAMIBs)have been recognized as emerging electrochemical energy storage technologies for grid-scale applications owning to their intrinsic safety,cost-effectiveness,and environmental sustainability.However,the practical application of AAMIBs is still severely constrained by the tendency of aqueous electrolytes to freeze at low temperatures and decompose at high temperatures,limiting their operational temperature range.Considering the urgent need for energy systems with higher adaptability and resilience at various application scenarios,designing novel electrolytes via structure modulation has increasingly emerged as a feasible and economical strategy for the performance optimization of wide-temperature AAMIBs.In this review,the latest advancement of wide-temperature electrolytes for AAMIBs is systematically and comprehensively summarized.Specifically,the key challenges,failure mechanisms,correlations between hydrogen bond behaviors and physicochemical properties,and thermodynamic and kinetic interpretations in aqueous electrolytes are discussed firstly.Additionally,we offer forward-looking insights and innovative design principles for developing aqueous electrolytes capable of operating across a broad temperature range.This review is expected to provide some guidance and reference for the rational design and regulation of widetemperature electrolytes for AAMIBs and promote their future development.
