The ditheion coefficients(Dapp) and the heterogeneous electron-transfer rate constan(ks)for ferrocene in MPEG/salt electrolytes were determined by using Steady-stae voltammetry. The temperature dependence of the two p...The ditheion coefficients(Dapp) and the heterogeneous electron-transfer rate constan(ks)for ferrocene in MPEG/salt electrolytes were determined by using Steady-stae voltammetry. The temperature dependence of the two parameters obeys the Arrhenius equstion. The effect of the ionic size of sir supporting electrolytes on diffusion and electron transfer dynamics of fermcene was discussed展开更多
The constant increase in global energy demand and stricter environmental standards are calling for advanced energy storage technologies that can store electricity from intermittent renewable sources such as wind,solar...The constant increase in global energy demand and stricter environmental standards are calling for advanced energy storage technologies that can store electricity from intermittent renewable sources such as wind,solar,and tidal power,to allow the broader implementation of the renewables.The gridoriented sodium-ion batteries,potassium ion batteries and multivalent ion batteries are cheaper and more sustainable alternatives to Li-ion,although they are still in the early stages of development.Additional optimisation of these battery systems is required,to improve the energy and power density,and to solve the safety issues caused by dendrites growth in anodes.Electrolyte,one of the most critical components in these batteries,could significantly influence the electrochemical performances and operations of batteries.In this review,the definitions and influences of three critical components(salts,solvents,and additives)in electrolytes are discussed.The significant advantages,challenges,recent progress and future optimisation directions of various electrolytes for monovalent and multivalent ions batteries(i.e.organic,ionic liquid and aqueous liquid electrolytes,polymer and inorganic solid electrolytes)are summarised to guide the practical application for grid-oriented batteries.展开更多
All-solid-state lithium batteries(ASSLBs) employing sulfide electrolyte and lithium(Li) anode have received increasing attention due to the intrinsic safety and high energy density.However,the thick electrolyte layer ...All-solid-state lithium batteries(ASSLBs) employing sulfide electrolyte and lithium(Li) anode have received increasing attention due to the intrinsic safety and high energy density.However,the thick electrolyte layer and lithium dendrites formed at the electrolyte/Li anode interface hinder the realization of high-performance ASSLBs.Herein,a novel membrane consisting of Li_(6)PS_(5) Cl(LPSCl),poly(ethylene oxide)(PEO) and Li-salt(LiTFSI) was prepared as sulfide-based composite solid electrolyte(LPSCl-PEO3-LiTFSI)(LPSCl:PEO=97:3 wt/wt;EO:Li=8:1 mol/mol),which delivers high ionic conductivity(1.1 × 10^(-3) S cm^(-1)) and wide electrochemical window(4.9 V vs.Li^(+)/Li) at 25 ℃.In addition,an ex-situ artificial solid electrolyte interphase(SEI) film enriched with LiF and Li3 N was designed as a protective layer on Li anode(Li(SEI)) to suppress the growth of lithium dendrites.Benefiting from the synergy of sulfide-based composite solid electrolyte and ex-situ artificial SEI,cells of S-CNTs/LPSCI-PEO3-LiTFSI/Li(SEI) and Al_(2)O_(3)@LiNi_(0.5)Co_(0.3)Mn_(0.2)O_(2)/LPSCl-PEO3-LiTFSI/Li(SEI) are assembled and both exhibit high initial discharge capacity of 1221.1 mAh g^(-1)(135.8 mAh g^(-1)) and enhanced cycling stability with 81.6% capacity retention over 200 cycles at 0.05 C(89.2% over 100 cycles at 0.1 C).This work provides a new insight into the synergy of composite solid electrolyte and artificial SEI for achieving high-performance ASSLBs.展开更多
Aluminum(Al) metal has been regarded as a promising anode for rechargeable batteries because of its natural abundance and high theoretical specific capacity. However, rechargeable aluminum batteries(RABs) using A1 met...Aluminum(Al) metal has been regarded as a promising anode for rechargeable batteries because of its natural abundance and high theoretical specific capacity. However, rechargeable aluminum batteries(RABs) using A1 metal as anode display poor cycling performances owing to interface problems between anode and electrolyte. The solid-electrolyte interphase(SEI) layer on the anode has been confirmed to be essential for improving cycling performances of rechargeable batteries. Therefore, we immerse the Al metal in ionic liquid electrolyte for some time before it is used as anode to remove the passive film and expose fresh Al to the electrolyte. Then the reactions of exposed Al, acid, oxygen and water in electrolyte are occurred to form an SEI layer in the cycle. Al/electrolyte/V_2 O_5 full batteries with the thin, uniform and stable SEI layer on Al metal anode perform high discharge capacity and coulombic efficiency(CE). This work illustrates that an SEI layer is formed on Al metal anode in the cycle using a simple and effective pretreatment process and results in superior cycling performances for RABs.展开更多
Rechargeable aluminum batteries(RABs),which use earth-abundant and high-volumetric-capacity metal anodes(8040 m Ah cm-3),have great potential as next-generation power sources because they use cheaper resources to deli...Rechargeable aluminum batteries(RABs),which use earth-abundant and high-volumetric-capacity metal anodes(8040 m Ah cm-3),have great potential as next-generation power sources because they use cheaper resources to deliver higher energies,compared to current lithium ion batteries.However,the mechanism of charge delivery in the newly developed,ionic liquid-based electrolytic system for RABs differs from that in conventional organic electrolytes.Thus,targeted research efforts are required to address the large overpotentials and cycling decay encountered in the ionic liquid-based electrolytic system.In this study,a nanoporous carbon(NPC)electrode with well-developed nanopores is used to develop a high-performance aluminum anode.The negatively charged nanopores can provide quenched dynamics of electrolyte molecules in the aluminum deposition process,resulting in an increased collision rate.The fast chemical equilibrium of anionic species induced by the facilitated anionic collisions leads to more favorable reduction reactions that form aluminum metals.The nanoconfinement effect causes separated nucleation and growth of aluminum nanoparticles in the multiple confined nanopores,leading to higher coulombic efficiencies and more stable cycling performance compared with macroporous carbon black and 2D stainless steel electrodes.展开更多
A new concept of forming solid electrolyte interphases（SEI） in situ in an ionic conducting Li（1.5）Al（0.5）Ge（1.5）（PO4）3-polypropylene（LAGP-PP） based separator during charging and discharging is proposed and...A new concept of forming solid electrolyte interphases（SEI） in situ in an ionic conducting Li（1.5）Al（0.5）Ge（1.5）（PO4）3-polypropylene（LAGP-PP） based separator during charging and discharging is proposed and demonstrated. This unique structure shows a high ionic conductivity, low interface resistance with electrode, and can suppress the growth of lithium dendrite. The features of forming the SEI in situ are investigated by scanning electron microscopy（SEM） and x-ray photoelectron spectroscopy（XPS）. The results confirm that SEI films mainly consist of lithium fluoride and carbonates with various alkyl contents. The cell assembled by using the LAGP-coated separator demonstrates a good cycling performance even at high charging rates, and the lithium dendrites were not observed on the lithium metal electrode. Therefore, the SEI-LAGP-PP separator can be used as a promising flexible solid electrolyte for solid state lithium batteries.展开更多
Dye-sensitized solar cells （DSSCs） are the most promising, low cost and most extensively investigated solar cells. They are famous for their clean and efficient solar energy conversion. Nevertheless this, long-time ...Dye-sensitized solar cells （DSSCs） are the most promising, low cost and most extensively investigated solar cells. They are famous for their clean and efficient solar energy conversion. Nevertheless this, long-time sta- bility is still to be acquired. In recent years research on solid and quasi-solid state electrolytes is extensively in- creased. Various quasi-solid electrolytes, including composites polymer electrolytes, ionic liquid electrolytes, thermoplastic polymer electrolytes and thermosetting polymer electrolytes have been used. Performance and stability of a quasi-solid state electrolyte are between liquid and solid electrolytes. High photovoltaic performances of QS-DSSCs along better long-term stability can be obtained by designing and optimizing quasi-solid electrolytes. It is a prospective candidate for highly efficient and stable DSSCs.展开更多
Effects of nano-ceramic filler titanium oxide（TiO2） have been investigated on the ionic conductance of polymeric complexes consisting of polyvinyl chloride）（PVC）/poly（ethyl methacrylate）（PEMA）,and lithium per...Effects of nano-ceramic filler titanium oxide（TiO2） have been investigated on the ionic conductance of polymeric complexes consisting of polyvinyl chloride）（PVC）/poly（ethyl methacrylate）（PEMA）,and lithium perchlorate（LiClO4）.The composite polymer blend electrolytes were prepared by solvent casting technique.The TiO2 nanofillers were homogeneously dispersed in the polymer electrolyte matrix and exhibited excellent interconnection with PVC/PEMA/PC/UCIO4 polymer electrolyte.The addition of TiO2nanofillers improved the ionic conductivity of the polymer electrolyte to some extent when the content of TiO2 is 15 wt%.The addition of TiO2 also enhanced the thermal stability of the electrolyte.The changes in the structural and complex formation properties of the materials are studied by X-ray diffraction（XRD） and Fourier transform infrared spectroscopy（FTIR） techniques.The scanning electron microscope image of nano-composite polymer electrolyte membrane confirms that the TiO2 nanoparticles were distributed uniformly in the polymer matrix.展开更多
The search for safer next-generation lithium-ion batteries(LIBs)has driven significant research on non-toxic,non-flammable solid electrolytes.However,their electrochemical performance often falls short.This work prese...The search for safer next-generation lithium-ion batteries(LIBs)has driven significant research on non-toxic,non-flammable solid electrolytes.However,their electrochemical performance often falls short.This work presents a simple,one-step photopolymerization process for synthesizing biphasic liquid–solid ionogel electrolytes using acrylic acid monomer and P_(111i4)FSI ionic liquid.We investigated the impact of lithium salt concentration and temperature on ion diffusion,particularly lithium-ion(Li^(+))mobility,within these ionogels.Pulsed-field gradient nuclear magnetic resonance(PFG-NMR)revealed enhanced Li^(+)diffusion in the acrylic acid(AA)-based ionogels compared to their non-confined ionic liquid counterparts.Remarkably,Li^(+)diffusion remained favorable in the ionogels regardless of salt concentration.These AA-based ionogels demonstrate very good ionic conductivity(>1 mS cm^(-1) at room temperature)and a wide electrochemical window(up to 5.3 V vs Li^(+)/Li^(0)).These findings suggest significant promise for AA-based ionogels as polymer solid electrolytes in future solid-state battery applications.展开更多
The wettability of coarse-grained soils has been studied previously.However,soil drying in arid regions due to limited precipitation or irrigation has resulted in soil water repellency to some extent in fine-grained s...The wettability of coarse-grained soils has been studied previously.However,soil drying in arid regions due to limited precipitation or irrigation has resulted in soil water repellency to some extent in fine-grained soils.In this study,laboratory experiments were conducted to investigate the effects of plane(Platanus orientalis L.)leaf biochar with fine(<0.1 mm)and coarse grains(0.1-0.5 mm)on the wettability of a silty clay soil irrigated with saline and non-saline water.Eleven rates of each biochar,ranging from 0 to 10%with 1%intervals,were investigated along with five ionic strengths of water,including 0,0.2,0.4,0.6,and 0.8 mol L^(-1),prepared using sodium and calcium chloride,which are two dominant salts in arid regions.The results showed that application of 5%-10%fine-grained biochar changed the soil hydrophobicity class from strongly to slightly water-repellent,while only 4%coarse-grained biochar was sufficient for the same change in soil wettability.Furthermore,the use of 10%coarse-grained biochar made the soil hydrophilic.The positive effect of plane leaf biochar on soil water repellency reduction was limited by water salinity.The sodium chloride solution was more effective in decreasing the soil wettability than calcium chloride solution and increased the demand for biochar for soil water repellency reduction.In conclusion,plane leaf biochar could be beneficial in managing the hydrophobicity of fine-grained soils.However,water quality as well as biochar particle size determined the quantity of biochar required for improving soil wettability.展开更多
Porous carbon spheres represent an ideal family of electrode materials forsupercapacitors because of the high surface area,ideal conductivity,negligible aggregation,and ability to achieve space efficient packing.Howev...Porous carbon spheres represent an ideal family of electrode materials forsupercapacitors because of the high surface area,ideal conductivity,negligible aggregation,and ability to achieve space efficient packing.However,the development of new synthetic methods towards porous carbon spheres still remains a great challenge.Herein,N-doped hollow carbon spheres with an ultrahigh surface area of2044 m^(2)/g have been designed based on the phenylenediamine-formaldehyde chemistry.When applied in symmetric supercapacitors with ionic electrolyte(EMIBF_4),the obtained N-doped hollow carbon spheres demonstrate a high capacitance of 234 F/g,affording an ultrahigh energy density of 114.8 Wh/kg.Excellent cycling stability has also been achieved.The impressive capacitive performances make the phenylenediamine-formaldehyde resin derived N-doped carbon a promising candidate electrode material for supercapacitors.展开更多
The formation of solid electrolyte interphase(SEI) and ion intercalation are two key processes in rechargeable batteries, which need to be explored under dynamic operating conditions. In this work, both planar and san...The formation of solid electrolyte interphase(SEI) and ion intercalation are two key processes in rechargeable batteries, which need to be explored under dynamic operating conditions. In this work, both planar and sandwich model lithium batteries consisting of Li metal | ionic liquid electrolyte | graphite electrode have been constructed and investigated by a series of in situ surface analysis platforms including atomic force microscopy, Raman and X-ray photoelectron spectroscopy. It is found that the choice of electrolyte, including the concentration and contents, has a profound effect on the SEI formation and evolution, and the subsequent ion intercalation. A smooth and compact SEI is preferably produced in highconcentration electrolytes, with FSI^(-) salt superior to TFSI^(-) salt, facilitating the lithiation/delithiation to achieve high capacity and excellent cycle stability, while suppressing the co-intercalation of electrolyte solvent ions. The innovative research scenario of well-defined model batteries in combination with multiple genuinely in situ surface analysis methods presented herein leads to insightful results, which provide valuable strategies for the rational design and optimization of practical batteries, and energy storage devices in general.展开更多
The solar energy-driven electrochemical CO_(2)reduction to value-added fuels or chemicals is considered as an attractive path to store renewable energy in the form of chemical energy to close the carbon cycle.However,...The solar energy-driven electrochemical CO_(2)reduction to value-added fuels or chemicals is considered as an attractive path to store renewable energy in the form of chemical energy to close the carbon cycle.However,CO_(2)reduction suffers from a number of challenges including slow reaction rates,low selectivity,and low energy conversion efficiency.Recently,innovative strategies have been developed to mitigate this challenges.Especially the development of flow cell reactors with a gas diffusion electrode,ionic liquid electrolytes,and new electrocatalysts have dramatically improved the reaction rates and selectivity to desired products.In this perspective,we highlight the key recent developments and challenges in PVpowered electrochemical CO_(2)reduction and propose effective strategies to improve the reaction kinetics,to minimize the electrical energy losses,and to tune the selectivity of the catalysts for desired products,and then suggest future direction of research and development.展开更多
Ionic gel(IG)electrolytes are emerging as promising components for the development of next-generation supercapacitors(SCs),offering benefits in terms of safety,cost-effectiveness,and flexibility.The ionic conductivity...Ionic gel(IG)electrolytes are emerging as promising components for the development of next-generation supercapacitors(SCs),offering benefits in terms of safety,cost-effectiveness,and flexibility.The ionic conductivity,stability,and mechanical properties of the gel electrolyte are relevant factors to be considered and the key to improving the performance of the SC.However,the structure–activity relationship between the internal structure of IGs and their SC properties is not fully understood.In the current study,the intuitive and regular structure–activity relationship between the structure and properties of IGs was revealed via combining computational simulation and experiment.In terms of conductivity,the ionic liquid(IL)([EMIM][TFSI])in the IG has a high self-diffusion coefficient calculated by molecular dynamics simulation(MDS),which is conductive to transfer and then improves the conductivity.The radial distribution function of the MDS shows that the larger the g(r)between the particles in the polymer network,the stronger the interaction.For stability,IGs based on[EMIM][TFSI]and[EOMIM][TFSI]ILs have higher density functional theory calculated binding energy,which is reflected in the excellent thermal stability and excellent capacitor cycle stability.Based on the internal pore size distribution and stress-strain characterization of the gel network([ME3MePy][TFSI]and[BMIM][TFSI]as additives),the highly crosslinked aggregate network significantly reduces the internal mesoporous distribution and plays a leading role in improving the mechanical properties of the network.By using this strategy,it will be possible to design the ideal structure of the IG and achieve excellent performance.展开更多
Developing electrolyte with high electrochemical stability is the most effective way to improve the energy density of double layer capacitors(DLCs), and ionic liquid is a promising choice. Herein, a novel ionic liquid...Developing electrolyte with high electrochemical stability is the most effective way to improve the energy density of double layer capacitors(DLCs), and ionic liquid is a promising choice. Herein, a novel ionic liquid based high potential electrolyte with a stabilizer, succinonitrile, was proposed to improve the high potential stability of the DLC. The electrolyte with 7.5 wt% succinonitrile added has a high ionic conductivity of 41.1 m S cm^(-1) under ambient temperature, and the DLC adopting this electrolyte could be charged to 3.0 V with stable cycle ability even under a discharge current density of 6 A g^(-1). Moreover, the energy density could be increased by 23.4% when the DLC was charged to 3.0 V compared to that charged to 2.7 V.展开更多
Electric vehicles have been promoted worldwide due to fast-charge technology of ion batteries.However,ion batteries’capacity and cycle life severely decay under extreme conditions,which is mostly related to electroly...Electric vehicles have been promoted worldwide due to fast-charge technology of ion batteries.However,ion batteries’capacity and cycle life severely decay under extreme conditions,which is mostly related to electrolyte conductivity drop and side reactions.This review highlights the safety and stability of ion batteries in terms of thermal stability,non-flammability,low-temperature,and so on,outlining the disadvantages of organic liquid electrolyte,and summarizing effective solutions of polymer electrolytes,solid-state electrolytes,ionic liquid electrolytes,and aqueous electrolytes for the batteries.Moreover,the outlook on the electrolytes is put forward,which is available for research and development of the next generation batteries.展开更多
Increasing the energy density of supercapacitor without sacrificing its high power is an everlasting pursuit in energy storage.Using ionic liquid electrolyte with high operating voltage can increase the energy density...Increasing the energy density of supercapacitor without sacrificing its high power is an everlasting pursuit in energy storage.Using ionic liquid electrolyte with high operating voltage can increase the energy density but usually at the expense of power density due to the large ion size,low ionic conductivity and high viscosity.Herein we demonstrate a simultaneous increase of the energy and power densities with ionic liquid electrolyte(EMIMBF4)mainly by enlarging the ion-transfer micropore channels of the electrode material,i.e.,the unique hierarchical carbon nanocages(hCNC).Boudouard reaction is adopted to tune the micropore size while remaining the hierarchical framework of hCNC.Meanwhile,the specific surface area,pore volume and conductivity are also increased under optimal activation temperature.Such a unique modification boosts the large-sized ion transfer,leading to the obvious decrease of equivalent series resistance and the dramatic increase of supercapacitive performance thereof.The optimized product exhibits an energy density up to 153.8 W h kg^(-1) at the power density of 1.8 kW kg^(-1),and maintains 54.0 W h kg^(-1) even at an ultrahigh power density of 480.1 kW kg^(-1).This study demonstrates an effective way to explore advanced electrode materials by the fine regulation of micropores and related properties.展开更多
Given the increasing attention to the safety issues of lithium-ion batteries(LIBs)and the continuous rise in the price of lithium and its compounds,it is urgent to explore innovative electrochemical energy device alte...Given the increasing attention to the safety issues of lithium-ion batteries(LIBs)and the continuous rise in the price of lithium and its compounds,it is urgent to explore innovative electrochemical energy device alternatives to LIBs.Major efforts have been devoted to developing rechargeable aluminum-ion batteries(AIBs),owing to their low cost and high energy density derived from the 3-electron redox reaction.Moreover,the dendrite-free plating behavior with room-temperature ionic liquid electrolytes endows AIBs with great safety expectations.A marked hurdle persists in the quest for appropriate cathode materials that can effectively accommodate aluminum ion species in AIBs.This review aims to deliver an integrated overview of the state-of-the-art cathode materials for nonaqueous and aqueous AIBs,with a special emphasis on their underlying electrochemical interaction with electrolytes.The strategies adopted to improve the specific capacity and cyclic performances of AIBs are highlighted.Furthermore,future perspectives of AIBs are discussed.展开更多
文摘The ditheion coefficients(Dapp) and the heterogeneous electron-transfer rate constan(ks)for ferrocene in MPEG/salt electrolytes were determined by using Steady-stae voltammetry. The temperature dependence of the two parameters obeys the Arrhenius equstion. The effect of the ionic size of sir supporting electrolytes on diffusion and electron transfer dynamics of fermcene was discussed
文摘The constant increase in global energy demand and stricter environmental standards are calling for advanced energy storage technologies that can store electricity from intermittent renewable sources such as wind,solar,and tidal power,to allow the broader implementation of the renewables.The gridoriented sodium-ion batteries,potassium ion batteries and multivalent ion batteries are cheaper and more sustainable alternatives to Li-ion,although they are still in the early stages of development.Additional optimisation of these battery systems is required,to improve the energy and power density,and to solve the safety issues caused by dendrites growth in anodes.Electrolyte,one of the most critical components in these batteries,could significantly influence the electrochemical performances and operations of batteries.In this review,the definitions and influences of three critical components(salts,solvents,and additives)in electrolytes are discussed.The significant advantages,challenges,recent progress and future optimisation directions of various electrolytes for monovalent and multivalent ions batteries(i.e.organic,ionic liquid and aqueous liquid electrolytes,polymer and inorganic solid electrolytes)are summarised to guide the practical application for grid-oriented batteries.
基金supported by the National Natural Science Foundation of China(51872027)the Fundamental Research Funds for the Central Universities(FRF-TP-20-014A2)。
文摘All-solid-state lithium batteries(ASSLBs) employing sulfide electrolyte and lithium(Li) anode have received increasing attention due to the intrinsic safety and high energy density.However,the thick electrolyte layer and lithium dendrites formed at the electrolyte/Li anode interface hinder the realization of high-performance ASSLBs.Herein,a novel membrane consisting of Li_(6)PS_(5) Cl(LPSCl),poly(ethylene oxide)(PEO) and Li-salt(LiTFSI) was prepared as sulfide-based composite solid electrolyte(LPSCl-PEO3-LiTFSI)(LPSCl:PEO=97:3 wt/wt;EO:Li=8:1 mol/mol),which delivers high ionic conductivity(1.1 × 10^(-3) S cm^(-1)) and wide electrochemical window(4.9 V vs.Li^(+)/Li) at 25 ℃.In addition,an ex-situ artificial solid electrolyte interphase(SEI) film enriched with LiF and Li3 N was designed as a protective layer on Li anode(Li(SEI)) to suppress the growth of lithium dendrites.Benefiting from the synergy of sulfide-based composite solid electrolyte and ex-situ artificial SEI,cells of S-CNTs/LPSCI-PEO3-LiTFSI/Li(SEI) and Al_(2)O_(3)@LiNi_(0.5)Co_(0.3)Mn_(0.2)O_(2)/LPSCl-PEO3-LiTFSI/Li(SEI) are assembled and both exhibit high initial discharge capacity of 1221.1 mAh g^(-1)(135.8 mAh g^(-1)) and enhanced cycling stability with 81.6% capacity retention over 200 cycles at 0.05 C(89.2% over 100 cycles at 0.1 C).This work provides a new insight into the synergy of composite solid electrolyte and artificial SEI for achieving high-performance ASSLBs.
基金supported by the National Basic Research Program of China (No. 2015CB251100)the Program for New Century Excellent Talents in University (NCET-13-0033)+1 种基金the Beijing Co-construction Project (No. 20150939014)the Beijing Higher Institution Engineering Research Center of Power Battery and Chemical Energy Materials
文摘Aluminum(Al) metal has been regarded as a promising anode for rechargeable batteries because of its natural abundance and high theoretical specific capacity. However, rechargeable aluminum batteries(RABs) using A1 metal as anode display poor cycling performances owing to interface problems between anode and electrolyte. The solid-electrolyte interphase(SEI) layer on the anode has been confirmed to be essential for improving cycling performances of rechargeable batteries. Therefore, we immerse the Al metal in ionic liquid electrolyte for some time before it is used as anode to remove the passive film and expose fresh Al to the electrolyte. Then the reactions of exposed Al, acid, oxygen and water in electrolyte are occurred to form an SEI layer in the cycle. Al/electrolyte/V_2 O_5 full batteries with the thin, uniform and stable SEI layer on Al metal anode perform high discharge capacity and coulombic efficiency(CE). This work illustrates that an SEI layer is formed on Al metal anode in the cycle using a simple and effective pretreatment process and results in superior cycling performances for RABs.
基金supported by the Basic Science Research Program through the National Research Foundation of Korea(NRF)Funded by the Ministry of Education(NRF-2019R1A2C1084836,NRF-2018M1A2A2061994,and NRF-2021R1A4A2001403)the KU-KIST School Program。
文摘Rechargeable aluminum batteries(RABs),which use earth-abundant and high-volumetric-capacity metal anodes(8040 m Ah cm-3),have great potential as next-generation power sources because they use cheaper resources to deliver higher energies,compared to current lithium ion batteries.However,the mechanism of charge delivery in the newly developed,ionic liquid-based electrolytic system for RABs differs from that in conventional organic electrolytes.Thus,targeted research efforts are required to address the large overpotentials and cycling decay encountered in the ionic liquid-based electrolytic system.In this study,a nanoporous carbon(NPC)electrode with well-developed nanopores is used to develop a high-performance aluminum anode.The negatively charged nanopores can provide quenched dynamics of electrolyte molecules in the aluminum deposition process,resulting in an increased collision rate.The fast chemical equilibrium of anionic species induced by the facilitated anionic collisions leads to more favorable reduction reactions that form aluminum metals.The nanoconfinement effect causes separated nucleation and growth of aluminum nanoparticles in the multiple confined nanopores,leading to higher coulombic efficiencies and more stable cycling performance compared with macroporous carbon black and 2D stainless steel electrodes.
基金Project supported by the Beijing Science and Technology ProjectChina(Grant No.Z13111000340000)+1 种基金the National Basic Research Program of China(Grant No.2012CB932900)the National Natural Science Foundation of China(Grant Nos.51325206 and 51421002)
文摘A new concept of forming solid electrolyte interphases（SEI） in situ in an ionic conducting Li（1.5）Al（0.5）Ge（1.5）（PO4）3-polypropylene（LAGP-PP） based separator during charging and discharging is proposed and demonstrated. This unique structure shows a high ionic conductivity, low interface resistance with electrode, and can suppress the growth of lithium dendrite. The features of forming the SEI in situ are investigated by scanning electron microscopy（SEM） and x-ray photoelectron spectroscopy（XPS）. The results confirm that SEI films mainly consist of lithium fluoride and carbonates with various alkyl contents. The cell assembled by using the LAGP-coated separator demonstrates a good cycling performance even at high charging rates, and the lithium dendrites were not observed on the lithium metal electrode. Therefore, the SEI-LAGP-PP separator can be used as a promising flexible solid electrolyte for solid state lithium batteries.
文摘Dye-sensitized solar cells （DSSCs） are the most promising, low cost and most extensively investigated solar cells. They are famous for their clean and efficient solar energy conversion. Nevertheless this, long-time sta- bility is still to be acquired. In recent years research on solid and quasi-solid state electrolytes is extensively in- creased. Various quasi-solid electrolytes, including composites polymer electrolytes, ionic liquid electrolytes, thermoplastic polymer electrolytes and thermosetting polymer electrolytes have been used. Performance and stability of a quasi-solid state electrolyte are between liquid and solid electrolytes. High photovoltaic performances of QS-DSSCs along better long-term stability can be obtained by designing and optimizing quasi-solid electrolytes. It is a prospective candidate for highly efficient and stable DSSCs.
基金the UGC,New Delhi,India for providing financial support to carry out this work
文摘Effects of nano-ceramic filler titanium oxide（TiO2） have been investigated on the ionic conductance of polymeric complexes consisting of polyvinyl chloride）（PVC）/poly（ethyl methacrylate）（PEMA）,and lithium perchlorate（LiClO4）.The composite polymer blend electrolytes were prepared by solvent casting technique.The TiO2 nanofillers were homogeneously dispersed in the polymer electrolyte matrix and exhibited excellent interconnection with PVC/PEMA/PC/UCIO4 polymer electrolyte.The addition of TiO2nanofillers improved the ionic conductivity of the polymer electrolyte to some extent when the content of TiO2 is 15 wt%.The addition of TiO2 also enhanced the thermal stability of the electrolyte.The changes in the structural and complex formation properties of the materials are studied by X-ray diffraction（XRD） and Fourier transform infrared spectroscopy（FTIR） techniques.The scanning electron microscope image of nano-composite polymer electrolyte membrane confirms that the TiO2 nanoparticles were distributed uniformly in the polymer matrix.
基金funding from the European Union’s Horizon 2020 research and innovation program under the Marie Skłodowska-Curie Actions COFUND—Grant Agreement No:945357.
文摘The search for safer next-generation lithium-ion batteries(LIBs)has driven significant research on non-toxic,non-flammable solid electrolytes.However,their electrochemical performance often falls short.This work presents a simple,one-step photopolymerization process for synthesizing biphasic liquid–solid ionogel electrolytes using acrylic acid monomer and P_(111i4)FSI ionic liquid.We investigated the impact of lithium salt concentration and temperature on ion diffusion,particularly lithium-ion(Li^(+))mobility,within these ionogels.Pulsed-field gradient nuclear magnetic resonance(PFG-NMR)revealed enhanced Li^(+)diffusion in the acrylic acid(AA)-based ionogels compared to their non-confined ionic liquid counterparts.Remarkably,Li^(+)diffusion remained favorable in the ionogels regardless of salt concentration.These AA-based ionogels demonstrate very good ionic conductivity(>1 mS cm^(-1) at room temperature)and a wide electrochemical window(up to 5.3 V vs Li^(+)/Li^(0)).These findings suggest significant promise for AA-based ionogels as polymer solid electrolytes in future solid-state battery applications.
文摘The wettability of coarse-grained soils has been studied previously.However,soil drying in arid regions due to limited precipitation or irrigation has resulted in soil water repellency to some extent in fine-grained soils.In this study,laboratory experiments were conducted to investigate the effects of plane(Platanus orientalis L.)leaf biochar with fine(<0.1 mm)and coarse grains(0.1-0.5 mm)on the wettability of a silty clay soil irrigated with saline and non-saline water.Eleven rates of each biochar,ranging from 0 to 10%with 1%intervals,were investigated along with five ionic strengths of water,including 0,0.2,0.4,0.6,and 0.8 mol L^(-1),prepared using sodium and calcium chloride,which are two dominant salts in arid regions.The results showed that application of 5%-10%fine-grained biochar changed the soil hydrophobicity class from strongly to slightly water-repellent,while only 4%coarse-grained biochar was sufficient for the same change in soil wettability.Furthermore,the use of 10%coarse-grained biochar made the soil hydrophilic.The positive effect of plane leaf biochar on soil water repellency reduction was limited by water salinity.The sodium chloride solution was more effective in decreasing the soil wettability than calcium chloride solution and increased the demand for biochar for soil water repellency reduction.In conclusion,plane leaf biochar could be beneficial in managing the hydrophobicity of fine-grained soils.However,water quality as well as biochar particle size determined the quantity of biochar required for improving soil wettability.
基金supported by the National Natural Science Foundation of China(Nos.21805219,51521001)the National Key Research and Development Program of China(No.2016YFA0202603)+1 种基金the Program of Introducing Talents of Discipline to Universities(No.B17034)the Yellow Crane Talent(Science&Technology)Program of Wuhan City。
文摘Porous carbon spheres represent an ideal family of electrode materials forsupercapacitors because of the high surface area,ideal conductivity,negligible aggregation,and ability to achieve space efficient packing.However,the development of new synthetic methods towards porous carbon spheres still remains a great challenge.Herein,N-doped hollow carbon spheres with an ultrahigh surface area of2044 m^(2)/g have been designed based on the phenylenediamine-formaldehyde chemistry.When applied in symmetric supercapacitors with ionic electrolyte(EMIBF_4),the obtained N-doped hollow carbon spheres demonstrate a high capacitance of 234 F/g,affording an ultrahigh energy density of 114.8 Wh/kg.Excellent cycling stability has also been achieved.The impressive capacitive performances make the phenylenediamine-formaldehyde resin derived N-doped carbon a promising candidate electrode material for supercapacitors.
基金financially supported by the National Key R&D Program of China(No.2016YFA0200200)the National Natural Science Foundation of China(Nos.21688102 and 21825203)the Strategic Priority Research Program of the Chinese Academy of Sciences(No.XDB17020000)。
文摘The formation of solid electrolyte interphase(SEI) and ion intercalation are two key processes in rechargeable batteries, which need to be explored under dynamic operating conditions. In this work, both planar and sandwich model lithium batteries consisting of Li metal | ionic liquid electrolyte | graphite electrode have been constructed and investigated by a series of in situ surface analysis platforms including atomic force microscopy, Raman and X-ray photoelectron spectroscopy. It is found that the choice of electrolyte, including the concentration and contents, has a profound effect on the SEI formation and evolution, and the subsequent ion intercalation. A smooth and compact SEI is preferably produced in highconcentration electrolytes, with FSI^(-) salt superior to TFSI^(-) salt, facilitating the lithiation/delithiation to achieve high capacity and excellent cycle stability, while suppressing the co-intercalation of electrolyte solvent ions. The innovative research scenario of well-defined model batteries in combination with multiple genuinely in situ surface analysis methods presented herein leads to insightful results, which provide valuable strategies for the rational design and optimization of practical batteries, and energy storage devices in general.
基金supported by the Climate Change Response Project(NRF-2019M1A2A2065612)the Basic Science Grant(NRF2019R1A4A1029237)+2 种基金the Korea-China Key Joint Research Program(2017K2A9A2A11070341)funded by the Ministry of Science and ICT,and by the 2019 Research Fund(1.190013.01)of UNISTsupport from‘‘Carbon to X Project”(Project No.2020M3H7A1098231)through the National Research Foundation(NRF)funded by the Ministry of Science and ICT,Republic of Korea。
文摘The solar energy-driven electrochemical CO_(2)reduction to value-added fuels or chemicals is considered as an attractive path to store renewable energy in the form of chemical energy to close the carbon cycle.However,CO_(2)reduction suffers from a number of challenges including slow reaction rates,low selectivity,and low energy conversion efficiency.Recently,innovative strategies have been developed to mitigate this challenges.Especially the development of flow cell reactors with a gas diffusion electrode,ionic liquid electrolytes,and new electrocatalysts have dramatically improved the reaction rates and selectivity to desired products.In this perspective,we highlight the key recent developments and challenges in PVpowered electrochemical CO_(2)reduction and propose effective strategies to improve the reaction kinetics,to minimize the electrical energy losses,and to tune the selectivity of the catalysts for desired products,and then suggest future direction of research and development.
基金This study was supported by the National Natural Science Foundation of China(22222502)The authors would like to thank the Key Project of the Education Department of Liaoning Province of China(No.LJKZ1010)+1 种基金the Zhenjiang“Jinshan Talents”Project 2021,the Doctoral Foundation of Bohai University(0521bs005)the Innovation Fund Project for Graduate Students of Bohai University(YJC2023-016).
文摘Ionic gel(IG)electrolytes are emerging as promising components for the development of next-generation supercapacitors(SCs),offering benefits in terms of safety,cost-effectiveness,and flexibility.The ionic conductivity,stability,and mechanical properties of the gel electrolyte are relevant factors to be considered and the key to improving the performance of the SC.However,the structure–activity relationship between the internal structure of IGs and their SC properties is not fully understood.In the current study,the intuitive and regular structure–activity relationship between the structure and properties of IGs was revealed via combining computational simulation and experiment.In terms of conductivity,the ionic liquid(IL)([EMIM][TFSI])in the IG has a high self-diffusion coefficient calculated by molecular dynamics simulation(MDS),which is conductive to transfer and then improves the conductivity.The radial distribution function of the MDS shows that the larger the g(r)between the particles in the polymer network,the stronger the interaction.For stability,IGs based on[EMIM][TFSI]and[EOMIM][TFSI]ILs have higher density functional theory calculated binding energy,which is reflected in the excellent thermal stability and excellent capacitor cycle stability.Based on the internal pore size distribution and stress-strain characterization of the gel network([ME3MePy][TFSI]and[BMIM][TFSI]as additives),the highly crosslinked aggregate network significantly reduces the internal mesoporous distribution and plays a leading role in improving the mechanical properties of the network.By using this strategy,it will be possible to design the ideal structure of the IG and achieve excellent performance.
基金supported by the International S&T Cooperation Program of China (2014DFA61670)the Key Program of National Natural Science Foundation of China (91434203)+1 种基金the International Cooperation and Exchange of the National Natural Science Foundation of China (51561145020)the Strategic Priority Research Program of the Chinese Academy of Sciences (XDA09010103)
文摘Developing electrolyte with high electrochemical stability is the most effective way to improve the energy density of double layer capacitors(DLCs), and ionic liquid is a promising choice. Herein, a novel ionic liquid based high potential electrolyte with a stabilizer, succinonitrile, was proposed to improve the high potential stability of the DLC. The electrolyte with 7.5 wt% succinonitrile added has a high ionic conductivity of 41.1 m S cm^(-1) under ambient temperature, and the DLC adopting this electrolyte could be charged to 3.0 V with stable cycle ability even under a discharge current density of 6 A g^(-1). Moreover, the energy density could be increased by 23.4% when the DLC was charged to 3.0 V compared to that charged to 2.7 V.
基金supported by National Natural Science Foundation of China(No.21706013)the State Key Laboratory of Automotive Safety and Energy(No.KFY2217).
文摘Electric vehicles have been promoted worldwide due to fast-charge technology of ion batteries.However,ion batteries’capacity and cycle life severely decay under extreme conditions,which is mostly related to electrolyte conductivity drop and side reactions.This review highlights the safety and stability of ion batteries in terms of thermal stability,non-flammability,low-temperature,and so on,outlining the disadvantages of organic liquid electrolyte,and summarizing effective solutions of polymer electrolytes,solid-state electrolytes,ionic liquid electrolytes,and aqueous electrolytes for the batteries.Moreover,the outlook on the electrolytes is put forward,which is available for research and development of the next generation batteries.
基金supported by the National Key Research and Development Program of China (2017YFA0206500and 2018YFA0209103)the National Natural Science Foundation of China (21832003, 21773111, 21573107 and 21971061)the Fundamental Research Funds for the Central Universities (020514380126)
文摘Increasing the energy density of supercapacitor without sacrificing its high power is an everlasting pursuit in energy storage.Using ionic liquid electrolyte with high operating voltage can increase the energy density but usually at the expense of power density due to the large ion size,low ionic conductivity and high viscosity.Herein we demonstrate a simultaneous increase of the energy and power densities with ionic liquid electrolyte(EMIMBF4)mainly by enlarging the ion-transfer micropore channels of the electrode material,i.e.,the unique hierarchical carbon nanocages(hCNC).Boudouard reaction is adopted to tune the micropore size while remaining the hierarchical framework of hCNC.Meanwhile,the specific surface area,pore volume and conductivity are also increased under optimal activation temperature.Such a unique modification boosts the large-sized ion transfer,leading to the obvious decrease of equivalent series resistance and the dramatic increase of supercapacitive performance thereof.The optimized product exhibits an energy density up to 153.8 W h kg^(-1) at the power density of 1.8 kW kg^(-1),and maintains 54.0 W h kg^(-1) even at an ultrahigh power density of 480.1 kW kg^(-1).This study demonstrates an effective way to explore advanced electrode materials by the fine regulation of micropores and related properties.
基金supported by the BRICS STI Framework Programme(No.52261145703)the National 111 Project(No.B16016).
文摘Given the increasing attention to the safety issues of lithium-ion batteries(LIBs)and the continuous rise in the price of lithium and its compounds,it is urgent to explore innovative electrochemical energy device alternatives to LIBs.Major efforts have been devoted to developing rechargeable aluminum-ion batteries(AIBs),owing to their low cost and high energy density derived from the 3-electron redox reaction.Moreover,the dendrite-free plating behavior with room-temperature ionic liquid electrolytes endows AIBs with great safety expectations.A marked hurdle persists in the quest for appropriate cathode materials that can effectively accommodate aluminum ion species in AIBs.This review aims to deliver an integrated overview of the state-of-the-art cathode materials for nonaqueous and aqueous AIBs,with a special emphasis on their underlying electrochemical interaction with electrolytes.The strategies adopted to improve the specific capacity and cyclic performances of AIBs are highlighted.Furthermore,future perspectives of AIBs are discussed.
