The recent emergence of tetragonal phases zirconium dioxide(ZrO_(2))with vacancies has generated significant interest as a highly efficient and stable electrocatalyst with potential applications in trapping polysulfid...The recent emergence of tetragonal phases zirconium dioxide(ZrO_(2))with vacancies has generated significant interest as a highly efficient and stable electrocatalyst with potential applications in trapping polysulfides and facilitating rapid conversion in lithium-sulfur batteries(LSBs).However,the reduction of ZrO_(2)is challenging,even under strong reducing atmospheres at high temperatures and pressures.Consequently,the limited presence of oxygen vacancies results in insufficient active sites and reaction interfaces,thereby hindering practical implementation.Herein,we successfully introduced abundant oxygen vacancies into ZrO_(2)at the nanoscale with the help of carbon nanotubes(CNTs-OH)through hydrogen-etching at lower temperatures and pressures.The introduced oxygen vacancies on ZrO_(2-x)/CNTs-OH can effectively rearrange charge distribution,enhance sulfiphilicity and increase active sites,contributing to high ionic and electronic transfer kinetics,strong binding energy and low redox barriers between polysulfides and ZrO_(2-x).These findings have been experimentally validated and supported by theory calculations.As a result,LSBs assembled with the ZrO_(2-x)/CNTs-OH modified separators demonstrate excellent rate performance,superior cycling stability,and ultra-high sulfur utilization.Especially,at high sulfur loading of 6 mg cm^(-2),the area capacity is still up to 6.3 mA h cm^(-2).This work provides valuable insights into the structural and functional optimization of electrocatalysts for batteries.展开更多
Stable and flexible metal nanoparticles(NPs)with regeneration ability are critical for long-term operation of solid oxide electrolysis cells(SOECs).Herein,a novel perovskite electrode with stoichiometric Pr_(0.4)Sr_(0...Stable and flexible metal nanoparticles(NPs)with regeneration ability are critical for long-term operation of solid oxide electrolysis cells(SOECs).Herein,a novel perovskite electrode with stoichiometric Pr_(0.4)Sr_(0.6)Co_(0.125)Fe_(0.75)Mo_(0.125)O_(3)−δ(PSFCM)is synthesized and studied,which undergoes multiple redox cycles to validate its structural stability and NPs reversibility.The Co-Fe alloy has exsolved from the parent bulk under reducing atmosphere,and is capable of reincorporation into the parent oxide after re-oxidation treatment.During the redox process,we successfully manipulate the size and population density of the exsolved NPs,and find that the average particle size significantly reduces but the population density increases correspondingly.The electrode polarization resistance of the symmetric cell remains stable for 450 h,and even activates after the redox cycling,which may be attributed to the higher quantity and larger specific surface area of the regenerated Co-Fe alloy NPs.Moreover,the electrochemical performance towards carbon dioxide reduction reaction(CO_(2)RR)is evaluated,and the CO_(2)electrolyzer consisting of CoFe@PSCFM-Ce_(0.8)Sm_(0.2)O_(1.9)(SDC)dual-phase electrode exhibits an excellent current density of 1.42 A·cm^(−2)at 1.6 V,which reaches 1.7 times higher than 0.83 A·cm^(−2)for the pristine PSCFM electrode.Overall,with this flexible and reversible high-performance SOEC cathode material,new options and perspectives are provided for the efficient and durable CO_(2)electrolysis.展开更多
Layered P2-type cathodes with high voltage,large capacity,and easy synthesis show great potential for developing sodium(Na)-ion batteries(NIBs).However,the P2–O2 phase transition makes their structural degradation an...Layered P2-type cathodes with high voltage,large capacity,and easy synthesis show great potential for developing sodium(Na)-ion batteries(NIBs).However,the P2–O2 phase transition makes their structural degradation and the Na^(+)/vacancy ordering lowers their redox kinetics.Here,we rationally propose a compositionally graded P2-type cathode,where nickel(Ni)and manganese(Mn)fractions decrease gradually,and cobalt(Co)content increases contiguously from the inside to the outside of a secondary particle.Inside these particles,the Ni/Mn-based compound delivers high capacity and high voltage.On the surface of particles,the Co/Mn-based solid solution offers a stable buffer matrix.Benefiting from these synergistic effects,this graded P2-type cathode shows the elimination of P2–O2 transformation even when charged to 4.4 V,which enables good structural stability,maintaining capacity retention reaching~80%within 300 cycles.Moreover,the Na^(+)/vacancy ordering superstructure is further suppressed,and the Na^(+)diffusion kinetics is significantly improved.The proposed graded structure with optimized chemical composition offers a new perspective for eliminating the unwanted phase transition and thus enhancing the electrochemistry of high-voltage layered cathodes for advanced NIBs.展开更多
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 ...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.展开更多
Metal organic frameworks have been employed as high-performance layered double hydroxide(LDH)composite supercapacitor electrode materials but have shown unsatisfactory redox ability and stability.Herein,a host-guest C...Metal organic frameworks have been employed as high-performance layered double hydroxide(LDH)composite supercapacitor electrode materials but have shown unsatisfactory redox ability and stability.Herein,a host-guest CuMo-based polyoxomet-alate-based metal organic framework(POMOF)with copious electrochemically active sites and strong electrochemical redox activi-ties has been effectively coupled with POM-incorporated CoNi-LDH to develop a nanocomposite(NENU-5@CoNi-LDH)by a simple solvothermal method.The designed electrode shows a high specific capacity of 333.61 mAh·g^(-1) at 1 A·g^(-1).In addition,the novel hy-brid symmetric supercapacitor NENU-5@CoNi-LDH/active carbon(AC)demonstrated a high energy density of 80.8 Wh·kg^(-1) at a power density of 750.7 W·kg^(-1).Interestingly,the nanocomposite of NENU-5@CoNi-LDH exhibits an outstanding capacitance reten-tion of 79%after 5000 charge-discharge cycles at 10 A·g^(-1).This work provides a new strategy and will be the backbone for future energy storage research.展开更多
To address the insulating nature and the shuttle effect of iodide species that would deteriorate the battery performance,herein iron nitride is well-dispersed into porous carbon fibers with good flexibility via the fa...To address the insulating nature and the shuttle effect of iodide species that would deteriorate the battery performance,herein iron nitride is well-dispersed into porous carbon fibers with good flexibility via the facile electrospinning method and subsequent pyrolysis.The polyacrylonitrile precursor introduces the nitrogen doping under thermal treatment while the addition of iron acetylacetonate leads to the insitu formation of iron nitride among the carbon matrix.The crucial pyrolysis procedure is adjustable to determine the hierarchical porous structure and final composition of the novel carbon fiber composites.As the self-supporting electrode for loading iodine,the zinc-iodine battery exhibits a large specific capacity of 214 mAh/g and good cycling stability over 1600 h.In the combination of in-situ/ex-situ experimental measurements with the theoretical analysis,the in-depth understanding of intrinsic interaction between composited support and iodine species elucidates the essential mechanism to promote the redox kinetics of iodine via the anchoring effect and electrocatalytic conversion,thus improving cycling life and rate performance.Such fundamental principles on the basic redox conversion of iodine species would evoke the rational design of advanced iodine-based electrodes for improving battery performance.展开更多
Oxygen redox is considered a new paradigm for increasing the practical capacity and energy density of the layered oxide cathodes for Na-ion batteries. However, severe local structural changes and phase transitions dur...Oxygen redox is considered a new paradigm for increasing the practical capacity and energy density of the layered oxide cathodes for Na-ion batteries. However, severe local structural changes and phase transitions during anionic redox reactions lead to poor electrochemical performance with sluggish kinetics.Here, we propose a synergy of Li-Cu cations in harnessing the full potential of oxygen redox, through Li displacement and suppressed phase transition in P3-type layered oxide cathode. P3-type Na_(0.7)[Li_(0.1)Cu_(0.2)Mn_(0.7)]O_(2) cathode delivers a large specific capacity of ~212 mA h g^(-1)at 15 mA g^(-1). The discharge capacity is maintained up to ~90% of the initial capacity after 100 cycles, with stable occurrence of the oxygen redox in the high-voltage region. Through advanced experimental analyses and first-principles calculations, it is confirmed that a stepwise redox reaction based on Cu and O ions occurs for the charge-compensation mechanism upon charging. Based on a concrete understanding of the reaction mechanism, the Li displacement by the synergy of Li-Cu cations plays a crucial role in suppressing the structural change of the P3-type layered material under the oxygen redox reaction, and it is expected to be an effective strategy for stabilizing the oxygen redox in the layered oxides of Na-ion batteries.展开更多
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 met...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.展开更多
Fiber-shaped batteries that feature outstanding flexibility,light weight,and wovenability are extremely attractive for powering smart wearable electronic textiles,which further stimulates their demand in extreme envir...Fiber-shaped batteries that feature outstanding flexibility,light weight,and wovenability are extremely attractive for powering smart wearable electronic textiles,which further stimulates their demand in extreme environments.However,there are rare reports on ultralow-temperature fiber batteries to date.This is mainly attributed to the poor conductivity of electrodes and freezing of electrolytes that restrain their satisfactory flexible operation in cold environments.Herein,we propose a fiber cooper metal battery consisting of a conductive polyaniline cathode,an anti-freezing Cu(BF4)2+H3PO4electrolyte and an acidresistant copper wire anode,which can withstand various deformations at ultralow temperatures.Impressively,enhanced capacity and cyclic stability can be achieved by cryoactivated abundant reactive sites in the polyaniline,while benefiting from redox reactions with rapid kinetics involving protons rather than copper ions.Consequently,this well-designed polyaniline/Cu fiber battery delivers excellent flexibility without obvious capacity decay after being bent at-30℃,as well as a remarkable discharge capacity of 120.1 mA h g-1and a capacity retention of 96.8%after 2000 cycles at-50℃.The fiber batteries integrated into wearable textiles can power various electronic devices.These performances greatly outperform those of most reported works.Overall,this work provides a promising strategy toward applications of cryogenic wearable energy storage devices.展开更多
Improving the capacitance and energy density is a significant challenge while developing practical and flexible energy storage system(ESS).Redox mediators(RMs),as redox-active electrolyte additives,can provide additio...Improving the capacitance and energy density is a significant challenge while developing practical and flexible energy storage system(ESS).Redox mediators(RMs),as redox-active electrolyte additives,can provide additional energy storing capability via electrochemical faradaic contribution on electrodes for high-performance flexible ESSs.Particularly,determining effective material combinations between electrodes and RMs is essential for maximizing surface faradaic redox reactions for energy-storage performance.In this study,an electrode-RM system comprising heterostructured hybrid(carbon fiber(CF)/MnO_(2)) faradaic electrodes and iodine RMs(I-RMs) in a redox-active electrolyte is investigated.The CF/MnO_(2)with the 1-RMs(CF/MnO_(2)-I) induces dominant catalytic faradaic interaction with the I-RMs,significantly enhancing the surface faradaic kinetics and increasing the overall energy-storage performance.The CF/MnO_(2)-I ESSs show a 12.6-fold(or higher) increased volumetric energy density of 793.81 mWh L^(-1)at a current of 10 μA relative to ESSs using CF/MnO_(2)without I-RMs(CF/MnO_(2)).Moreover,the CF/MnO_(2)-I retains 93.1% of its initial capacitance after 10,000 cycles,validating the excellent cyclability.Finally,the flexibility of the ESSs is tested at different bending angles(180° to 0°),demonstrating its feasibility for flexible and high-wear environments.Therefore,CF/MnO_(2)electrodes present a practical material combination for high-performance flexible energy-storage devices owing to the catalytic faradaic interaction with I-RMs.展开更多
基金the Natural Science Foundation of Shandong Province (ZR2021MB101,ZR2021ME113,ZR2021ME177,and ZR2021QE096)。
文摘The recent emergence of tetragonal phases zirconium dioxide(ZrO_(2))with vacancies has generated significant interest as a highly efficient and stable electrocatalyst with potential applications in trapping polysulfides and facilitating rapid conversion in lithium-sulfur batteries(LSBs).However,the reduction of ZrO_(2)is challenging,even under strong reducing atmospheres at high temperatures and pressures.Consequently,the limited presence of oxygen vacancies results in insufficient active sites and reaction interfaces,thereby hindering practical implementation.Herein,we successfully introduced abundant oxygen vacancies into ZrO_(2)at the nanoscale with the help of carbon nanotubes(CNTs-OH)through hydrogen-etching at lower temperatures and pressures.The introduced oxygen vacancies on ZrO_(2-x)/CNTs-OH can effectively rearrange charge distribution,enhance sulfiphilicity and increase active sites,contributing to high ionic and electronic transfer kinetics,strong binding energy and low redox barriers between polysulfides and ZrO_(2-x).These findings have been experimentally validated and supported by theory calculations.As a result,LSBs assembled with the ZrO_(2-x)/CNTs-OH modified separators demonstrate excellent rate performance,superior cycling stability,and ultra-high sulfur utilization.Especially,at high sulfur loading of 6 mg cm^(-2),the area capacity is still up to 6.3 mA h cm^(-2).This work provides valuable insights into the structural and functional optimization of electrocatalysts for batteries.
基金supported by the National Natural Science Foundation of China(No.U21A20317)the National Key Research and Development Program of China(No.2022YFA1504701)+2 种基金the Fundamental Research Funds for the Central Universities(No.2042022gf0002)the start-up research funds from Wuhan Institute of Technology(No.K202201)Guangdong Basic and Applied Basic Research Foundation(No.2023A1515010429).
文摘Stable and flexible metal nanoparticles(NPs)with regeneration ability are critical for long-term operation of solid oxide electrolysis cells(SOECs).Herein,a novel perovskite electrode with stoichiometric Pr_(0.4)Sr_(0.6)Co_(0.125)Fe_(0.75)Mo_(0.125)O_(3)−δ(PSFCM)is synthesized and studied,which undergoes multiple redox cycles to validate its structural stability and NPs reversibility.The Co-Fe alloy has exsolved from the parent bulk under reducing atmosphere,and is capable of reincorporation into the parent oxide after re-oxidation treatment.During the redox process,we successfully manipulate the size and population density of the exsolved NPs,and find that the average particle size significantly reduces but the population density increases correspondingly.The electrode polarization resistance of the symmetric cell remains stable for 450 h,and even activates after the redox cycling,which may be attributed to the higher quantity and larger specific surface area of the regenerated Co-Fe alloy NPs.Moreover,the electrochemical performance towards carbon dioxide reduction reaction(CO_(2)RR)is evaluated,and the CO_(2)electrolyzer consisting of CoFe@PSCFM-Ce_(0.8)Sm_(0.2)O_(1.9)(SDC)dual-phase electrode exhibits an excellent current density of 1.42 A·cm^(−2)at 1.6 V,which reaches 1.7 times higher than 0.83 A·cm^(−2)for the pristine PSCFM electrode.Overall,with this flexible and reversible high-performance SOEC cathode material,new options and perspectives are provided for the efficient and durable CO_(2)electrolysis.
基金funded by the National Natural Science Foundation of China(No.52102252)the Natural Science Foundation of Shandong Province(No.ZR2021QB052)China Postdoctoral Science Foundation(No.2021T140268).
文摘Layered P2-type cathodes with high voltage,large capacity,and easy synthesis show great potential for developing sodium(Na)-ion batteries(NIBs).However,the P2–O2 phase transition makes their structural degradation and the Na^(+)/vacancy ordering lowers their redox kinetics.Here,we rationally propose a compositionally graded P2-type cathode,where nickel(Ni)and manganese(Mn)fractions decrease gradually,and cobalt(Co)content increases contiguously from the inside to the outside of a secondary particle.Inside these particles,the Ni/Mn-based compound delivers high capacity and high voltage.On the surface of particles,the Co/Mn-based solid solution offers a stable buffer matrix.Benefiting from these synergistic effects,this graded P2-type cathode shows the elimination of P2–O2 transformation even when charged to 4.4 V,which enables good structural stability,maintaining capacity retention reaching~80%within 300 cycles.Moreover,the Na^(+)/vacancy ordering superstructure is further suppressed,and the Na^(+)diffusion kinetics is significantly improved.The proposed graded structure with optimized chemical composition offers a new perspective for eliminating the unwanted phase transition and thus enhancing the electrochemistry of high-voltage layered cathodes for advanced NIBs.
基金supported by the National Natural Science Foundation of China(Grant No.51774216)Hubei Technical Innovation Special Project of China(Grant No.2017ACA185)Science and technology innovation Talent program of Hubei Province(Grant No.2022EJD002).
文摘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.
基金financially supported by the National Natural Science Foundation of China(22001156)the Youth Talent Fund of University Association for Science and Technology in Shaanxi,China(20210602)the Science Foundation of Science and Technology Department of Shaanxi Province(2021JQ-533).
文摘Metal organic frameworks have been employed as high-performance layered double hydroxide(LDH)composite supercapacitor electrode materials but have shown unsatisfactory redox ability and stability.Herein,a host-guest CuMo-based polyoxomet-alate-based metal organic framework(POMOF)with copious electrochemically active sites and strong electrochemical redox activi-ties has been effectively coupled with POM-incorporated CoNi-LDH to develop a nanocomposite(NENU-5@CoNi-LDH)by a simple solvothermal method.The designed electrode shows a high specific capacity of 333.61 mAh·g^(-1) at 1 A·g^(-1).In addition,the novel hy-brid symmetric supercapacitor NENU-5@CoNi-LDH/active carbon(AC)demonstrated a high energy density of 80.8 Wh·kg^(-1) at a power density of 750.7 W·kg^(-1).Interestingly,the nanocomposite of NENU-5@CoNi-LDH exhibits an outstanding capacitance reten-tion of 79%after 5000 charge-discharge cycles at 10 A·g^(-1).This work provides a new strategy and will be the backbone for future energy storage research.
基金financially supported by the National Natural Science Foundation of China(No.22175108)the Natural Scientific Foundation of Shandong Province(Nos.ZR2020JQ09 and ZR2022ZD27)Taishan Scholars Program of Shandong Province,Project for Scientific Research Innovation Team of Young Scholar in Colleges,Universities of Shandong Province(No.2019KJC025).
文摘To address the insulating nature and the shuttle effect of iodide species that would deteriorate the battery performance,herein iron nitride is well-dispersed into porous carbon fibers with good flexibility via the facile electrospinning method and subsequent pyrolysis.The polyacrylonitrile precursor introduces the nitrogen doping under thermal treatment while the addition of iron acetylacetonate leads to the insitu formation of iron nitride among the carbon matrix.The crucial pyrolysis procedure is adjustable to determine the hierarchical porous structure and final composition of the novel carbon fiber composites.As the self-supporting electrode for loading iodine,the zinc-iodine battery exhibits a large specific capacity of 214 mAh/g and good cycling stability over 1600 h.In the combination of in-situ/ex-situ experimental measurements with the theoretical analysis,the in-depth understanding of intrinsic interaction between composited support and iodine species elucidates the essential mechanism to promote the redox kinetics of iodine via the anchoring effect and electrocatalytic conversion,thus improving cycling life and rate performance.Such fundamental principles on the basic redox conversion of iodine species would evoke the rational design of advanced iodine-based electrodes for improving battery performance.
基金supported by the National Research Foundation of Korea grant funded by the Korea government (NRF2021R1A2C1014280)the Fundamental Research Program of the Korea Institute of Material Science (PNK9370)。
文摘Oxygen redox is considered a new paradigm for increasing the practical capacity and energy density of the layered oxide cathodes for Na-ion batteries. However, severe local structural changes and phase transitions during anionic redox reactions lead to poor electrochemical performance with sluggish kinetics.Here, we propose a synergy of Li-Cu cations in harnessing the full potential of oxygen redox, through Li displacement and suppressed phase transition in P3-type layered oxide cathode. P3-type Na_(0.7)[Li_(0.1)Cu_(0.2)Mn_(0.7)]O_(2) cathode delivers a large specific capacity of ~212 mA h g^(-1)at 15 mA g^(-1). The discharge capacity is maintained up to ~90% of the initial capacity after 100 cycles, with stable occurrence of the oxygen redox in the high-voltage region. Through advanced experimental analyses and first-principles calculations, it is confirmed that a stepwise redox reaction based on Cu and O ions occurs for the charge-compensation mechanism upon charging. Based on a concrete understanding of the reaction mechanism, the Li displacement by the synergy of Li-Cu cations plays a crucial role in suppressing the structural change of the P3-type layered material under the oxygen redox reaction, and it is expected to be an effective strategy for stabilizing the oxygen redox in the layered oxides of Na-ion batteries.
基金This work was supported by the National Natural Science Foundation of China(Grant No.51774216)Hubei Technical Innovation Special Project of China(Grant No.2017ACA185)Outstanding Young and Middle-aged Science and Technology Innovation Team Project of Hubei Province(Grant No.T201802).
文摘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.
基金the financial support from the National Natural Science Foundation of China(52273171 and 21875055)the Shenzhen Research Foundation Project(GXWD20201230155427003)。
文摘Fiber-shaped batteries that feature outstanding flexibility,light weight,and wovenability are extremely attractive for powering smart wearable electronic textiles,which further stimulates their demand in extreme environments.However,there are rare reports on ultralow-temperature fiber batteries to date.This is mainly attributed to the poor conductivity of electrodes and freezing of electrolytes that restrain their satisfactory flexible operation in cold environments.Herein,we propose a fiber cooper metal battery consisting of a conductive polyaniline cathode,an anti-freezing Cu(BF4)2+H3PO4electrolyte and an acidresistant copper wire anode,which can withstand various deformations at ultralow temperatures.Impressively,enhanced capacity and cyclic stability can be achieved by cryoactivated abundant reactive sites in the polyaniline,while benefiting from redox reactions with rapid kinetics involving protons rather than copper ions.Consequently,this well-designed polyaniline/Cu fiber battery delivers excellent flexibility without obvious capacity decay after being bent at-30℃,as well as a remarkable discharge capacity of 120.1 mA h g-1and a capacity retention of 96.8%after 2000 cycles at-50℃.The fiber batteries integrated into wearable textiles can power various electronic devices.These performances greatly outperform those of most reported works.Overall,this work provides a promising strategy toward applications of cryogenic wearable energy storage devices.
基金supported by the National Research Foundation of Korea grant funded by the Korean government (MSIT)(2020R1A2C1101039)the Commercializations Promotion Agency for R&D Outcomes (COMPA) grant funded by the Korea government(MSIT)(2021E200)+1 种基金supported by“Regional Innovation Strategy (RIS)” through the National Research Foundation of Korea (NRF) funded by the Ministry of Education(MOE)(2021RIS-004)supported by the Soonchunhyang University Research Fund。
文摘Improving the capacitance and energy density is a significant challenge while developing practical and flexible energy storage system(ESS).Redox mediators(RMs),as redox-active electrolyte additives,can provide additional energy storing capability via electrochemical faradaic contribution on electrodes for high-performance flexible ESSs.Particularly,determining effective material combinations between electrodes and RMs is essential for maximizing surface faradaic redox reactions for energy-storage performance.In this study,an electrode-RM system comprising heterostructured hybrid(carbon fiber(CF)/MnO_(2)) faradaic electrodes and iodine RMs(I-RMs) in a redox-active electrolyte is investigated.The CF/MnO_(2)with the 1-RMs(CF/MnO_(2)-I) induces dominant catalytic faradaic interaction with the I-RMs,significantly enhancing the surface faradaic kinetics and increasing the overall energy-storage performance.The CF/MnO_(2)-I ESSs show a 12.6-fold(or higher) increased volumetric energy density of 793.81 mWh L^(-1)at a current of 10 μA relative to ESSs using CF/MnO_(2)without I-RMs(CF/MnO_(2)).Moreover,the CF/MnO_(2)-I retains 93.1% of its initial capacitance after 10,000 cycles,validating the excellent cyclability.Finally,the flexibility of the ESSs is tested at different bending angles(180° to 0°),demonstrating its feasibility for flexible and high-wear environments.Therefore,CF/MnO_(2)electrodes present a practical material combination for high-performance flexible energy-storage devices owing to the catalytic faradaic interaction with I-RMs.
基金supported by the New Energy Project for Electric Vehicle of National Key Research and Development Program,China(2016YFB0100200)National Natural Science Foundation of China(51671004)~~
