As a nonmetallic charge carrier,ammonium ion(NH_(4)^(+))has garnered significant attention in the construction of aqueous batteries due to its advantages of low molar mass,small hydration size and rapid diffusion in a...As a nonmetallic charge carrier,ammonium ion(NH_(4)^(+))has garnered significant attention in the construction of aqueous batteries due to its advantages of low molar mass,small hydration size and rapid diffusion in aqueous solutions.Polymers are a kind of potential electro-active materials for aqueous NH_(4)^(+)storage.However,traditional polymer electrodes are typically created by covering the bulky collectors with excessive additives,which could lead to low volume capacity and unsatisfactory stability.Herein,a nanoparticle-like polyimide(PI)was synthesized and then combined with MXene nanosheets to synergistically construct an additive-free and self-standing PI@MXene composite electrode.Significantly,the redox-active PI nanoparticles are enclosed between conductive MXene flakes to create a 3D lamination-like network that promotes electron transmission,while theπ-πinteractions existing between PI and MXene contribute to the enhanced structural integrity and stability within the composite electrode.As such,it delivers superior aqueous NH_(4)^(+)storage behaviors in terms of a notable specific capacity of 110.7 mA·h·cm^(–3) and a long lifespan with only 0.0064%drop each cycle.Furthermore,in-situ Raman and UV–Vis examinations provide evidence of reversible and stable redox mechanism of the PI@MXene composite electrode during NH_(4)^(+)uptake/removal,highlighting its significance in the area of electrochemical energy storage.展开更多
Aqueous rechargeable ammonium-ion batteries(AIBs)have drew considerable attention because of their capacity for high rates,low cost,and high safety.However,developing desired electrodes requiring stable structure in t...Aqueous rechargeable ammonium-ion batteries(AIBs)have drew considerable attention because of their capacity for high rates,low cost,and high safety.However,developing desired electrodes requiring stable structure in the aqueous fast ammoniation/de-ammoniation becomes urgent.Herein,an ammonium ion full battery using Cu_(3)[Fe(CN)_(6)]_(2)(CuHCF)acting to be a cathode and barium vanadate(BVO)acting to be an anode is described.Its excellent electrochemical behavior of Prussian blue analogs and the perfectly matched lattice structure of NH_(4)^(+)is expected.And the open structure of vanadium compounds satisfies the fast ammoniation/de-ammoniation of NH4+is also achieved.As a result of these synergistic effects,the BVO//CuHCF full cell retains 80.5 percent of its capacity following 1000 cycling.These achievements provide new ideas for developing low-cost and long-life AIBs.展开更多
Aqueous ammonium ion batteries are regarded as eco-friendly and sustainable energy storage systems.And applicable host for NH_(4)^(+)in aqueous solution is always in the process of development.On the basis of density ...Aqueous ammonium ion batteries are regarded as eco-friendly and sustainable energy storage systems.And applicable host for NH_(4)^(+)in aqueous solution is always in the process of development.On the basis of density functional theory calcula-tions,the excellent performance of NH_(4)^(+)insertion in Prussian blue analogues(PBAs)is proposed,especially for copper hexacyanoferrate(CuHCF).In this work,we prove the outstanding cycling and rate performance of CuHCF via electrochemical analyses,delivering no capacity fading during ultra-long cycles of 3000 times and high capacity retention of 93.6%at 50 C.One of main contributions to superior performance from highly reversible redox reaction and structural change is verified during the ammoniation/de-ammoniation progresses.More importantly,we propose the NH_(4)^(+)diffusion mechanism in CuHCF based on con-tinuous formation and fracture of hydrogen bonds from a joint theoretical and experimental study,which is another essential reason for rapid charge transfer and superior NH_(4)^(+)storage.Lastly,a full cell by coupling CuHCF cathode and polyaniline anode is constructed to explore the practical application of CuHCF.In brief,the outstanding aqueous NH_(4)^(+)storage in cubic PBAs creates a blueprint for fast and sustainable energy storage.展开更多
Prussian blue and its analogs are extensively investigated as a cathode for ammonium-ion batteries.However,they often suffer from poor electronic conductivity.Here,we report a Ni_(2)Fe(CN)_(6)/multiwalled carbon nanot...Prussian blue and its analogs are extensively investigated as a cathode for ammonium-ion batteries.However,they often suffer from poor electronic conductivity.Here,we report a Ni_(2)Fe(CN)_(6)/multiwalled carbon nanotube composite electrode material,which is prepared using a simple coprecipitation approach.The obtained material consists of nanoparticles with sizes 30-50 nm and the multiwalled carbon nanotube embedded in it.The existence of multiwalled carbon nanotube ensures that the Ni_(2)Fe(CN)_(6)/multiwalled carbon nanotube composite shows excellent electrochemical performance,achieving a discharge capacity of 55.1 mAh·g^(-1)at 1 C and 43.2 mAh·g^(-1)even at 15 C.An increase in the ammoniumion diffusion coefficient and ionic/electron conductivity based on kinetic investigations accounts for their high performance.Furthermore,detailed ex situ characterizations demonstrate that Ni_(2)Fe(CN)_(6)/multiwalled carbon nanotube composite offers three advantages:negligible lattice expansion during cycling,stable structure,and the reversible redox couple.Therefore,the Ni_(2)Fe(CN)_(6)/multiwalled carbon nanotube composite presents a long cycling life and high rate capacity.Finally,our study reports a desirable material for ammonium-ion batteries and provides a practical approach for improving the electrochemical performance of Prussian blue and its analogs.展开更多
基金supported by the National Natural Science Foundation of China(52002157)the Undergraduate Research&Practice Innovation Program of Jiangsu Province(202310289033Z).
文摘As a nonmetallic charge carrier,ammonium ion(NH_(4)^(+))has garnered significant attention in the construction of aqueous batteries due to its advantages of low molar mass,small hydration size and rapid diffusion in aqueous solutions.Polymers are a kind of potential electro-active materials for aqueous NH_(4)^(+)storage.However,traditional polymer electrodes are typically created by covering the bulky collectors with excessive additives,which could lead to low volume capacity and unsatisfactory stability.Herein,a nanoparticle-like polyimide(PI)was synthesized and then combined with MXene nanosheets to synergistically construct an additive-free and self-standing PI@MXene composite electrode.Significantly,the redox-active PI nanoparticles are enclosed between conductive MXene flakes to create a 3D lamination-like network that promotes electron transmission,while theπ-πinteractions existing between PI and MXene contribute to the enhanced structural integrity and stability within the composite electrode.As such,it delivers superior aqueous NH_(4)^(+)storage behaviors in terms of a notable specific capacity of 110.7 mA·h·cm^(–3) and a long lifespan with only 0.0064%drop each cycle.Furthermore,in-situ Raman and UV–Vis examinations provide evidence of reversible and stable redox mechanism of the PI@MXene composite electrode during NH_(4)^(+)uptake/removal,highlighting its significance in the area of electrochemical energy storage.
基金Joint Funds of the National Natural Science Foundation of China(No.U22A20140)the Independent Cultivation Program of Innovation Team of Ji'nan City(No.2019GXRC011)the Natural Science Foundation of Shandong Province,China(No.ZR2021MA073)。
文摘Aqueous rechargeable ammonium-ion batteries(AIBs)have drew considerable attention because of their capacity for high rates,low cost,and high safety.However,developing desired electrodes requiring stable structure in the aqueous fast ammoniation/de-ammoniation becomes urgent.Herein,an ammonium ion full battery using Cu_(3)[Fe(CN)_(6)]_(2)(CuHCF)acting to be a cathode and barium vanadate(BVO)acting to be an anode is described.Its excellent electrochemical behavior of Prussian blue analogs and the perfectly matched lattice structure of NH_(4)^(+)is expected.And the open structure of vanadium compounds satisfies the fast ammoniation/de-ammoniation of NH4+is also achieved.As a result of these synergistic effects,the BVO//CuHCF full cell retains 80.5 percent of its capacity following 1000 cycling.These achievements provide new ideas for developing low-cost and long-life AIBs.
基金This work is sponsored by NSAF joint Fund(U1830106)Science and Technology Innovation 2025 Major Program of Ningbo(2018B10061)National Natural Science Foundation of China(U1632114,51901205),and K.C.Wong Magna Fund in Ningbo University.
文摘Aqueous ammonium ion batteries are regarded as eco-friendly and sustainable energy storage systems.And applicable host for NH_(4)^(+)in aqueous solution is always in the process of development.On the basis of density functional theory calcula-tions,the excellent performance of NH_(4)^(+)insertion in Prussian blue analogues(PBAs)is proposed,especially for copper hexacyanoferrate(CuHCF).In this work,we prove the outstanding cycling and rate performance of CuHCF via electrochemical analyses,delivering no capacity fading during ultra-long cycles of 3000 times and high capacity retention of 93.6%at 50 C.One of main contributions to superior performance from highly reversible redox reaction and structural change is verified during the ammoniation/de-ammoniation progresses.More importantly,we propose the NH_(4)^(+)diffusion mechanism in CuHCF based on con-tinuous formation and fracture of hydrogen bonds from a joint theoretical and experimental study,which is another essential reason for rapid charge transfer and superior NH_(4)^(+)storage.Lastly,a full cell by coupling CuHCF cathode and polyaniline anode is constructed to explore the practical application of CuHCF.In brief,the outstanding aqueous NH_(4)^(+)storage in cubic PBAs creates a blueprint for fast and sustainable energy storage.
基金NSAF joint Fund(Grant No.U1830106)National Natural Science Foundation of China(Grant No.U1632114)+1 种基金Science and Technology Innovation 2025 Major Program of Ningbo(Grant No.2018B10061)K.C.Wong Magna Fund in Ningbo University.
文摘Prussian blue and its analogs are extensively investigated as a cathode for ammonium-ion batteries.However,they often suffer from poor electronic conductivity.Here,we report a Ni_(2)Fe(CN)_(6)/multiwalled carbon nanotube composite electrode material,which is prepared using a simple coprecipitation approach.The obtained material consists of nanoparticles with sizes 30-50 nm and the multiwalled carbon nanotube embedded in it.The existence of multiwalled carbon nanotube ensures that the Ni_(2)Fe(CN)_(6)/multiwalled carbon nanotube composite shows excellent electrochemical performance,achieving a discharge capacity of 55.1 mAh·g^(-1)at 1 C and 43.2 mAh·g^(-1)even at 15 C.An increase in the ammoniumion diffusion coefficient and ionic/electron conductivity based on kinetic investigations accounts for their high performance.Furthermore,detailed ex situ characterizations demonstrate that Ni_(2)Fe(CN)_(6)/multiwalled carbon nanotube composite offers three advantages:negligible lattice expansion during cycling,stable structure,and the reversible redox couple.Therefore,the Ni_(2)Fe(CN)_(6)/multiwalled carbon nanotube composite presents a long cycling life and high rate capacity.Finally,our study reports a desirable material for ammonium-ion batteries and provides a practical approach for improving the electrochemical performance of Prussian blue and its analogs.