钠离子电池因其成本低、资源丰富等优点而成为新一代储能设备.在各种正极中,隧道型Na_(0.44)MnO_(2)因其较大的Na^(+)通道,被认为是快速充电电池的合适正极材料,但仍然存在Na^(+)动力学缓慢等问题.本文首次提出了一种Na_(0.44)MnO_(2)...钠离子电池因其成本低、资源丰富等优点而成为新一代储能设备.在各种正极中,隧道型Na_(0.44)MnO_(2)因其较大的Na^(+)通道,被认为是快速充电电池的合适正极材料,但仍然存在Na^(+)动力学缓慢等问题.本文首次提出了一种Na_(0.44)MnO_(2)的新型离子交换方法,通过调节合成条件,可以很好地控制K^(+)残余量和Na_(0.44)MnO_(2)的尺寸.结果表明,Na_(0.44)MnO_(2)结构中的残留K^(+)扩大了Na^(+)的输运通道,小颗粒形貌缩短了Na^(+)的迁移距离,且晶体中的带状缺陷界面进一步加速了Na^(+)的输运.获得的Na_(0.44)MnO_(2)具有本征赝电容特性,在2-4 V和20 C电流下有79.0 mA h g^(-1)的优异倍率性能.长期循环测试表明,20 C下1000次循环的保持率为98.1%,0.5 C下200次循环的保持率为96.3%.本工作为用于快速充电储能装置的高倍率、高稳定性Na_(0.44)MnO_(2)正极的大规模生产提供了一条新途径.展开更多
Aqueous rechargeable batteries are a possible strategy for large-scale energy storage systems.However,limited choices of anode materials restrict their further application.Here we report phenazine(PNZ)as stable anode ...Aqueous rechargeable batteries are a possible strategy for large-scale energy storage systems.However,limited choices of anode materials restrict their further application.Here we report phenazine(PNZ)as stable anode materials in different alkali-ion(Li+,Na+,K+)electrolyte.A novel full cell is assembled by phenazine anode,Na0.44MnO2 cathode and 10 M NaOH electrolyte to further explore the electrochemical performance of phenazine anode.This battery is able to achieve high capacity(176.7 mAh·g^−1 at 4 C(1.2·Ag^−1)),ultralong cycling life(capacity retention of 80%after 13,000 cycles at 4 C),and excellent rate capacity(92 mAh·g^−1 at 100 C(30 A·g^−1)).The reaction mechanism of PNZ during charge—discharge process is demonstrated by in situ Raman spectroscopy,in situ Fourier transform infrared(FTIR)spectroscopy,X-ray photoelectron spectroscopy(XPS)and density functional theory(DFT)calculations.Furthermore,the system is able to successfully operate at wide temperature range from−20 to 70°C and achieves remarkable electrochemical performance.展开更多
Sodium-ion batteries(SIBs)are promising for grid-scale energy storage applications due to the natural abundance and low cost of sodium.Among various Na insertion cathode materials,Na0.44MnO2 has attracted the most att...Sodium-ion batteries(SIBs)are promising for grid-scale energy storage applications due to the natural abundance and low cost of sodium.Among various Na insertion cathode materials,Na0.44MnO2 has attracted the most attention because of its cost effectiveness and structural stability.However,the low initial charge capacity for Na-poor Na0.44MnO2 hinders its practical applications.Herein,we developed a facile chemical presodiated method using sodiated biphenly to transform Na-poor Na0.44MnO2 into Na-rich Na0.66MnO2.After presodiation,the initial charge capacity of Na0.44MnO2 is greatly enhanced from 56.5 mA·h/g to 115.7 mA·h/g at 0.1 C(1 C=121 mA/g)and the excellent cycling stability(the capacity retention of 94.1%over 200 cycles at 2 C)is achieved.This presodiation strategy would open a new avenue for promoting the practical applications of Na-poor cathode materials in sodium-ion batteries.展开更多
基金supported by the National Natural Science Foundation of China(52202327 and 51972326)the Science and Technology Commission of Shanghai Municipality(22ZR1471300)the Program of Shanghai Academic Research Leader(22XD1424300)。
文摘钠离子电池因其成本低、资源丰富等优点而成为新一代储能设备.在各种正极中,隧道型Na_(0.44)MnO_(2)因其较大的Na^(+)通道,被认为是快速充电电池的合适正极材料,但仍然存在Na^(+)动力学缓慢等问题.本文首次提出了一种Na_(0.44)MnO_(2)的新型离子交换方法,通过调节合成条件,可以很好地控制K^(+)残余量和Na_(0.44)MnO_(2)的尺寸.结果表明,Na_(0.44)MnO_(2)结构中的残留K^(+)扩大了Na^(+)的输运通道,小颗粒形貌缩短了Na^(+)的迁移距离,且晶体中的带状缺陷界面进一步加速了Na^(+)的输运.获得的Na_(0.44)MnO_(2)具有本征赝电容特性,在2-4 V和20 C电流下有79.0 mA h g^(-1)的优异倍率性能.长期循环测试表明,20 C下1000次循环的保持率为98.1%,0.5 C下200次循环的保持率为96.3%.本工作为用于快速充电储能装置的高倍率、高稳定性Na_(0.44)MnO_(2)正极的大规模生产提供了一条新途径.
基金This study was supported by the National Key R&D Program of China(Nos.2016YFB0901500 and 2016YFB0101201)the National Natural Science Foundation of China(No.51771094)+1 种基金Ministry of Education of China(Nos.B12015 and IRT13R30)Tianjin High-Tech(No.18JCZDJC31500).
文摘Aqueous rechargeable batteries are a possible strategy for large-scale energy storage systems.However,limited choices of anode materials restrict their further application.Here we report phenazine(PNZ)as stable anode materials in different alkali-ion(Li+,Na+,K+)electrolyte.A novel full cell is assembled by phenazine anode,Na0.44MnO2 cathode and 10 M NaOH electrolyte to further explore the electrochemical performance of phenazine anode.This battery is able to achieve high capacity(176.7 mAh·g^−1 at 4 C(1.2·Ag^−1)),ultralong cycling life(capacity retention of 80%after 13,000 cycles at 4 C),and excellent rate capacity(92 mAh·g^−1 at 100 C(30 A·g^−1)).The reaction mechanism of PNZ during charge—discharge process is demonstrated by in situ Raman spectroscopy,in situ Fourier transform infrared(FTIR)spectroscopy,X-ray photoelectron spectroscopy(XPS)and density functional theory(DFT)calculations.Furthermore,the system is able to successfully operate at wide temperature range from−20 to 70°C and achieves remarkable electrochemical performance.
基金This work was support by the Regional Innovation and Development Joint Fund,China(No.U20A20249)the National Natural Science Foundation of China(No.21972108)the National Key Research Program of China(No.2016YFB0100200).
文摘Sodium-ion batteries(SIBs)are promising for grid-scale energy storage applications due to the natural abundance and low cost of sodium.Among various Na insertion cathode materials,Na0.44MnO2 has attracted the most attention because of its cost effectiveness and structural stability.However,the low initial charge capacity for Na-poor Na0.44MnO2 hinders its practical applications.Herein,we developed a facile chemical presodiated method using sodiated biphenly to transform Na-poor Na0.44MnO2 into Na-rich Na0.66MnO2.After presodiation,the initial charge capacity of Na0.44MnO2 is greatly enhanced from 56.5 mA·h/g to 115.7 mA·h/g at 0.1 C(1 C=121 mA/g)and the excellent cycling stability(the capacity retention of 94.1%over 200 cycles at 2 C)is achieved.This presodiation strategy would open a new avenue for promoting the practical applications of Na-poor cathode materials in sodium-ion batteries.