采用水热法成功合成了一种新型氮掺杂碳修饰MnO2纳米带(MnO2@NC)。将该材料作为锂离子电池负极时,在2 A g-1的大电流密度下循环1000次后,其可逆比容量可达310.4 mAh g-1,并展现出卓越的倍率并能。与未改性MnO2相比,MnO2@NC表现出更好的...采用水热法成功合成了一种新型氮掺杂碳修饰MnO2纳米带(MnO2@NC)。将该材料作为锂离子电池负极时,在2 A g-1的大电流密度下循环1000次后,其可逆比容量可达310.4 mAh g-1,并展现出卓越的倍率并能。与未改性MnO2相比,MnO2@NC表现出更好的倍率性能、更高的比容量和容量保持率。电化学测试分析表明,MnO2@NC电化学性能提高的原因在于电荷转移电阻的降低、缩短的Li+扩散距离以及更为优异的电极动力学。?展开更多
The commercialization of electrolytic MnO_(2)-Zn batteries is highly applauded owing to the advantages of cost-effectiveness,high safety,high energy density,and durable working performance.However,due to the low rever...The commercialization of electrolytic MnO_(2)-Zn batteries is highly applauded owing to the advantages of cost-effectiveness,high safety,high energy density,and durable working performance.However,due to the low reversibility of the cathode MnO_(2)/Mn^(2+)chemistry at high areal capacities and the severe Zn anode corrosion,the practical application of MnO_(2)-Zn batteries is hampered by inadequate lifespan.Leveraging the full advantage of an iodine redox mediator,here we design a highly rechargeable electrolytic MnO_(2)-Zn battery with a high areal capacity.The MnO_(2)-Zn battery coupled with an iodine mediator in a mild electrolyte shows a high discharge voltage of 1.85 V and a robust areal capacity of 10 mAh cm^(-2)under a substantial discharge current density of 160 mA cm^(-2).The MnO_(2)/I_(2)-Zn battery with an areal capacity of 10 mAh cm^(-2)exhibits prolonged stability of over 950 cycles under a high-capacity retention of~94%.The scaled-up MnO_(2)/I_(2)-Zn battery reveals a stable cycle life under a cell capacity of~600 mAh.Moreover,our constructed MnO_(2)/I_(2)-Zn battery demonstrates a practical energy density of~37 Wh kg^(-1)and a competitive energy cost of<18 US$kWh^(-1)by taking into account the cathode,anode,and electrolyte.The MnO_(2)/I_(2)-Zn battery,with its remarkable reversibility and reasonable energy density,enlightens a new arena of large-scale energy storage devices.展开更多
Aqueous zinc ion batteries(AZIBs) have received great attention because of their non-toxicity,high safety,low cost,high abundance,and high specific power.However,their specific capacity is still low compared with lith...Aqueous zinc ion batteries(AZIBs) have received great attention because of their non-toxicity,high safety,low cost,high abundance,and high specific power.However,their specific capacity is still low compared with lithium ion battery,and current academic research interesting has been focused on developing new cathode materials with high specific capacity.In this study,a Mn/V hybrid polymer framework is designed by a simple self-polymerization scheme.During subsequent calcination,ultrafine VN quantum dots and MnO nanoparticles are generated in situ and stably encapsulated inside N-doped carbon(NC) shells to obtain a novel hybrid cathode NC@VN/MnO for AZIBs.According to the density functional theory(DFT) calculation,the hybrids of MnO and VN can generate both interfacial effects and built-in electric fields that significantly accelerate ion and electron transport by tuning the intrinsic electronic structure,thus enhancing electrochemical performance.A synergistic strategy of composition and structural design allows the rechargeable AZIBs to achieve low-cost and excellent long-cycle performance based on a relay type collaboration at different cycling stages.Consequently,the NC@VN/MnO cathode has output a capacity of 108.3 mA h g^(-1)after 12,000 cycles at 10 A g^(-1).These results clearly and fully demonstrate the advantages of the hybrid cathode NC@VN/MnO.展开更多
Activated carbons calcined at 400˚C and 600˚C (AC-400 and AC-600), prepared using palm nuts, collected in the town of Franceville in Gabon, were used to study the dynamic adsorption of MnO<sub>4</sub>-<...Activated carbons calcined at 400˚C and 600˚C (AC-400 and AC-600), prepared using palm nuts, collected in the town of Franceville in Gabon, were used to study the dynamic adsorption of MnO<sub>4</sub>-</sup> ions in acidic media on fixed bed column and on the kinetic modeling of experimental data of breakthrough curves of MnO<sub>4</sub>-</sup> ions obtained. Results on the adsorption of MnO<sub>4</sub>-</sup> ions in fixed-bed dynamics obtained on AC-400 and AC-600 adsorbents beds indicated that the AC-400 bed appears to be the most efficient in removing MnO<sub>4</sub>-</sup> ions in acidic media. Indeed, the adsorbed amounts, the adsorbed capacities at saturation and the elimination percentage of MnO<sub>4</sub>-</sup> ions obtained with AC-400 (31.24 mg;52.06 mg·g<sup>-1</sup> and 41.65% respectively) were higher compared to those obtained with AC-600 (9.87 mg;16.45 mg·g<sup>-1</sup> and 17.79% respectively). The breakthrough curves kinetic modeling revealed that the Thomas model and the pseudo-first-order kinetic model were the most suitable models to describe the adsorption of MnO<sub>4</sub>-</sup> ions on adsorbents studied in our experimental conditions. The results of the intraparticle diffusion model showed that intraparticle diffusion was involved in the adsorption mechanism of MnO<sub>4</sub>-</sup> ions on investigated adsorbents and was not the limiting step and the only process controlling MnO<sub>4</sub>-</sup> ions adsorption. In contrast to AC-400, the intraparticle diffusion on AC-600 bed plays an important role in the adsorption mechanism of MnO<sub>4</sub>-</sup> ions.展开更多
文摘采用水热法成功合成了一种新型氮掺杂碳修饰MnO2纳米带(MnO2@NC)。将该材料作为锂离子电池负极时,在2 A g-1的大电流密度下循环1000次后,其可逆比容量可达310.4 mAh g-1,并展现出卓越的倍率并能。与未改性MnO2相比,MnO2@NC表现出更好的倍率性能、更高的比容量和容量保持率。电化学测试分析表明,MnO2@NC电化学性能提高的原因在于电荷转移电阻的降低、缩短的Li+扩散距离以及更为优异的电极动力学。?
基金W.C.acknowledges the startup funds from USTC(Grant#KY2060000150)the Fundamental Research Funds for the Central Universities(WK2060000040).
文摘The commercialization of electrolytic MnO_(2)-Zn batteries is highly applauded owing to the advantages of cost-effectiveness,high safety,high energy density,and durable working performance.However,due to the low reversibility of the cathode MnO_(2)/Mn^(2+)chemistry at high areal capacities and the severe Zn anode corrosion,the practical application of MnO_(2)-Zn batteries is hampered by inadequate lifespan.Leveraging the full advantage of an iodine redox mediator,here we design a highly rechargeable electrolytic MnO_(2)-Zn battery with a high areal capacity.The MnO_(2)-Zn battery coupled with an iodine mediator in a mild electrolyte shows a high discharge voltage of 1.85 V and a robust areal capacity of 10 mAh cm^(-2)under a substantial discharge current density of 160 mA cm^(-2).The MnO_(2)/I_(2)-Zn battery with an areal capacity of 10 mAh cm^(-2)exhibits prolonged stability of over 950 cycles under a high-capacity retention of~94%.The scaled-up MnO_(2)/I_(2)-Zn battery reveals a stable cycle life under a cell capacity of~600 mAh.Moreover,our constructed MnO_(2)/I_(2)-Zn battery demonstrates a practical energy density of~37 Wh kg^(-1)and a competitive energy cost of<18 US$kWh^(-1)by taking into account the cathode,anode,and electrolyte.The MnO_(2)/I_(2)-Zn battery,with its remarkable reversibility and reasonable energy density,enlightens a new arena of large-scale energy storage devices.
基金supported by the National Natural Science Foundation of China,China (51772205, 52073212)。
文摘Aqueous zinc ion batteries(AZIBs) have received great attention because of their non-toxicity,high safety,low cost,high abundance,and high specific power.However,their specific capacity is still low compared with lithium ion battery,and current academic research interesting has been focused on developing new cathode materials with high specific capacity.In this study,a Mn/V hybrid polymer framework is designed by a simple self-polymerization scheme.During subsequent calcination,ultrafine VN quantum dots and MnO nanoparticles are generated in situ and stably encapsulated inside N-doped carbon(NC) shells to obtain a novel hybrid cathode NC@VN/MnO for AZIBs.According to the density functional theory(DFT) calculation,the hybrids of MnO and VN can generate both interfacial effects and built-in electric fields that significantly accelerate ion and electron transport by tuning the intrinsic electronic structure,thus enhancing electrochemical performance.A synergistic strategy of composition and structural design allows the rechargeable AZIBs to achieve low-cost and excellent long-cycle performance based on a relay type collaboration at different cycling stages.Consequently,the NC@VN/MnO cathode has output a capacity of 108.3 mA h g^(-1)after 12,000 cycles at 10 A g^(-1).These results clearly and fully demonstrate the advantages of the hybrid cathode NC@VN/MnO.
文摘Activated carbons calcined at 400˚C and 600˚C (AC-400 and AC-600), prepared using palm nuts, collected in the town of Franceville in Gabon, were used to study the dynamic adsorption of MnO<sub>4</sub>-</sup> ions in acidic media on fixed bed column and on the kinetic modeling of experimental data of breakthrough curves of MnO<sub>4</sub>-</sup> ions obtained. Results on the adsorption of MnO<sub>4</sub>-</sup> ions in fixed-bed dynamics obtained on AC-400 and AC-600 adsorbents beds indicated that the AC-400 bed appears to be the most efficient in removing MnO<sub>4</sub>-</sup> ions in acidic media. Indeed, the adsorbed amounts, the adsorbed capacities at saturation and the elimination percentage of MnO<sub>4</sub>-</sup> ions obtained with AC-400 (31.24 mg;52.06 mg·g<sup>-1</sup> and 41.65% respectively) were higher compared to those obtained with AC-600 (9.87 mg;16.45 mg·g<sup>-1</sup> and 17.79% respectively). The breakthrough curves kinetic modeling revealed that the Thomas model and the pseudo-first-order kinetic model were the most suitable models to describe the adsorption of MnO<sub>4</sub>-</sup> ions on adsorbents studied in our experimental conditions. The results of the intraparticle diffusion model showed that intraparticle diffusion was involved in the adsorption mechanism of MnO<sub>4</sub>-</sup> ions on investigated adsorbents and was not the limiting step and the only process controlling MnO<sub>4</sub>-</sup> ions adsorption. In contrast to AC-400, the intraparticle diffusion on AC-600 bed plays an important role in the adsorption mechanism of MnO<sub>4</sub>-</sup> ions.
