In this study, we report the cost-effective and simple synthesis of carbon-coated α-MnOnanoparticles(α-MnO@C) for use as cathodes of aqueous zinc-ion batteries(ZIBs) for the first time. α-MnO@C was prepared via a g...In this study, we report the cost-effective and simple synthesis of carbon-coated α-MnOnanoparticles(α-MnO@C) for use as cathodes of aqueous zinc-ion batteries(ZIBs) for the first time. α-MnO@C was prepared via a gel formation, using maleic acid(CHO) as the carbon source, followed by annealing at low temperature of 270 °C. A uniform carbon network among the α-MnOnanoparticles was observed by transmission electron microscopy. When tested in a zinc cell, the α-MnO@C exhibited a high initial discharge capacity of 272 m Ah/g under 66 m A/g current density compared to 213 m Ah/g, at the same current density, displayed by the pristine sample. Further, α-MnO@C demonstrated superior cycleability compared to the pristine samples. This study may pave the way for the utilizing carbon-coated MnOelectrodes for aqueous ZIB applications and thereby contribute to realizing high performance eco-friendly batteries.展开更多
Manganese-based material is a prospective cathode material for aqueous zinc ion batteries(ZIBs)by virtue of its high theoretical capacity,high operating voltage,and low price.However,the manganese dissolution during t...Manganese-based material is a prospective cathode material for aqueous zinc ion batteries(ZIBs)by virtue of its high theoretical capacity,high operating voltage,and low price.However,the manganese dissolution during the electrochemical reaction causes its electrochemical cycling stability to be undesirable.In this work,heterointerface engineering-induced oxygen defects are introduced into heterostructure MnO_(2)(δa-MnO_(2))by in situ electrochemical activation to inhibit manganese dissolution for aqueous zinc ion batteries.Meanwhile,the heterointerface between the disordered amorphous and the crystalline MnO_(2)ofδa-MnO_(2)is decisive for the formation of oxygen defects.And the experimental results indicate that the manganese dissolution ofδa-MnO_(2)is considerably inhibited during the charge/discharge cycle.Theoretical analysis indicates that the oxygen defect regulates the electronic and band structure and the Mn-O bonding state of the electrode material,thereby promoting electron transport kinetics as well as inhibiting Mn dissolution.Consequently,the capacity ofδa-MnO_(2)does not degrade after 100 cycles at a current density of 0.5 Ag^(-1)and also 91%capacity retention after 500cycles at 1 Ag^(-1).This study provides a promising insight into the development of high-performance manganese-based cathode materials through a facile and low-cost strategy.展开更多
Graphene/manganese dioxide composites and grapheme/manganese dioxide/sulfur(G/MnO2/S) composite cathode were prepared by hydrothermal method and by vapor permeation, respectively. Their structure, morphology and speci...Graphene/manganese dioxide composites and grapheme/manganese dioxide/sulfur(G/MnO2/S) composite cathode were prepared by hydrothermal method and by vapor permeation, respectively. Their structure, morphology and specific surface area were characterized by X-ray diffraction, electron microanalysis and nitrogen adsorption analysis. The composites show morphology of nanosheets, high specific surface area and even distribution of sulfur. The sulfur accounts for 75% in the G/MnO2/S composite by thermogravimetric analysis. The electrochemical performance of G/S and G/MnO2/S cathode were investigated. The G/MnO2/S composite cathodes show excellent rate performance and cycle stability. At a 0.2C current density, initial discharge specific capacity is 1 061 m A·h·g^-1 and maintains 698 m A·h·g^-1 after 100 cycles;At a 1C current density, maximum discharge capacity reaches 816 m A·h·g^-1 and average capacity decreasing rate is only 0.073%/cycle after running over 400 cycles. Electrochemical mechanism of the composites cathodes was analyzed. The sulfur adsorption of Mn O2 inhibited the loss of active material sulfur, so, the electrochemical performance of the complex was improved.展开更多
为解决MnO_(2)材料在水系锌离子电池(ZIBs)中存在的导电性差、材料利用率低等问题,以农业废弃物椰壳为原料,将低成本、来源丰富、绿色可再生的生物质资源引入到电极材料中,通过高温碳化得到导电性优异的椰壳碳,用水热法在椰壳碳表面生长...为解决MnO_(2)材料在水系锌离子电池(ZIBs)中存在的导电性差、材料利用率低等问题,以农业废弃物椰壳为原料,将低成本、来源丰富、绿色可再生的生物质资源引入到电极材料中,通过高温碳化得到导电性优异的椰壳碳,用水热法在椰壳碳表面生长MnO_(2)纳米粒子,获得椰壳碳@MnO_(2)复合纳米材料。借助扫描电子显微镜(SEM)、X射线衍射仪(XRD)、电化学技术等表征测试手段,分析该复合材料的形貌结构以及电化学性能。结果表明椰壳碳@MnO_(2)在100 mA g^(-1)的电流密度下,经过300次循环,比容量仍高达到344.6 mA h g^(-1),性能远高于商用MnO_(2)材料(64.3 mA h g^(-1));椰壳碳@MnO_(2)优异的导电性,纳米化的结构设计提高了材料利用率,减少了离子扩散路径,带来更快的离子扩散速率,提高了材料的倍率性能,具有良好的应用前景。展开更多
基金supported by the National Research Foundation of Korea(NRF)grant funded by the Korea government(MSIP)(2014R1A2A1A10050821)
文摘In this study, we report the cost-effective and simple synthesis of carbon-coated α-MnOnanoparticles(α-MnO@C) for use as cathodes of aqueous zinc-ion batteries(ZIBs) for the first time. α-MnO@C was prepared via a gel formation, using maleic acid(CHO) as the carbon source, followed by annealing at low temperature of 270 °C. A uniform carbon network among the α-MnOnanoparticles was observed by transmission electron microscopy. When tested in a zinc cell, the α-MnO@C exhibited a high initial discharge capacity of 272 m Ah/g under 66 m A/g current density compared to 213 m Ah/g, at the same current density, displayed by the pristine sample. Further, α-MnO@C demonstrated superior cycleability compared to the pristine samples. This study may pave the way for the utilizing carbon-coated MnOelectrodes for aqueous ZIB applications and thereby contribute to realizing high performance eco-friendly batteries.
基金funds from the National Natural Science Foundation of China(51772082 and 51804106)the Natural Science Foundation of Hunan Province(2023JJ10005)
文摘Manganese-based material is a prospective cathode material for aqueous zinc ion batteries(ZIBs)by virtue of its high theoretical capacity,high operating voltage,and low price.However,the manganese dissolution during the electrochemical reaction causes its electrochemical cycling stability to be undesirable.In this work,heterointerface engineering-induced oxygen defects are introduced into heterostructure MnO_(2)(δa-MnO_(2))by in situ electrochemical activation to inhibit manganese dissolution for aqueous zinc ion batteries.Meanwhile,the heterointerface between the disordered amorphous and the crystalline MnO_(2)ofδa-MnO_(2)is decisive for the formation of oxygen defects.And the experimental results indicate that the manganese dissolution ofδa-MnO_(2)is considerably inhibited during the charge/discharge cycle.Theoretical analysis indicates that the oxygen defect regulates the electronic and band structure and the Mn-O bonding state of the electrode material,thereby promoting electron transport kinetics as well as inhibiting Mn dissolution.Consequently,the capacity ofδa-MnO_(2)does not degrade after 100 cycles at a current density of 0.5 Ag^(-1)and also 91%capacity retention after 500cycles at 1 Ag^(-1).This study provides a promising insight into the development of high-performance manganese-based cathode materials through a facile and low-cost strategy.
基金Supported by the Graduate Freedom Exploration Project Fund of the Central South University(No.502211850).
文摘Graphene/manganese dioxide composites and grapheme/manganese dioxide/sulfur(G/MnO2/S) composite cathode were prepared by hydrothermal method and by vapor permeation, respectively. Their structure, morphology and specific surface area were characterized by X-ray diffraction, electron microanalysis and nitrogen adsorption analysis. The composites show morphology of nanosheets, high specific surface area and even distribution of sulfur. The sulfur accounts for 75% in the G/MnO2/S composite by thermogravimetric analysis. The electrochemical performance of G/S and G/MnO2/S cathode were investigated. The G/MnO2/S composite cathodes show excellent rate performance and cycle stability. At a 0.2C current density, initial discharge specific capacity is 1 061 m A·h·g^-1 and maintains 698 m A·h·g^-1 after 100 cycles;At a 1C current density, maximum discharge capacity reaches 816 m A·h·g^-1 and average capacity decreasing rate is only 0.073%/cycle after running over 400 cycles. Electrochemical mechanism of the composites cathodes was analyzed. The sulfur adsorption of Mn O2 inhibited the loss of active material sulfur, so, the electrochemical performance of the complex was improved.
文摘为解决MnO_(2)材料在水系锌离子电池(ZIBs)中存在的导电性差、材料利用率低等问题,以农业废弃物椰壳为原料,将低成本、来源丰富、绿色可再生的生物质资源引入到电极材料中,通过高温碳化得到导电性优异的椰壳碳,用水热法在椰壳碳表面生长MnO_(2)纳米粒子,获得椰壳碳@MnO_(2)复合纳米材料。借助扫描电子显微镜(SEM)、X射线衍射仪(XRD)、电化学技术等表征测试手段,分析该复合材料的形貌结构以及电化学性能。结果表明椰壳碳@MnO_(2)在100 mA g^(-1)的电流密度下,经过300次循环,比容量仍高达到344.6 mA h g^(-1),性能远高于商用MnO_(2)材料(64.3 mA h g^(-1));椰壳碳@MnO_(2)优异的导电性,纳米化的结构设计提高了材料利用率,减少了离子扩散路径,带来更快的离子扩散速率,提高了材料的倍率性能,具有良好的应用前景。
