针对AZ31镁合金作为镁电池负极时存在自腐蚀速率大、阳极极化、电位滞后等问题,寻找合适的缓蚀剂及其用量调配电解液以提高电池的放电性能。通过腐蚀浸泡试验表征了缓蚀剂Li_(2)CrO_(4)的缓蚀效果,然后通过极化曲线、电化学阻抗谱研究了...针对AZ31镁合金作为镁电池负极时存在自腐蚀速率大、阳极极化、电位滞后等问题,寻找合适的缓蚀剂及其用量调配电解液以提高电池的放电性能。通过腐蚀浸泡试验表征了缓蚀剂Li_(2)CrO_(4)的缓蚀效果,然后通过极化曲线、电化学阻抗谱研究了Mg(ClO_(4))_(2)溶液中Li_(2)CrO_(4)用量对AZ31镁合金电化学性能的影响,最后通过组装水系镁锰电池进行恒流放电作为应用端测试。结果表明:Li_(2)CrO_(4)能够使AZ31镁合金的腐蚀电位正移,最大正移量达到150 m V,在水系镁锰电池应用中能够提高镁电池的放电平台,当Li_(2)CrO_(4)质量分数为0.7%时放电平台提高0.15 V左右;当Li_(2)CrO_(4)质量分数为1.2%时,其能够显著改善AZ31镁合金在Mg(ClO_(4))_(2)溶液中的腐蚀,水系镁锰电池放电容量达最大,为196.9 m A·h,相对空白溶液,电池的放电容量提高约64%,工作电压高达1.39 V且放电曲线稳定。展开更多
Although lithium-sulfur batteries(LSBs)exhibit high theoretical energy density,their practical application is hindered by poor conductivity of the sulfur cathode,the shuttle effect,and the irreversible deposition of L...Although lithium-sulfur batteries(LSBs)exhibit high theoretical energy density,their practical application is hindered by poor conductivity of the sulfur cathode,the shuttle effect,and the irreversible deposition of Li_(2)S.To address these issues,a novel composite,using electrospinning technology,consisting of Fe_(3)Se_(4)and porous nitrogen-doped carbon nanofibers was designed for the interlayer of LSBs.The porous carbon nanofiber structure facilitates the transport of ions and electrons,while the Fe_(3)Se_(4)material adsorbs lithium polysulfides(LiPSs)and accelerates its catalytic conversion process.Furthermore,the Fe_(3)Se_(4)material interacts with soluble LiPSs to generate a new polysulfide intermediate,Li_(x)FeS_(y)complex,which changes the electrochemical reaction pathway and facilitates the three-dimensional deposition of Li_(2)S,enhancing the reversibility of LSBs.The designed LSB demonstrates a high specific capacity of1529.6 mA h g^(-1)in the first cycle at 0.2 C.The rate performance is also excellent,maintaining an ultra-high specific capacity of 779.7 mA h g^(-1)at a high rate of 8 C.This investigation explores the mechanism of the interaction between the interlayer and LiPSs,and provides a new strategy to regulate the reaction kinetics and Li_(2)S deposition in LSBs.展开更多
Solving intrinsic structural problems such as low conductivity is the main challenge to promote the commercial application of Li_(2)TiSiO_(5).In this study,Li_(2)TiSiO_(5) is synthesized by the sol-gelmethod,and the s...Solving intrinsic structural problems such as low conductivity is the main challenge to promote the commercial application of Li_(2)TiSiO_(5).In this study,Li_(2)TiSiO_(5) is synthesized by the sol-gelmethod,and the surface modification of Li_(2)TiSiO_(5) is carried out at different temperatures using low-temperature plasma to enhance its lithium storage performance.The morphological structure and electrochemical tests demonstrate that plasma treatment can improve the degree of agglomeration.The peak position of the plasma-treated Li_(2)TiSiO_(5) is shifted to a lower angle,and the shift angle increases with increasing sputtering power.Li_(2)TiSiO_(5) after 300 W bombardment shows excellent capacity(144.7 mA·hg^(−1)after 500 cycles at 0.1 Ag^(−1))and rate performance(140 mA·hg^(−1)at 5 Ag^(−1)).Electrochemical analysis indicates that excellent electrochemical performance is attributed to the enhancement of electronic and ionic conductivity by plasma bombardment.展开更多
文摘针对AZ31镁合金作为镁电池负极时存在自腐蚀速率大、阳极极化、电位滞后等问题,寻找合适的缓蚀剂及其用量调配电解液以提高电池的放电性能。通过腐蚀浸泡试验表征了缓蚀剂Li_(2)CrO_(4)的缓蚀效果,然后通过极化曲线、电化学阻抗谱研究了Mg(ClO_(4))_(2)溶液中Li_(2)CrO_(4)用量对AZ31镁合金电化学性能的影响,最后通过组装水系镁锰电池进行恒流放电作为应用端测试。结果表明:Li_(2)CrO_(4)能够使AZ31镁合金的腐蚀电位正移,最大正移量达到150 m V,在水系镁锰电池应用中能够提高镁电池的放电平台,当Li_(2)CrO_(4)质量分数为0.7%时放电平台提高0.15 V左右;当Li_(2)CrO_(4)质量分数为1.2%时,其能够显著改善AZ31镁合金在Mg(ClO_(4))_(2)溶液中的腐蚀,水系镁锰电池放电容量达最大,为196.9 m A·h,相对空白溶液,电池的放电容量提高约64%,工作电压高达1.39 V且放电曲线稳定。
基金financially supported by the National Natural Science Foundation of China(No.22372103)Guangdong Basic and Applied Basic Research Foundation,China(2021A1515010241,2024A1515010032)the Shenzhen Science and Technology Foundation,China(JCYJ20220531103216037)。
文摘Although lithium-sulfur batteries(LSBs)exhibit high theoretical energy density,their practical application is hindered by poor conductivity of the sulfur cathode,the shuttle effect,and the irreversible deposition of Li_(2)S.To address these issues,a novel composite,using electrospinning technology,consisting of Fe_(3)Se_(4)and porous nitrogen-doped carbon nanofibers was designed for the interlayer of LSBs.The porous carbon nanofiber structure facilitates the transport of ions and electrons,while the Fe_(3)Se_(4)material adsorbs lithium polysulfides(LiPSs)and accelerates its catalytic conversion process.Furthermore,the Fe_(3)Se_(4)material interacts with soluble LiPSs to generate a new polysulfide intermediate,Li_(x)FeS_(y)complex,which changes the electrochemical reaction pathway and facilitates the three-dimensional deposition of Li_(2)S,enhancing the reversibility of LSBs.The designed LSB demonstrates a high specific capacity of1529.6 mA h g^(-1)in the first cycle at 0.2 C.The rate performance is also excellent,maintaining an ultra-high specific capacity of 779.7 mA h g^(-1)at a high rate of 8 C.This investigation explores the mechanism of the interaction between the interlayer and LiPSs,and provides a new strategy to regulate the reaction kinetics and Li_(2)S deposition in LSBs.
基金supported by Changzhou Basic Research Program(No.CJ20235030)the Research Initiation Fund of Changzhou University(No.ZMF23020057).
文摘Solving intrinsic structural problems such as low conductivity is the main challenge to promote the commercial application of Li_(2)TiSiO_(5).In this study,Li_(2)TiSiO_(5) is synthesized by the sol-gelmethod,and the surface modification of Li_(2)TiSiO_(5) is carried out at different temperatures using low-temperature plasma to enhance its lithium storage performance.The morphological structure and electrochemical tests demonstrate that plasma treatment can improve the degree of agglomeration.The peak position of the plasma-treated Li_(2)TiSiO_(5) is shifted to a lower angle,and the shift angle increases with increasing sputtering power.Li_(2)TiSiO_(5) after 300 W bombardment shows excellent capacity(144.7 mA·hg^(−1)after 500 cycles at 0.1 Ag^(−1))and rate performance(140 mA·hg^(−1)at 5 Ag^(−1)).Electrochemical analysis indicates that excellent electrochemical performance is attributed to the enhancement of electronic and ionic conductivity by plasma bombardment.
