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Strongly coupled Te-SnS_(2)/MXene superstructure with self-autoadjustable function for fast and stable potassium ion storage 被引量:3
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作者 Hongyang Sun Yelong Zhang +12 位作者 Xiaodan Xu Jianwen Zhou Fan Yang Hao Li Hao Chen Yucheng Chen Zheng Liu Zhenping Qiu Da Wang Lipo Ma Jiawei Wang Qingguang Zeng Zhangquan Peng 《Journal of Energy Chemistry》 SCIE EI CAS CSCD 2021年第10期416-424,I0011,共10页
Potassium-ion batteries(PIBs)are a promising candidate for next-generation electric energy storage applications because of the abundance and low cost of potassium.However,the development of PIBs is limited by sluggish... Potassium-ion batteries(PIBs)are a promising candidate for next-generation electric energy storage applications because of the abundance and low cost of potassium.However,the development of PIBs is limited by sluggish kinetics and huge volume expansion of anodes,leading to poor rate capability and cycling stability.Herein,an advanced superstructure anode,including Te-doped SnS_(2) nanosheets uniformly anchored on MXene surface(Te-SnS_(2)/MXene),is rationally designed for the first time to boost K^(+)storage performance.Featuring with strong interface interaction and self-autoadjustable interlayer spacings,the Te-SnS_(2)/MXene can efficiently accelerate electron/ion transfer,accommodate volume expansion,inhibit crack formation,and improve pseudocapacitive contribution during cycling.Thus,the novel Te-SnS_(2)/MXene anode delivers a high reversible capacity(343.2 mAh g^(-1) after 50 cycles at0.2 A g^(-1)),outstanding rate capability(186.4 mAh g^(-1) at 20 A g^(-1)),long cycle stability(165.8 mAh g^(-1)after 5000 cycles at 10 A g^(-1) with a low electrode swelling rate of only 15.4%),and reliable operation in flexible full battery.The present Te-SnS_(2)/MXene becomes among the best transition metal-based anode materials for PIBs reported to date. 展开更多
关键词 Tin disulfide MXene Tellurium doping Potassium-ion battery
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LiOH: A "double-edged" effect toward electrochemical oxidation of Li_(2)O_(2)
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作者 Qinghua Cui Lipo Ma +2 位作者 Peng Zhang Yuliang Cao Jiawei Wang 《Journal of Energy Chemistry》 SCIE EI CAS CSCD 2021年第6期401-405,I0010,共6页
The aprotic lithium-oxygen battery(Li-O_(2) battery) has attracted much attraction for the future advanced battery technologies due to its ultra-high theoretical energy density that can well meet the ever-growing ener... The aprotic lithium-oxygen battery(Li-O_(2) battery) has attracted much attraction for the future advanced battery technologies due to its ultra-high theoretical energy density that can well meet the ever-growing energy demand of portable electronic products,electric vehicles(EVs),smart grids,and so on [1-5].In principle. 展开更多
关键词 Lithium-oxygen batteries LiOH-doped Li_(2)O_(2) Li_(2)O_(2)oxidation Differential electrochemical mass SPECTROMETER Isotope-labelling
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Unraveling the decomposition mechanism of Li_(2)CO_(3)in the aprotic medium by isotope-labeled differential electrochemical mass spectrometry
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作者 Lipo Ma Aiping Wang +2 位作者 Shoufeng Zhang Peng Zhang Jiawei Wang 《Journal of Energy Chemistry》 SCIE EI CAS CSCD 2022年第10期1-4,I0001,共5页
Rechargeable lithium-ion batteries(LIBs)represent the highest energy density in the contemporary energy storage community,typically delivering a practical energy density of 150-350 Wh kg-1in the current technique,whic... Rechargeable lithium-ion batteries(LIBs)represent the highest energy density in the contemporary energy storage community,typically delivering a practical energy density of 150-350 Wh kg-1in the current technique,which can hardly satisfy the evergrowing demand for the portable electronic devices and power tools requiring long service time[1-3]. 展开更多
关键词 Li_(2)CO_(3)electrochemistry Differential electrochemical mass spectrometry Isotope-label Reaction mechanism Electrode|electrolyte interface
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弹性MXene上垂直生长缺陷1T′-ReSe2纳米片实现快速稳定钾离子存储 被引量:1
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作者 周健文 张业龙 +8 位作者 刘争 邱振平 汪达 曾庆光 杨超 许冠南 杨勇 彭章泉 郭少军 《Science China Materials》 SCIE EI CAS CSCD 2022年第12期3418-3427,共10页
过渡金属二硫族化合物(TMDs)用作钾离子电池(KIBs)负极时存在反应动力学缓慢及结构稳定性不足等难题,导致其循环和倍率性能差,使得其应用严重受限.在本文中,我们将Te掺杂的1T′-ReSe_(2)负载在MXene上构建了高性能KIBs负极(Te-ReSe_(2)/... 过渡金属二硫族化合物(TMDs)用作钾离子电池(KIBs)负极时存在反应动力学缓慢及结构稳定性不足等难题,导致其循环和倍率性能差,使得其应用严重受限.在本文中,我们将Te掺杂的1T′-ReSe_(2)负载在MXene上构建了高性能KIBs负极(Te-ReSe_(2)/MXene).该超结构利用缺陷化的Te-ReSe_(2)与自调节弹性MXene的协同效应,表现出高可逆容量(0.1 A g^(−1)电流密度下循环200圈后为361.1 mA h g^(−1)),优异的倍率性能(20 A g^(−1)电流密度下为179.3 mA h g^(−1))和超长的循环寿命(5 A g^(−1)电流密度下循环2000圈后为202.8 mA h g^(−1)),并能实现柔性全电池的稳定运行,是目前所有TMDs基负极展示的最好性能之一.动力学分析和理论计算表明,该材料具有出色的赝电容特性,高电导率和优异的K^(+)吸附/扩散能力,显著提升了其反应动力学. 展开更多
关键词 循环寿命 倍率性能 全电池 赝电容 反应动力学 钾离子 超结构 扩散能力
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