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Low Volume-Expansion, Insertion-Type Layered Silicate Hierarchical Structure For Superior Storage Of Li, Na, K

机译:低体积膨胀、插入式层状硅酸盐分层结构,可出色地储存 Li、Na、K

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摘要

A hierarchical structure is successfully synthesized by coating polypyrrole (PPy)on the surface of carbon/saponite superlattice (denoted as PPy@C/SAP), andapplied as low volume-expansion insertion-type anode for Li, Na, K storage.The synergistic effect of metal Ni, Fe doping, carbon/silicate superlattice,abundant oxygen vacancies and PPy coating leads to a good electronicconductivity and large current discharging capability. As a Si-based material,PPy@C/SAP has excellent storage capability for Li (659 mAh g~(?1) after1000 cycles at 2 A g~(?1) and 550 mAh g~(?1) after 1000 cycles at 5 A g~(?1)), Na(maximum specific capacity of 533 and 327 mAh g~(?1) after 50 cycles) as well asK (236 mAh g~(?1) after 100 cycles). XPS, XANES, XRD, FTIR, HRTEM, SEM areused to detect the hybrid mechanism (bulk insertion and surface conversion)with a volume expansion as low as 9. Insertion reaction driven by valencestate change of Ni, Fe, Si (Ni~0?Ni~(2+), Fe0?Fe~(3+), Si~(2+)?Si~(4+)) in laminates andconversion reactions between LiOH/Li2CO3 and LiH/Li_2C_2 catalyzed by Ni°contribute to the high performance. In the whole electrochemical process,layered structure is retained while the conversion reactions of LiOH (prodecedby laminates dehydroxylation) and Li2CO3 (electrolyte decomposition)cause the dynamic evolution of solid ectrolyte interphase. This study developsa promising Si-based anode material for lithium ion batteries, sodium ionbatteries and potassium ion batteries, which is significant for designing longcycle life rechargeable batteries.
机译:通过在碳/皂石超晶格表面包覆聚吡咯(PPy)成功合成了多级结构(表示为PPy@C/SAP),并作为低体积膨胀插入型阳极应用于Li、Na、K存储。金属Ni、Fe掺杂、碳/硅酸盐超晶格、丰富的氧空位和PPy涂层的协同作用导致了良好的导电性和大电流放电能力。作为硅基材料,PPy@C/SAP对Li(2 A g~(?1)循环1000次后为659 mAh g~(?1)和550 mAh g~(?1)在5 A g~(?1)下循环1000次后为550 mAh g~(?1)、Na(50次循环后最大比容量为533和327 mAh g~(?1))以及K(100次循环后为236 mAh g~(?1))具有优异的存储能力。XPS、XANES、XRD、FTIR、HRTEM、SEM用于检测体积膨胀低至9%的混合机制(批量插入和表面转换)。Ni、Fe、Si(Ni~0?Ni~(2+), Fe0?Fe~(3+), Si~(2+)?Si~(4+)))在Ni°的催化下,LiOH/Li2CO3与LiH/Li_2C_2之间的转化反应有助于提高其性能。在整个电化学过程中,层状结构得以保留,而LiOH(层压脱羟基化)和Li2CO3(电解质分解)的转化反应导致固体外解质界面的动态演化。本研究开发了一种很有前途的锂离子电池、钠离子电池和钾离子电池硅基负极材料,对设计长循环寿命可充电电池具有重要意义。

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