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Modulating Nanoinhomogeneity at Electrode–Solid Electrolyte Interfaces for Dendrite-Proof Solid-State Batteries and Long-Life Memristors

机译:在电极 - 固体电解质界面调节纳米期性,用于树突式固态电池和长寿命忆阻器

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摘要

Dendrite penetration in ceramic lithium conductors severely constrains the development of solid-state batteries (SSBs) while its nanoscale origin remains unelucidated. An in situ nanoscopic electrochemical characterization technique is developed based on conductive-atomic force microscopy (c-AFM) to reveal the local dendrite growth kinetics. Using Li7La3Zr2O12 (LLZO) as a model system, significant local inhomogeneity is observed with a hundredfold decrease in the dendrite triggering bias at grain boundaries compared with that at grain interiors. The origin of the local weakening is assigned to the nanoscale variation of elastic modulus and lithium flux detouring. An ionic-conductive polymeric homogenizing layer is designed which achieves a high critical current density of 1.8 mA cm(-2) and a low interfacial resistance of 14 omega cm(2). Practical SSBs based on LiFePO4 cathodes can be stably cycled over 300 times. Beyond this, highly reversible electrochemical dendrite healing in LLZO is discovered using the c-AFM electrode, based on which a model memristor with a high on/off ratio of approximate to 10(5) is demonstrated for 200 cycles. This work not only provides a novel tool to investigate and design interfaces in SSBs but also offers opportunities for solid electrolytes beyond energy applications.
机译:陶瓷锂导体中的树突渗透严重限制了固态电池(SSB)的开发,而其纳米级源仍然是不酸化的。基于导电原子力显微镜(C-AFM)开发了一种原位纳米镜电化学表征技术,以揭示局部树突生长动力学。使用Li7La3zR2O12(LLZO)作为模型系统,与在晶粒间室内的晶界触发偏压下的百晶触发偏差下降,观察到显着的局部不均匀性。局部弱化的起源被分配给弹性模量和锂通量绕道的纳米级变型。设计了离子导电聚合物均化层,其实现了1.8 mA cm(-2)的高临界电流密度和14 uMega cm(2)的低界面抗性。基于LifePO4阴极的实用SSBS可以稳定地循环超过300次。除此之外,使用C-AFM电极发现LLZO中的高度可逆电化学枝晶愈合,基于该C-AFM电极,其具有高于10(5)的高开/关比的模型忆阻器被证明> 200个循环。这项工作不仅提供了一种新颖的工具来调查和设计SSB中的界面,但也为超出能源应用的固体电解质提供机会。

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