In Situ Formed Li–B–H Complex with High Li-Ion Conductivity as a Potential Solid Electrolyte for Li Batteries

2019 ◽  
Vol 11 (15) ◽  
pp. 14136-14141 ◽  
Author(s):  
Mengfei Zhu ◽  
Yuepeng Pang ◽  
Fuqiang Lu ◽  
Xinxin Shi ◽  
Junhe Yang ◽  
...  
2021 ◽  
Vol 369 ◽  
pp. 115713
Author(s):  
Xingxing Zhang ◽  
Cheng Li ◽  
Weili Liu ◽  
Tae-Sik Oh ◽  
Jeffrey W. Fergus

2015 ◽  
Vol 3 (42) ◽  
pp. 21343-21350 ◽  
Author(s):  
Stefan Breuer ◽  
Denise Prutsch ◽  
Qianli Ma ◽  
Viktor Epp ◽  
Florian Preishuber-Pflügl ◽  
...  

Impedance spectroscopy measurements down to very low temperatures allowed for resolving bulk ion transport properties in highly conducting ceramic electrolytes.


2016 ◽  
Vol 4 (18) ◽  
pp. 6972-6979 ◽  
Author(s):  
Beatriz Lopez-Bermudez ◽  
Wolfgang G. Zeier ◽  
Shiliang Zhou ◽  
Anna J. Lehner ◽  
Jerry Hu ◽  
...  

The development of new frameworks for solid electrolytes exhibiting fast Li-ion diffusion is critical for enabling new energy storage technologies.


2016 ◽  
Vol 113 (47) ◽  
pp. 13313-13317 ◽  
Author(s):  
Yutao Li ◽  
Weidong Zhou ◽  
Xi Chen ◽  
Xujie Lü ◽  
Zhiming Cui ◽  
...  

A solid electrolyte with a high Li-ion conductivity and a small interfacial resistance against a Li metal anode is a key component in all-solid-state Li metal batteries, but there is no ceramic oxide electrolyte available for this application except the thin-film Li-P oxynitride electrolyte; ceramic electrolytes are either easily reduced by Li metal or penetrated by Li dendrites in a short time. Here, we introduce a solid electrolyte LiZr2(PO4)3 with rhombohedral structure at room temperature that has a bulk Li-ion conductivity σLi = 2 × 10−4 S⋅cm−1 at 25 °C, a high electrochemical stability up to 5.5 V versus Li+/Li, and a small interfacial resistance for Li+ transfer. It reacts with a metallic lithium anode to form a Li+-conducting passivation layer (solid-electrolyte interphase) containing Li3P and Li8ZrO6 that is wet by the lithium anode and also wets the LiZr2(PO4)3 electrolyte. An all-solid-state Li/LiFePO4 cell with a polymer catholyte shows good cyclability and a long cycle life.


2019 ◽  
Vol 6 (16) ◽  
pp. 1900190 ◽  
Author(s):  
Boaz Moeremans ◽  
Hsiu‐Wei Cheng ◽  
Claudia Merola ◽  
Qingyun Hu ◽  
Mehtap Oezaslan ◽  
...  

2011 ◽  
Vol 2 (18) ◽  
pp. 2352-2356 ◽  
Author(s):  
Maria L. Sushko ◽  
Kevin M. Rosso ◽  
Ji-Guang (Jason) Zhang ◽  
Jun Liu

2017 ◽  
Vol 349 ◽  
pp. 105-110 ◽  
Author(s):  
Masashi Kotobuki ◽  
Shufeng Song ◽  
Rika Takahashi ◽  
Shunichi Yanagiya ◽  
Li Lu

RSC Advances ◽  
2021 ◽  
Vol 11 (48) ◽  
pp. 30283-30294
Author(s):  
Charlotte Fritsch ◽  
Tatiana Zinkevich ◽  
Sylvio Indris ◽  
Martin Etter ◽  
Volodymyr Baran ◽  
...  

Investigation of commercial Li7La3Zr2O12 (LLZO) with various substituents. Although impedance spectroscopy suggests something else: the ion conductivity does not show a strong dependence on the substituting cation, but rather on the sample treatment.


2020 ◽  
Author(s):  
Tingting Yang ◽  
Hui Li ◽  
Yongfu Tang ◽  
Jingzhao Chen ◽  
Hongjun Ye ◽  
...  

Abstract The growth of lithium (Li) whiskers is detrimental to Li batteries. However, it remains a challenge to directly track Li whisker growth. Here we report in situ observations of electrochemically induced Li deposition under a CO2 atmosphere inside an environmental transmission electron microscope. We find that the morphology of individual Li deposits is strongly influenced by the competing processes of cracking and self-healing of the solid electrolyte interphase (SEI). When cracking overwhelms self-healing, the directional growth of Li whiskers predominates. In contrast, when self-healing dominates over cracking, the isotropic growth of round Li particles prevails. The Li deposition rate and SEI constituent can be tuned to control the Li morphologies. We reveal a new “weak-spot” mode of Li dendrite growth, which is attributed to the operation of the Bardeen-Herring growth mechanism in the whisker’s cross section. This work has implications for the control of Li dendrite growth in Li batteries.


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