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Preparation of Metal-Oxide-Doped Li7P2S8Br0.25I0.75 Solid Electrolytes for All-Solid-State Lithium Batteries

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Abstract
The all-solid-state lithium battery (ASSB) has received great attention due to its greater safety than the conventional lithium-ion battery (LIB). Sulfide-based inorganic solid electrolytes are an important component to fabricate the ASSB. But to attain a better performance, the ionic conductivity and electrochemical stability of the sulfide-based solid electrolytes need to be improved. In this work, we prepared the metal-oxide-doped/mixed Li7P2S8I0.75Br0.25 lithium superionic conductors by a dry ball-milling process. The high ionic conductivity was achieved by a low-temperature (200 °C) heat-treatment process. The metal-oxide-doped Li7P2S8I0.75Br0.25 solid electrolyte exhibited a higher ionic conductivity value of 7.3 mS cm–1 at room temperature than the bare Li7P2S8I0.75Br0.25 solid electrolyte. The structural characteristics of the prepared solid electrolytes were studied by solid NMR and laser Raman analysis. The electrochemical stability of the prepared solid electrolyte was studied by cyclic voltammetry and DC charge–discharge analysis. The addition of metal oxide increased the electrochemical stability and dry-air stability of the Li7P2S8I0.75Br0.25 solid electrolyte. The Ta2O5-doped Li7P2S8I0.75Br0.25 solid electrolyte was stable even after 300 charge–discharge DC cycles and also 100 h of dry-air exposure. Further, the Ta2O5-doped Li7P2S8I0.75Br0.25 solid electrolyte-based ASSB exhibited a high discharge capacity value of 184 mA h g–1 at 0.1 C rate with 66% initial cycle Coulombic efficiency.
Issued Date
2023
Rajesh Rajagopal
Yuvaraj Subramanian
Yu Jin Jung
Sung Kang
Kwang-Sun Ryu
Type
Article
Keyword
solid electrolyteLi7P2S8I0.75Br0.25metal oxide dopinghigh ionic conductivitygradient layer
DOI
10.1021/acsami.3c01338
URI
https://oak.ulsan.ac.kr/handle/2021.oak/17552
Publisher
ACS Applied Materials & Interfaces
Language
영어
ISSN
1944-8244
Citation Volume
15
Citation Number
17
Citation Start Page
21016
Citation End Page
21026
Appears in Collections:
Natural Science > Chemistry
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