Complex Hydride Solid Electrolytes of the Li(CB9H10)–Li(CB11H12) Quasi-Binary System: Relationship between the Solid Solution and Phase Transition, and the Electrochemical Properties

Closo-type complex hydrides have recently received much attention as promising solid electrolyte systems for all-solid-state batteries, because of the high lithium ion conductivity of their high-temperature (high-T) phases, excellent stability against a lithium metal anode, and a highly deformable n...

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Veröffentlicht in:ACS applied energy materials 2020-05, Vol.3 (5), p.4831-4839
Hauptverfasser: Kim, Sangryun, Kisu, Kazuaki, Takagi, Shigeyuki, Oguchi, Hiroyuki, Orimo, Shin-ichi
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Kisu, Kazuaki
Takagi, Shigeyuki
Oguchi, Hiroyuki
Orimo, Shin-ichi
description Closo-type complex hydrides have recently received much attention as promising solid electrolyte systems for all-solid-state batteries, because of the high lithium ion conductivity of their high-temperature (high-T) phases, excellent stability against a lithium metal anode, and a highly deformable nature. However, the superionic conductivity of closo-type complex hydrides is achieved in only a few materials; therefore, an understanding of the material factors involved in the formation of the high-T phase at room temperature and experimental demonstration of their battery applications are required. Here, we report the relationship between the solid solution and formation of the high-T phase of the Li­(CB9H10)–Li­(CB11H12) quasi-binary system, and the electrochemical properties as a solid electrolyte for all-solid-state Li–TiS2 batteries. The single-phase solid solutions, Li­(CB9H10)-based phase in which [CB9H10]− is partially substituted with [CB11H12]− and Li­(CB11H12)-based phase in which [CB11H12]− is partially substituted with [CB9H10]−, are obtained at compositions with low- and high-x in the (1 – x)­Li­(CB9H10)–xLi­(CB11H12) (0.1 ≤ x ≤ 0.9) system. The effect of the solid solution on structural changes is more noticeable at low x, whereby a superionic conducting phase is formed with an identical structural framework as that of the high-T phase of Li­(CB9H10) at room temperature. In addition, the 0.7Li­(CB9H10)–0.3Li­(CB11H12) (x = 0.3) solid electrolyte exhibits high chemical/electrochemical stability against a TiS2 cathode, which leads to superior performance in the rate capability and cycle life of all-solid-state Li–TiS2 batteries. The results presented here offer insights into strategies for the design of complex hydride lithium superionic conductors and for the development of all-solid-state batteries with these solid electrolytes.
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However, the superionic conductivity of closo-type complex hydrides is achieved in only a few materials; therefore, an understanding of the material factors involved in the formation of the high-T phase at room temperature and experimental demonstration of their battery applications are required. Here, we report the relationship between the solid solution and formation of the high-T phase of the Li­(CB9H10)–Li­(CB11H12) quasi-binary system, and the electrochemical properties as a solid electrolyte for all-solid-state Li–TiS2 batteries. The single-phase solid solutions, Li­(CB9H10)-based phase in which [CB9H10]− is partially substituted with [CB11H12]− and Li­(CB11H12)-based phase in which [CB11H12]− is partially substituted with [CB9H10]−, are obtained at compositions with low- and high-x in the (1 – x)­Li­(CB9H10)–xLi­(CB11H12) (0.1 ≤ x ≤ 0.9) system. The effect of the solid solution on structural changes is more noticeable at low x, whereby a superionic conducting phase is formed with an identical structural framework as that of the high-T phase of Li­(CB9H10) at room temperature. In addition, the 0.7Li­(CB9H10)–0.3Li­(CB11H12) (x = 0.3) solid electrolyte exhibits high chemical/electrochemical stability against a TiS2 cathode, which leads to superior performance in the rate capability and cycle life of all-solid-state Li–TiS2 batteries. 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Energy Mater</addtitle><description>Closo-type complex hydrides have recently received much attention as promising solid electrolyte systems for all-solid-state batteries, because of the high lithium ion conductivity of their high-temperature (high-T) phases, excellent stability against a lithium metal anode, and a highly deformable nature. However, the superionic conductivity of closo-type complex hydrides is achieved in only a few materials; therefore, an understanding of the material factors involved in the formation of the high-T phase at room temperature and experimental demonstration of their battery applications are required. Here, we report the relationship between the solid solution and formation of the high-T phase of the Li­(CB9H10)–Li­(CB11H12) quasi-binary system, and the electrochemical properties as a solid electrolyte for all-solid-state Li–TiS2 batteries. The single-phase solid solutions, Li­(CB9H10)-based phase in which [CB9H10]− is partially substituted with [CB11H12]− and Li­(CB11H12)-based phase in which [CB11H12]− is partially substituted with [CB9H10]−, are obtained at compositions with low- and high-x in the (1 – x)­Li­(CB9H10)–xLi­(CB11H12) (0.1 ≤ x ≤ 0.9) system. The effect of the solid solution on structural changes is more noticeable at low x, whereby a superionic conducting phase is formed with an identical structural framework as that of the high-T phase of Li­(CB9H10) at room temperature. In addition, the 0.7Li­(CB9H10)–0.3Li­(CB11H12) (x = 0.3) solid electrolyte exhibits high chemical/electrochemical stability against a TiS2 cathode, which leads to superior performance in the rate capability and cycle life of all-solid-state Li–TiS2 batteries. 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Energy Mater</addtitle><date>2020-05-26</date><risdate>2020</risdate><volume>3</volume><issue>5</issue><spage>4831</spage><epage>4839</epage><pages>4831-4839</pages><issn>2574-0962</issn><eissn>2574-0962</eissn><abstract>Closo-type complex hydrides have recently received much attention as promising solid electrolyte systems for all-solid-state batteries, because of the high lithium ion conductivity of their high-temperature (high-T) phases, excellent stability against a lithium metal anode, and a highly deformable nature. However, the superionic conductivity of closo-type complex hydrides is achieved in only a few materials; therefore, an understanding of the material factors involved in the formation of the high-T phase at room temperature and experimental demonstration of their battery applications are required. Here, we report the relationship between the solid solution and formation of the high-T phase of the Li­(CB9H10)–Li­(CB11H12) quasi-binary system, and the electrochemical properties as a solid electrolyte for all-solid-state Li–TiS2 batteries. The single-phase solid solutions, Li­(CB9H10)-based phase in which [CB9H10]− is partially substituted with [CB11H12]− and Li­(CB11H12)-based phase in which [CB11H12]− is partially substituted with [CB9H10]−, are obtained at compositions with low- and high-x in the (1 – x)­Li­(CB9H10)–xLi­(CB11H12) (0.1 ≤ x ≤ 0.9) system. The effect of the solid solution on structural changes is more noticeable at low x, whereby a superionic conducting phase is formed with an identical structural framework as that of the high-T phase of Li­(CB9H10) at room temperature. In addition, the 0.7Li­(CB9H10)–0.3Li­(CB11H12) (x = 0.3) solid electrolyte exhibits high chemical/electrochemical stability against a TiS2 cathode, which leads to superior performance in the rate capability and cycle life of all-solid-state Li–TiS2 batteries. The results presented here offer insights into strategies for the design of complex hydride lithium superionic conductors and for the development of all-solid-state batteries with these solid electrolytes.</abstract><pub>American Chemical Society</pub><doi>10.1021/acsaem.0c00433</doi><tpages>9</tpages><orcidid>https://orcid.org/0000-0001-8617-3022</orcidid><orcidid>https://orcid.org/0000-0002-1693-4225</orcidid></addata></record>
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