Related Experiment Video
Updated: Oct 17, 2025

Synthesis of Ionic Liquid Based Electrolytes, Assembly of Li-ion Batteries, and Measurements of Performance at High Temperature
Published on: December 20, 2016
Enhancement of the ionic conductivity of lithium borohydride by silica supports
Guoyu Yang1, Chen Xie1, Yongtao Li1
1School of Materials Science and Engineering, Anhui University of Technology, Maanshan 243002, China. toni-li@163.com.
Abstract:
Confinement of LiBH4 in porous materials is an efficient route to enhance the ionic conductivity of lithium, which seems to be associated with various types of scaffolding and its mixture ratios. In the present work, we reveal the effect of supports on ionic conductivity improvements based on a comparison of different silica supports, including micro-SiO2 (SM), porous nano-SiO2 (MSN), and nano-SiO2 with nanochannels (SBA-15). All LiBH4/silica composites exhibited higher lithium ionic conductivity, where LiBH4/SBA-15 (47% weight ratio) exhibited the highest conductivity of 3 × 10-5 S cm-1 at 35 °C, nearly three orders of magnitude higher than that of pure LiBH4. In addition, the LiBH4/SBA-15 composite has a wider electrochemical stability window of -0.2 to 5 V, satisfactory compatibility with the Li anode, and no occurrence of side reactions. These ionic conductivity enhancements can be attributed to the support effects of distinct SiO2, i.e., the increase in surface area for superior interfacial ionic conductivity and/or the increased disorder of LiBH4 for faster matrix ionic conductivity. The present study offers useful insights for designing a new hydride solid electrolyte for all-solid-state lithium ion batteries.
Related Concept Videos
Formation of Complex Ions
Acid Halides to Alcohols: LiAlH4 Reduction
The mechanism proceeds in three steps. First, the nucleophilic hydride ion attacks the carbonyl carbon of the acid halide to form a tetrahedral intermediate. Next, the carbonyl group is re-formed, and the halide ion departs as a leaving group, generating an aldehyde. A second nucleophilic attack by the hydride yields an alkoxide ion, which, upon protonation, gives a primary alcohol as...

