Related Experiment Video
Updated: Sep 19, 2026

Characterization of Electrode Materials for Lithium Ion and Sodium Ion Batteries Using Synchrotron Radiation Techniques
Published on: November 11, 2013
A paradigm shift in all-solid-state lithium batteries: halide cathode materials streamlined for multi-electron
Yang Luo1, Yuhao Duan2,3, Xiaofei Yang2,4
1School of Energy and Environmental Engineering, Hebei University of Technology, Tianjin 300401, China.
Abstract:
Halide cathode active materials (CAMs) are emerging as a transformative platform for all-solid-state lithium batteries (ASSLBs), offering intrinsic high ionic/electronic conductivities, multi-electron transfer capability and the unique potential for single-phase electrode architectures that eliminate inactive components. Despite these advantages, critical challenges regarding their reaction mechanisms, interfacial stability and structural evolution during cycling remain inadequately addressed. In this review, we systematically trace the evolution of halide CAMs from liquid electrolyte systems to ASSLBs, focusing on recent breakthroughs in single-phase interface engineering and multi-electron reaction mechanisms. We highlight how elemental and structural units govern ionic/electronic transport pathways and reversibility, while critically evaluating the dilemma between energy density and efficiency in the multi-electron reaction. Looking forward, a roadmap for next-generation halide CAM development is outlined, encompassing high-throughput material screening, controllable design of integrated all-in-one architectures and strategies to overcome voltage hysteresis and conversion kinetics limitations. By bridging fundamental insights with practical engineering, this review aims to provide actionable guidance for realizing high-energy, cost-effective ASSLBs.
Related Concept Videos
Batteries and Fuel Cells
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...

