Dipole-Gated Solvation Strategy for High-Rate Mg-Metal Batteries
Source abstract
Abstract
Developing high-performance next-generation energy storage systems is crucial for clean energy technologies. Mg-metal batteries are promising owing to their high specific capacity, high safety, and cost-effectiveness. However, the high charge density of Mg 2+ triggers strong Mg 2+ –ligand coordination, resulting in sluggish desolvation kinetics and poor rate performance. Here, we propose a dipole-gated solvation strategy and employ artificial-intelligence-driven clustering screening to construct solvation structures with large dipole moments. The weakly coordinating ligands preferentially approach the electrode via electric field–dipole interaction, enabling a dipole-gated effect that accelerates desolvation. This rapid desolvation also endows an ultrathin and uniform solid–electrolyte interphase, facilitating fast interfacial Mg 2+ transport. Consequently, the Mg-metal coin cell achieves rate capability up to 10C, while the Mg-metal pouch cell sustains stable cycling for over 400 cycles at 4C. This work advances multivalent batteries toward practical energy storage systems.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Advancements in Battery Materials · Thermal Expansion and Ionic Conductivity · Superconductivity in MgB2 and Alloys
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Beijing National Laboratory for Molecular Sciences, College of Chemistry and Molecular Engineering
Peking University
Academy for Advanced Interdisciplinary Studies
High Energy Photon Source, Institute of High Energy Physics
Chinese Academy of Sciences
Key Laboratory of Power Station Energy Transfer Conversion and Systems of Ministry of Education
North China Electric Power University
Funding
National Natural Science Foundation of China
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