Enhanced Thermal Transport across the Interface between Charged Graphene Electrodes and Poly(ethylene oxide) Electrolytes by Non-covalent Functionalization
Siyu Tian, Dezhao Huang, Zhihao Xu, Shiwen Wu, Tengfei Luo, Guoping, Xiong

TL;DR
This study uses molecular dynamics simulations to show that ionic liquids can non-covalently functionalize charged graphene electrodes, significantly improving interfacial thermal conductance in solid-state lithium-ion batteries during operation.
Contribution
It reveals how ionic liquids self-assemble at electrode surfaces and enhance thermal transport through increased LJ interactions, providing new insights into battery interface management.
Findings
ILs form dense interfacial layers on electrodes
Enhanced ITC during charge/discharge due to IL layers
Electrostatic and LJ interactions drive interfacial layer formation
Abstract
Interfacial thermal transport between electrodes and polymer electrolytes can play a crucial role in the thermal management of solid-state lithium-ion batteries (SLIBs). Modifying the electrode surface with functional molecules can effectively increase the interfacial thermal conductance (ITC) between electrodes and polymers (e.g., electrolytes, separators); however, how they influence the interfacial thermal transport in SLIBs during charge/discharge remains unknown. In this work, we conduct molecular dynamics (MD) simulations to investigate the ITC between charged electrodes and solid-state polymer electrolytes (SPEs) mixed with ionic liquids (ILs). We find that ILs could self assemble at the electrode surface and act as non-covalent functional molecules that could significantly enhance the interfacial thermal transport during charge/discharge because of the formation of a densely…
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Taxonomy
TopicsAdvancements in Battery Materials · Advanced Battery Materials and Technologies · Advanced Battery Technologies Research
