RESEARCH

EMDL Research Portfolio


Updated 2024-05-12

Ultrathin, large-area Li-metal anodes

Rethinking the starting lithium metal anodesLithium (Li) metal has been considered an ideal anode material due to its superiority: the lowest electronegativity (-3.04 V) and ultrahigh specific capacity (3,860 mAh/g). However, it has plagued the practical applications due to key challenges: Li dendrite formation and electrolyte depletion. In particular, the dendritic growth of Li metal during the electrochemical plating process results in a dynamic evolution of its morphology and surface chemical nature. Therefore, a full understanding of the interface chemistry between electrode and electrolyte, i.e., solid-electrolyte interphase (SEI), is paramount. With advanced analysis tools, multi-scale investigations from an atomic structure (below nano) to bulk (micron scale) are highly required to reveal the basic fundamentals inside.

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Intelligent nano-colloid electrolytes

Beyond classical liquid electrolytes — Tailoring the Li+ microenvironment is crucial for achieving fast ionic transfer and a mechanically reinforced solid–electrolyte interphase (SEI), which administers the stable cycling of secondary batteries. Apart from traditional salt/solvent compositional tuning, we have provided some approaches for the simultaneous modulation of Li+ transport and SEI chemistry using functional nanomaterials dispersed in the liquid electrolytes. 

Homogeneous and fast Li+ transport towards the Li surface is required for uniform and dendrite-free deposition. Moving apart from a classic ionic transport of static liquid electrolytes involving electromigration and molecular diffusion can trigger a greater disparity in the Li concentration over the Li surface. To overcome this inherent problem, we invented a convective Li+ transfer for suppressing dendrite growth through magnetic nanospinbar (NSB)-dispersed colloidal electrolytes.

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Seamless charging Li-ion in extreme conditions

Pushing the limits of charging ratesCell engineering has been advanced to higher specific energy density by many battery researchers in the academy and industry for the long driving mileage of battery-powered EVs. In particular, building up the thick and dense electrode on the unit area of the Cu current collector is a successful method for gaining a lightweight capacity battery. Nevertheless, this current cell design is a bottleneck to fast charging due to cell polarization from limited Li diffusion by volume change, and it easily breaks and newly forms the SEI layer; depletion of Li+ source leads to radical capacity fading. To overcome cell polarization for the popularization of fast chargeable EVs, designing innovative materials and interface chemistry is crucial in the battery industry.

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Imaging-driven battery diagnosis

Looking inside the batteryBuilding a safer battery has become a common goal of academia and industry. Although the small errors inside the cells trigger catastrophic failures, identifying local defects or damages without anatomizing the cells and diagnosing cell safety and degradation remain challenging. EMDL group has expertise in real-time, non-invasive magnetic field imaging (MFI) that signals the battery current-induced magnetic field to visualize the current flow of the Li-ion pouch cells. A high-speed, spatially resolved MFI scan successfully derives the current distribution pattern from the cells with different tab positioning at a current load. 

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Building safe, sustainable batteries

Safe, environmentally benign, cost-positive battery thingsInstead of a Li-ion battery that uses an organic solvent with high fire risk as an electrolyte, we conducted to ensure stability in a grid-scale battery system, such as ESS, by using an aqueous Zn-ion battery with water as an electrolyte. The huge challenges are hydrogen evolution reaction (HER) and notorious Zn dendrite growth. The water decomposition at the operating voltage of the battery generates hydrogen, resulting in by-products and decreasing utilization efficiency of Zn. Dendrites growing on zinc metal surfaces cause internal short circuits, reducing battery life.

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