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Large Intercalation Pseudocapacitance in 2D VO2 (B): Breaking through the Kinetic Barrier
Chuan Xia1, Zifeng Lin2,3, Yungang Zhou4
1Materials Science and Engineering, Physical Sciences and Engineering Division, King Abdullah University of Science and Technology (KAUST), Thuwal, 23955-6900, Saudi Arabia.
Atomically thin, 2D vanadium dioxide (VO2) nanostructures enable a sluggish lithium-ion process at room temperature. This breakthrough enhances charge storage kinetics and reversibility in VO2 (B) materials.
Area of Science:
- Materials Science
- Electrochemistry
- Nanotechnology
Background:
- Vanadium dioxide (VO2) in its B phase exhibits two lithiation/delithiation processes.
- A facile process occurs at 2.5 V vs. Li/Li+, while a sluggish process at 2.1 V vs. Li/Li+ requires elevated temperatures due to high energy barriers.
Purpose of the Study:
- To investigate if rational design of atomically thin, 2D nanostructures can overcome kinetic limitations in VO2 (B).
- To enable the sluggish lithiation/delithiation process to occur at room temperature.
Main Methods:
- Fabrication of atomically thin, 2D nanostructures of VO2 (B).
- Characterization of ion diffusion barriers and interaction energies in the nanostructures.
- Electrochemical testing at room temperature.
Main Results:
- Atomically thin, 2D VO2 (B) nanostructures significantly reduce interaction energy and Li+ diffusion barriers.
- The kinetically sluggish process at 2.1 V vs. Li/Li+ is successfully activated at room temperature for the first time.
- The material demonstrates fast charge storage kinetics and fully reversible Li+ uptake/removal without phase change.
Conclusions:
- Rational design of 2D nanostructures is an effective strategy to accelerate intrinsically sluggish processes in non-van der Waals layered materials.
- This approach leads to exceptionally high performance in VO2 (B) for energy storage applications.
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