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Synthesis of Bimetallic Pt/Sn-based Nanoparticles in Ionic Liquids
Published on: August 23, 2018
Microstructural evolution of tin nanoparticles during in situ sodium insertion and extraction
Jiang Wei Wang1, Xiao Hua Liu, Scott X Mao
1Department of Mechanical Engineering and Materials Science, University of Pittsburgh, Pittsburgh, Pennsylvania 15261, USA.
Nano Letters
|October 25, 2012
Summary
Tin nanoparticles undergo a two-step sodiation process in sodium ion batteries, forming amorphous alloys and then crystalline Na(15)Sn(4) with significant but manageable expansion. This demonstrates tin
Area of Science:
- Materials Science
- Electrochemistry
- Nanotechnology
Background:
- Tin (Sn) nanoparticles are promising anode materials for sodium-ion batteries.
- Understanding their electrochemical behavior, particularly during sodiation, is crucial for battery development.
Purpose of the Study:
- To investigate the microstructural changes and phase transformations of tin nanoparticles during electrochemical sodiation.
- To elucidate the mechanisms governing sodiation and volume expansion in Sn nanoparticles.
Main Methods:
- In situ transmission electron microscopy (TEM) was employed to observe nanosized tin nanoparticles within a sodium ion battery.
- Electrochemical sodiation and desodiation cycles were performed to study the material's response.
Main Results:
- Sodiation occurred in two distinct steps: a two-phase mechanism forming an amorphous Na-Sn alloy, followed by a single-phase mechanism leading to crystallized Na(15)Sn(4).
- Significant volumetric expansion (up to 420%) was observed, but cracking was mitigated by the single-phase sodiation mechanism accommodating stress.
- Excellent cyclability was achieved during reversible sodiation/desodiation.
Conclusions:
- Tin nanoparticles exhibit robust performance as electrode materials for rechargeable batteries.
- The unique two-step sodiation mechanism, particularly the stress-accommodating single-phase transformation, enhances the cyclability of tin nanoparticles.

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