Abstract

Due to their high theoretical capacity compared to that of state-of-the-art graphite-based electrodes, silicon electrodes have gained much research focus for use in the development of next generation lithium-ion batteries. However, a major drawback of silicon as an electrode material is that it suffers from particle fracturing due to huge volume expansion during electrochemical cycling, thus limiting commercialization of such electrodes. Understanding the role of material microstructure in electrode degradation will be instrumental in the design of stable silicon electrodes. Here, we demonstrate the application of synchrotron-based X-ray tomographic microscopy to capture and track microstructural evolution, phase transformation and fracturing within a silicon-based electrode during electrochemical lithiation.

Highlights

  • Lithium-ion batteries are ubiquitous as power sources in portable electronic devices due to their high energy density and long cycle life, and are being extended to applications such as electric vehicles and grid energy storage [1,2]

  • Vertical and horizontal cross-sections through an X-ray tomogram of the half-cell assembly are presented in Fig. 2a; the horizontal section intersects the cell at the level of the Si electrode

  • The dense Si particles can be differentiated from the conductive matrix and electrolyte/pore phases by their higher X-ray attenuation

Read more

Summary

Introduction

Lithium-ion batteries are ubiquitous as power sources in portable electronic devices due to their high energy density and long cycle life, and are being extended to applications such as electric vehicles and grid energy storage [1,2]. To meet such demanding electronic applications, the development of highperformance lithium-ion batteries is crucial and significant research effort has been devoted to achieve this. Taiwo et al / Journal of Power Sources 342 (2017) 904e912 fracturing and pulverization, which results in loss of electrical contact and rapid capacity fading within the battery

Methods
Results
Conclusion

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.