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Visualization of electrochemically driven solid-state phase transformations using operando hard X-ray spectro-imaging
- Source :
- Nature Communications
- Publication Year :
- 2015
- Publisher :
- Springer Science and Business Media LLC, 2015.
-
Abstract
- In situ techniques with high temporal, spatial and chemical resolution are key to understand ubiquitous solid-state phase transformations, which are crucial to many technological applications. Hard X-ray spectro-imaging can visualize electrochemically driven phase transformations but demands considerably large samples with strong absorption signal so far. Here we show a conceptually new data analysis method to enable operando visualization of mechanistically relevant weakly absorbing samples at the nanoscale and study electrochemical reaction dynamics of iron fluoride, a promising high-capacity conversion cathode material. In two specially designed samples with distinctive microstructure and porosity, we observe homogeneous phase transformations during both discharge and charge, faster and more complete Li-storage occurring in porous polycrystalline iron fluoride, and further, incomplete charge reaction following a pathway different from conventional belief. These mechanistic insights provide guidelines for designing better conversion cathode materials to realize the promise of high-capacity lithium-ion batteries.<br />Hard X-ray spectro-imaging using synchrotron radiation can be used to monitor electrochemical reactions. Here, the authors present X-ray absorption data and resolve phase evolution for the conversion of iron fluoride, a high-capacity Li-ion battery conversion cathode, with nanoscale resolution.
- Subjects :
- Battery (electricity)
Multidisciplinary
Materials science
Resolution (electron density)
X-ray
General Physics and Astronomy
Synchrotron radiation
Nanotechnology
General Chemistry
Electrochemistry
Article
General Biochemistry, Genetics and Molecular Biology
Cathode
law.invention
law
Phase (matter)
Absorption (electromagnetic radiation)
Subjects
Details
- ISSN :
- 20411723
- Volume :
- 6
- Database :
- OpenAIRE
- Journal :
- Nature Communications
- Accession number :
- edsair.doi.dedup.....030ebb3a766eac3802e0e12c6faf901b
- Full Text :
- https://doi.org/10.1038/ncomms7883