High rate capability by sulfur-doping into LiFePO matrix
RSC Advances, ISSN: 2046-2069, Vol: 8, Issue: 11, Page: 5848-5853
2018
- 53Citations
- 47Captures
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Example: if you select the 1-year option for an article published in 2019 and a metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019. If you select the 3-year option for the same article published in 2019 and the metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019, 2018 and 2017.
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Metrics Details
- Citations53
- Citation Indexes52
- 52
- CrossRef39
- Patent Family Citations1
- Patent Families1
- Captures47
- Readers47
- 47
Article Description
Enhanced electrochemical performance of LiFePO for Li-ion batteries has been anticipated by anion doping at the O-site rather than cation doping at the Fe-site. We report on the electrochemical performance of S-doped LiFePO nanoparticles synthesized by a solvothermal method using thioacetamide as a sulfur source. S-doping into the LiFePO matrix expands the lattice due to the larger ionic radius of S than that of O. The lattice parameters a and b increase by around 0.2% with sulfur content, while that of c remains almost unchanged with only 0.03% increase. The S-doping also contributes to the suppression of antisite defects (Fe occupying Li sites), which facilitates the easy migration of Li in the diffusion channels without blockage. Owing to these effects of S-doping, the S-doped LiFePO nanoparticles show enhanced electrochemical properties with a high discharge capacity of ∼113 mA h g even at a high rate of 10C.
Bibliographic Details
http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=85041864579&origin=inward; http://dx.doi.org/10.1039/c7ra12740e; http://www.ncbi.nlm.nih.gov/pubmed/35539603; https://xlink.rsc.org/?DOI=C7RA12740E; https://dx.doi.org/10.1039/c7ra12740e; https://pubs.rsc.org/en/content/articlelanding/2018/ra/c7ra12740e
Royal Society of Chemistry (RSC)
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