Effect of pH value on particle morphology and electrochemical properties of LiFePO4 by hydrothermal method
Source abstract
Abstract
Abstract Lithium iron phosphate was prepared by hydrothermal synthesis using LiOH·H2O, FeSO4·7H2O and H3PO4 as raw materials. The effects of pH value of reaction solution on particle morphology and electrochemical property were investigated. The pH value of the reaction solution was adjusted in the range of 2.5–8.8 by dilute sulfuric acid and ammonia water. The samples were characterized by field-emission scanning electronic microscope (FE-SEM), X-ray powder diffraction (XRD), constant-current charge/discharge cycling tests and chemical analysis. The results indicated that the particles exhibited acute angle diamond flake-like morphology at pH = 2.5, and as the pH value increased, the particle became hexagon flake-like, round flake-like and irregular flake-like morphology gradually. The optimal sample synthesized at pH = 6.4 exhibited discharge capacities of 151.8 mAh g−1 at 0.2 C rate and 129.3 mAh g−1 at 3 C rate. It was found that pH value affected the morphologies and properties of the product by means of different crystal growth rates.
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Research context
OpenAlex topics: Advancements in Battery Materials · Extraction and Separation Processes · Advanced Battery Technologies Research
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References (26)
Show source-provided references
1. Jin · J. Power Sources · 2008 · 178 · 80110.1016/j.jpowsour.2007.09.073 ↗
2. Kuwahara · Ceram. Int. · 2008 · 34 · 86310.1016/j.ceramint.2007.09.037 ↗
3. Liang · J. Power Sources · 2008 · 184 · 53810.1016/j.jpowsour.2008.02.056 ↗
4. Jin · Solid State Ionics · 2008 · 178 · 190710.1016/j.ssi.2007.12.057 ↗
5. Ramana · J. Power Sources · 2009 · 187 · 55510.1016/j.jpowsour.2008.11.042 ↗
6. Chen · Solid State Ionics · 2008 · 178 · 167610.1016/j.ssi.2007.10.015 ↗
7. Tajimi · Solid State Ionics · 2004 · 175 · 28710.1016/j.ssi.2003.12.033 ↗
8. Rangappa · J. Power Sources · 2010 · 195 · 616710.1016/j.jpowsour.2009.11.095 ↗
9. Rangappa · Chem. Commun. · 2010 · 46 · 754810.1039/c0cc03034a ↗
10. Rangappa · J. Power Sources · 2009 · 194 · 103610.1016/j.jpowsour.2009.06.042 ↗
11. Wang · J. Power Sources · 2009 · 189 · 54310.1016/j.jpowsour.2008.10.044 ↗
12. Zhang · Ceram. Int. · 2009 · 35 · 297910.1016/j.ceramint.2009.02.024 ↗
13. Jin · Electrochem. Commun. · 2008 · 10 · 153710.1016/j.elecom.2008.08.001 ↗
14. Chen · Electrochem. Commun. · 2006 · 8 · 85510.1016/j.elecom.2006.03.021 ↗
15. Wang · J. Power Sources · 2008 · 184 · 63310.1016/j.jpowsour.2008.04.066 ↗
16. Delacourt · Solid State Ionics · 2004 · 173 · 11310.1016/j.ssi.2004.07.061 ↗
17. Delacourt · Electrochem. Solid-State Lett. · 2006 · 9 · A35210.1149/1.2201987 ↗
18. Liu · J. Power Sources · 2009 · 194 · 53610.1016/j.jpowsour.2009.05.007 ↗
19. Aimiable · Solid State Ionics · 2009 · 180 · 86110.1016/j.ssi.2009.02.019 ↗
20. Lee · J. Supercrit. Fluids · 2005 · 35 · 8310.1016/j.supflu.2004.12.005 ↗
21. Dokko · J. Power Sources · 2007 · 165 · 65610.1016/j.jpowsour.2006.10.027 ↗
22. Yang · Chem. Commun. · 2001 · 3 · 505
23. Xu · J. Supercrit. Fluids · 2008 · 44 · 9210.1016/j.supflu.2007.09.001 ↗
24. G. Nuspl, L. Wimmer, M. Eisgruber, Canadian Patent Application CA2537278 (2005).
25. Chen · Electrochem. Solid-State Lett. · 2006 · 9 · A29510.1149/1.2192695 ↗
26. Fisher · J. Mater. Chem. · 2008 · 18 · 120910.1039/b715935h ↗