Synthesis and Electrochemical Performances of Y-Doped Lithium-Rich Layered Li[Li0.2Ni0.2Mn0.6]O2Cathode Material
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Abstract
A series of lithium-rich cathode materials Li[Li 0.2 Ni 0.2− x /2 Mn 0.6− x /2 Y x ]O 2 ( x = 0, 0.01, 0.02, 0.03 and 0.05) were synthesized by the carbonate co-precipitation method. The influence of Y 3+ doping on the structural and morphological characterizations was examined by means of X-ray diffraction (XRD), inductively coupled plasma-atomic emission spectrometry (ICP-AES) and scanning electron microscopy (SEM). The results show that the crystal structure and morphology of the powders are not distinctly changed with the incorporation of Y ions. Charge-discharge tests show that materials doped with a proper amount of yttrium display good cycling stability and good rate capability, compared with un-doped material. When the doped content is 0.03 (Li[Li 0.2 Ni 0.185 Mn 0.585 Y 0.03 ]O 2 ), it delivers initial coulombic efficiency of 77.6%, a highly reversible capacity of 235.5 mAh g −1 and a capacity retention of 92.7% at the 50th cycle, which is much better than the pristine materials (74.8%, 185.5 mAh g −1 , and 81.0%). The cyclic voltammetry (CV) and AC impedance (EIS) results indicate that Y-doping can decrease electrochemical polarization and the charge-transfer resistance and enhance the ability of Li + diffusion in both the Li 2 MnO 3 and LiNi 1/2 Mn 1/2 O 2 components. Yttrium substitution is a convenient and effective method for improving the electrochemical performance of Lithium-rich layered Li[Li 0.2 Ni 0.2 Mn 0.6 ]O 2 cathode material.
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OpenAlex topics: Advancements in Battery Materials · Advanced Battery Materials and Technologies · Extraction and Separation Processes
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References (31)
Show source-provided references
1. 10.1016/j.electacta.2012.10.05410.1016/j.electacta.2012.10.054 ↗
2. 10.1016/j.elecom.2004.08.00210.1016/j.elecom.2004.08.002 ↗
3. 10.1016/j.jpowsour.2013.10.13910.1016/j.jpowsour.2013.10.139 ↗
4. 10.1016/j.electacta.2013.04.15010.1016/j.electacta.2013.04.150 ↗
5. 10.1039/b702425h10.1039/b702425h ↗
6. 10.1016/j.elecom.2009.01.02510.1016/j.elecom.2009.01.025 ↗
7. 10.1016/j.powtec.2013.02.03910.1016/j.powtec.2013.02.039 ↗
8. 10.1016/j.jpowsour.2011.12.04010.1016/j.jpowsour.2011.12.040 ↗
9. 10.1016/j.electacta.2012.06.11810.1016/j.electacta.2012.06.118 ↗
10. 10.1016/j.electacta.2014.06.15510.1016/j.electacta.2014.06.155 ↗
11. 10.1016/j.electacta.2016.01.06610.1016/j.electacta.2016.01.066 ↗
12. 10.1016/S0378-7753(03)00171-X10.1016/S0378-7753(03)00171-X ↗
13. 10.1016/S0378-7753(02)00400-710.1016/S0378-7753(02)00400-7 ↗
14. 10.1016/j.ceramint.2015.05.10210.1016/j.ceramint.2015.05.102 ↗
15. 10.1016/j.electacta.2005.07.02610.1016/j.electacta.2005.07.026 ↗
16. 10.1016/j.electacta.2013.05.14510.1016/j.electacta.2013.05.145 ↗
17. 10.1016/j.jallcom.2006.01.13210.1016/j.jallcom.2006.01.132 ↗
18. 10.1016/j.jpowsour.2007.01.07010.1016/j.jpowsour.2007.01.070 ↗
19. 10.1016/j.electacta.2015.05.06810.1016/j.electacta.2015.05.068 ↗
20. 10.1016/j.electacta.2015.03.22310.1016/j.electacta.2015.03.223 ↗
21. 10.1016/j.electacta.2010.08.02210.1016/j.electacta.2010.08.022 ↗
22. 10.1016/j.matchemphys.2005.09.08910.1016/j.matchemphys.2005.09.089 ↗
23. Rao · J. Power Sources · 2001 · 97 · 313
24. 10.1016/j.electacta.2010.07.06610.1016/j.electacta.2010.07.066 ↗
25. 10.1016/j.jpowsour.2005.08.02310.1016/j.jpowsour.2005.08.023 ↗
26. 10.1016/j.jallcom.2004.01.00810.1016/j.jallcom.2004.01.008 ↗
27. 10.1016/j.elecom.2006.11.00610.1016/j.elecom.2006.11.006 ↗
28. 10.1021/ja062027+10.1021/ja062027+ ↗
29. 10.1016/j.jpowsour.2012.12.04210.1016/j.jpowsour.2012.12.042 ↗
30. 10.1016/j.jpowsour.2004.08.04410.1016/j.jpowsour.2004.08.044 ↗
31. 10.1016/S0378-7753(00)00666-210.1016/S0378-7753(00)00666-2 ↗