MgO-Decorated Few-Layered Graphene as an Anode for Li-Ion Batteries
Source abstract
Abstract
Combustion of magnesium in dry ice and a simple subsequent acid treatment step resulted in a MgO-decorated few-layered graphene (FLG) composite that has a specific surface area of 393 m(2)/g and an average pore volume of 0.9 cm(3)/g. As an anode material in Li-ion batteries, the composite exhibited high reversible capacity and excellent cyclic performance in spite of high first-cycle irreversible capacity loss. A reversible capacity as high as 1052 mAh/g was measured during the first cycle. Even at the end of the 60th cycle, more than 83% of the capacity could be retained. Cyclic voltammetry results indicated pseudocapacitance behavior due to electrochemical absorption and desorption of lithium ions onto graphene. An increase in the capacity has been observed during long-term cycling owing to electrochemical exfoliation of graphene sheets. Owing to its good thermal stability and superior cyclic performance with high reversible capacities, MgO-decked FLG can be an excellent alternative to graphite as an anode material in Li-ion batteries, after suitable modifications.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Advancements in Battery Materials · Graphene research and applications · Supercapacitor Materials and Fabrication
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
School of Engineering Sciences and Technology, University of Hyderabad, Gachibowli, Hyderabad 500046, India
Department of Physics, Advanced Batteries lab, National University of Singapore, Singapore 117542, Singapore
Department of Materials Science and Engineering, National University of Singapore, Singapore 117576, Singapore
Funding
National University of Singapore · University Grants Commission
References (48)
Show source-provided references
1. Yin S. · ACS Nano · 2011 · 5 · 383110.1021/nn2001728 ↗
2. Jang B. Z. · Nano Lett. · 2011 · 11 · 378510.1021/nl2018492 ↗
3. Zhao X. · ACS Nano · 2011 · 5 · 873910.1021/nn202710s ↗
4. Wu Z.-S. · ACS Nano · 2011 · 5 · 546310.1021/nn2006249 ↗
5. Petnikota S. · J. Solid State Electrochem. · 2014 · 18 · 94110.1007/s10008-013-2338-2 ↗
6. Chakrabarti A. · J. Mater. Chem. · 2011 · 21 · 949110.1039/c1jm11227a ↗
7. Zhou W. · Electrochem. Commun. · 2011 · 13 · 110210.1016/j.elecom.2011.07.006 ↗
8. Wang Z. · J. Electrochem. Soc. · 2002 · 149 · A46610.1149/1.1456919 ↗
9. Chen J. · Rare Met. · 2011 · 30 · 16610.1007/s12598-011-0218-4 ↗
10. Song M.-S. · J. Electrochem. Soc. · 2004 · 151 · A79110.1149/1.1710895 ↗
11. Mladenov M. · Electrochem. Commun. · 2001 · 3 · 41010.1016/S1388-2481(01)00192-8 ↗
12. Gnanaraj J. S. · Electrochem. Commun. · 2003 · 5 · 94010.1016/j.elecom.2003.08.012 ↗
13. Zhao H. · J. Power Sources · 2004 · 132 · 19510.1016/j.jpowsour.2004.01.036 ↗
14. Zhecheva E. · J. Power Sources · 2006 · 162 · 82310.1016/j.jpowsour.2005.07.063 ↗
15. Leo C. J. · Solid State Ionics · 2003 · 159 · 35710.1016/S0167-2738(03)00032-8 ↗
16. Liu Y. · J. Phys. Chem. Lett. · 2013 · 4 · 173710.1021/jz400491b ↗
17. Rotte N. K. · Chem. Eng. J. · 2014 · 258 · 41210.1016/j.cej.2014.07.065 ↗
18. Das A. · Bull. Mater. Sci. · 2008 · 31 · 57910.1007/s12034-008-0090-5 ↗
19. Berry V. · Carbon · 2013 · 62 · 110.1016/j.carbon.2013.05.052 ↗
20. Li D. · Nat. Nano · 2008 · 3 · 10110.1038/nnano.2007.451 ↗
21. Lotya M. · J. Am. Chem. Soc. · 2009 · 131 · 361110.1021/ja807449u ↗
22. Si Y. · Nano Lett. · 2008 · 8 · 167910.1021/nl080604h ↗
23. Kumar A. · ACS Nano · 2011 · 5 · 434510.1021/nn201527p ↗
24. Yoo E. · Nano Lett. · 2008 · 8 · 227710.1021/nl800957b ↗
25. Bhardwaj T. · J. Am. Chem. Soc. · 2010 · 132 · 1255610.1021/ja106162f ↗
26. Lian P. · Electrochim. Acta · 2010 · 55 · 390910.1016/j.electacta.2010.02.025 ↗
27. Landi B. J. · J. Phys. Chem. C · 2008 · 112 · 750910.1021/jp710921k ↗
28. Landi B. J. · Energy Environ. Sci. · 2009 · 2 · 63810.1039/b904116h ↗
29. Kawasaki S. · Carbon · 2009 · 47 · 108110.1016/j.carbon.2008.12.034 ↗
30. Landi B. J. · J. Nanosci. Nanotechnol. · 2009 · 9 · 340610.1166/jnn.2009.NS09 ↗
31. Vinayan B. P. · J. Mater. Chem. · 2012 · 22 · 994910.1039/c2jm16294f ↗
32. Aurbach D. · J. Power Sources · 2000 · 89 · 20610.1016/S0378-7753(00)00431-6 ↗
33. Zhu Y. · Adv. Mater. · 2010 · 22 · 390610.1002/adma.201001068 ↗
34. Sterrer M. · J. Phys. Chem. B · 2000 · 104 · 360110.1021/jp993924l ↗
35. Stark J. V. · Chem. Mater. · 1996 · 8 · 190410.1021/cm950583p ↗
36. Stoimenov P. K. · Langmuir · 2002 · 18 · 667910.1021/la0202374 ↗
37. Bakardjieva S. · Microsc. Microanal. · 2004 · 10 · 47610.1017/S1431927604881479 ↗
38. Ferrari A. C. · Nat. Nano · 2013 · 8 · 23510.1038/nnano.2013.46 ↗
39. Wang B. · Nanoscale · 2014 · 6 · 98610.1039/C3NR04611G ↗
40. Yang Z. · Ionics · 2014 · 20 · 16910.1007/s11581-013-0974-2 ↗
41. Zhamu A. · Energy Environ. Sci. · 2012 · 5 · 570110.1039/C2EE02911A ↗
42. Sato K. · Science · 1994 · 264 · 55610.1126/science.264.5158.556 ↗
43. Wu Y. · ACS Appl. Mater. Interfaces · 2013 · 5 · 1217510.1021/am404216j ↗
44. Simon P. · Nat. Mater. · 2008 · 7 · 84510.1038/nmat2297 ↗
45. Nazri G. A. · 2009
46. Lee E. · Nano Lett. · 2012 · 12 · 462410.1021/nl3019164 ↗
47. Suzuki T. · Carbon · 2003 · 41 · 193310.1016/S0008-6223(03)00178-7 ↗
48. Chan Y. · Nanoscale Res. Lett. · 2011 · 6 · 20310.1186/1556-276X-6-203 ↗