Heteroepitaxy-Induced Rutile VO2 with Abundantly Exposed (002) Facets for High Lithium Electroactivity
Source abstract
Abstract
Research on VO 2 cathodes for lithium ion batteries has been mainly focused on the VO 2 (B) phase. However, rutile VO 2 (M/R) has rarely been studied because of the intrinsically low lithium activity resulting from the highly anisotropic nature of lithium accommodation. Here, we demonstrate that heteroepitaxial engineering can be an effective strategy for activating the anisotropic electrode and developing kinetically superior electrodes. Appropriate lattice mismatch between the active material (VO 2 ) and conductive support (Sb:SnO 2 ) yields a coherent interface, where tensile strain aids preferential growth along the rutile c -axis as well as expansion in the ab plane and thereby the exposure of reactive (002) facets. The VO 2 –Sb:SnO 2 electrode exhibits high reversible capacity (350 mA h g –1 at 100 mA g –1 ) and ultrafast rate capability (196 mA h g –1 at 2000 mA g –1 ) with structural stability, which represents record-high performance compared with previous VO 2 reports, including those on other polymorphs such as VO 2 (A) and VO 2 (B).
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Transition Metal Oxide Nanomaterials · Advancements in Battery Materials · Supercapacitor Materials and Fabrication
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Department of Materials Science and Engineering, Seoul National University, Seoul 151-744, Korea
School of Civil, Environmental and Architectural Engineering, Korea University, Seoul, 136-713, Korea
School of Materials Science and Engineering, Kyungpook National University, 80 Daehakro, Bukgu, Daegu 41566, Korea
References (46)
Show source-provided references
1. 10.1038/373557a010.1038/373557a0 ↗
2. 10.1038/3510464410.1038/35104644 ↗
3. 10.1039/c2ee21892e10.1039/c2ee21892e ↗
4. 10.1021/ja309143810.1021/ja3091438 ↗
5. 10.1021/cr020731c10.1021/cr020731c ↗
6. 10.1039/b819629j10.1039/b819629j ↗
7. 10.1021/nl400001u10.1021/nl400001u ↗
8. 10.1021/nl504038s10.1021/nl504038s ↗
9. 10.1039/C5TA00594A10.1039/C5TA00594A ↗
10. 10.1002/adma.20140071910.1002/adma.201400719 ↗
11. 10.1021/nl504705z10.1021/nl504705z ↗
12. 10.1149/1.183744210.1149/1.1837442 ↗
13. 10.1039/C1RA00698C10.1039/C1RA00698C ↗
14. 10.1021/am400202v10.1021/am400202v ↗
15. 10.1016/j.ssi.2007.07.00310.1016/j.ssi.2007.07.003 ↗
16. 10.1557/jmr.2007.025510.1557/jmr.2007.0255 ↗
17. 10.1038/srep0932810.1038/srep09328 ↗
18. 10.1103/PhysRevB.65.23542310.1103/PhysRevB.65.235423 ↗
19. 10.1002/adma.20050272310.1002/adma.200502723 ↗
20. 10.1016/j.elecom.2006.09.02210.1016/j.elecom.2006.09.022 ↗
21. 10.1002/adma.20060249910.1002/adma.200602499 ↗
22. 10.1021/am504971h10.1021/am504971h ↗
23. 10.1021/ja100102y10.1021/ja100102y ↗
24. 10.1002/adma.20100157810.1002/adma.201001578 ↗
25. 10.1021/nl302783910.1021/nl3027839 ↗
26. 10.1038/nmat225110.1038/nmat2251 ↗
27. 10.1021/cm061458o10.1021/cm061458o ↗
28. 10.1039/B306780G10.1039/B306780G ↗
29. 10.1016/j.electacta.2011.08.11810.1016/j.electacta.2011.08.118 ↗
30. 10.1103/RevModPhys.76.72510.1103/RevModPhys.76.725 ↗
31. 10.1016/S0370-1573(02)00009-110.1016/S0370-1573(02)00009-1 ↗
32. 10.1063/1.144621510.1063/1.1446215 ↗
33. 10.1007/s12274-013-0381-z10.1007/s12274-013-0381-z ↗
34. Pohl U. W. · 201310.1007/978-3-642-32970-8 ↗
35. 10.1103/PhysRevLett.75.296810.1103/PhysRevLett.75.2968 ↗
36. Wolf D. · 1992
37. 10.1016/S0921-4526(02)00584-710.1016/S0921-4526(02)00584-7 ↗
38. 10.1103/PhysRevLett.27.72710.1103/PhysRevLett.27.727 ↗
39. 10.1063/1.360033310.1063/1.3600333 ↗
40. 10.1063/1.238479810.1063/1.2384798 ↗
41. 10.1021/ar300176y10.1021/ar300176y ↗
42. 10.1016/j.electacta.2010.10.01210.1016/j.electacta.2010.10.012 ↗
43. 10.1016/j.jpowsour.2012.11.15110.1016/j.jpowsour.2012.11.151 ↗
44. 10.1016/j.jpowsour.2011.10.06710.1016/j.jpowsour.2011.10.067 ↗
45. 10.1063/1.274374610.1063/1.2743746 ↗
46. 10.1021/jp308077a10.1021/jp308077a ↗