journal article·2017-06-07

Molybdenum–Tungsten Mixed Oxide Deposited into Titanium Dioxide Nanotube Arrays for Ultrahigh Rate Supercapacitors

He Zhou, Xiaopeng Zou, Kaikai Zhang, Peng Sun, Md. Suzaul Islam, Jianyu Gong, Yanrong Zhang, Jiakuan Yang

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Abstract

A novel method involving the fabrication of Mo–W mixed oxide (Mo x W 1– x O 3 ) is proposed to modify the modest reaction kinetics and poor cycling stability of MoO 3 material. By a simple coelectrodeposition method, a series of Mo x W 1– x O 3 oxides is deposited on a TiO 2 nanotube array substrate. Because of the differences between Mo 6+ and W 6+ in nature, there is significant distortion existing in the mixed oxides, leading to their decreased crystallite size and enlarged lattice space, which facilitates ion diffusion in the solid. As results, the mixed oxides show much better balance between specific capacitance and cycling stability than the bare MoO 3 or WO 3 sample, which suffers from either poor cycling stability or low electrochemical activity. Impressively, the optimal Mo–W mixed oxide exhibits a high specific capacitance of 517.4 F g –1 at 1 A g –1, and, moreover, it retains 89.3% of the capacitance even at a high current density of 10 A g –1, demonstrating ultrahigh rate capability. These findings reveal the potential of the Mo–W mixed oxide for constructing advanced ultrahigh power supercapacitors.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Supercapacitor Materials and Fabrication · Advancements in Battery Materials · Transition Metal Oxide Nanomaterials

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

School of Environmental Science and Engineering, Huazhong University of Science and Technology, Luoyu Road 1037#, Wuhan 430074, China

Materials Science and Engineering, Faculty of Engineering, Kyushu University, 744 Motooka, Nishi-ku, Fukuoka 819-0395, Japan

Institute of Energy and Environment, Inner Mongolia University of Science and Technology, Arding Street 7#, Baotou 014010, China

Funding

Ministry of Science and Technology of the People's Republic of China · Huazhong University of Science and Technology

References (64)

Show source-provided references
1. 10.1126/science.115873610.1126/science.1158736 ↗
2. 10.1038/nmat229710.1038/nmat2297 ↗
3. 10.1039/C1CS15060J10.1039/C1CS15060J ↗
4. 10.1016/S0008-6223(00)00183-410.1016/S0008-6223(00)00183-4 ↗
5. 10.1002/adma.20120214610.1002/adma.201202146 ↗
6. 10.1016/j.jpowsour.2010.06.08410.1016/j.jpowsour.2010.06.084 ↗
7. 10.1016/j.nanoen.2014.10.01510.1016/j.nanoen.2014.10.015 ↗
8. 10.1021/nl500255v10.1021/nl500255v ↗
9. 10.1021/ja805730910.1021/ja8057309 ↗
10. 10.1038/nmat261210.1038/nmat2612 ↗
11. 10.1002/smll.20130199110.1002/smll.201301991 ↗
12. 10.1039/C4EE03229B10.1039/C4EE03229B ↗
13. 10.1021/nl301748m10.1021/nl301748m ↗
14. 10.1039/c1ee01399h10.1039/c1ee01399h ↗
15. 10.1002/adma.20110450210.1002/adma.201104502 ↗
16. 10.1039/C4TA04996A10.1039/C4TA04996A ↗
17. 10.1039/C4TA06923D10.1039/C4TA06923D ↗
18. 10.1016/S0167-2738(97)00418-910.1016/S0167-2738(97)00418-9 ↗
19. 10.1149/1.180145110.1149/1.1801451 ↗
20. 10.1126/science.121300310.1126/science.1213003 ↗
21. 10.1021/cm500271u10.1021/cm500271u ↗
22. 10.1002/cphc.20100015810.1002/cphc.201000158 ↗
23. 10.1039/c2ee21294c10.1039/c2ee21294c ↗
24. 10.1016/j.nanoen.2014.04.00710.1016/j.nanoen.2014.04.007 ↗
25. 10.1002/adma.20150131010.1002/adma.201501310 ↗
26. 10.1021/la061299n10.1021/la061299n ↗
27. 10.1021/jp075835b10.1021/jp075835b ↗
28. 10.1016/S0927-0248(02)00267-210.1016/S0927-0248(02)00267-2 ↗
29. 10.1039/B313924G10.1039/B313924G ↗
30. 10.1063/1.155583910.1063/1.1555839 ↗
31. 10.1016/j.jssc.2009.09.02510.1016/j.jssc.2009.09.025 ↗
32. 10.1002/aenm.20120038010.1002/aenm.201200380 ↗
33. 10.1016/j.jpowsour.2014.09.03010.1016/j.jpowsour.2014.09.030 ↗
34. 10.1039/c2ee03158b10.1039/c2ee03158b ↗
35. 10.1021/jp408288310.1021/jp4082883 ↗
36. 10.1021/la047276v10.1021/la047276v ↗
37. 10.1016/0584-8539(94)00247-910.1016/0584-8539(94)00247-9 ↗
38. 10.1016/0022-4596(87)90359-810.1016/0022-4596(87)90359-8 ↗
39. 10.1021/ja011315x10.1021/ja011315x ↗
40. 10.1021/jp501095y10.1021/jp501095y ↗
41. 10.1016/j.electacta.2010.05.00110.1016/j.electacta.2010.05.001 ↗
42. 10.1016/j.jelechem.2009.10.00610.1016/j.jelechem.2009.10.006 ↗
43. 10.3891/acta.chem.scand.04-079310.3891/acta.chem.scand.04-0793 ↗
44. 10.1016/0022-3697(95)00063-110.1016/0022-3697(95)00063-1 ↗
45. 10.1016/0025-5408(87)90035-310.1016/0025-5408(87)90035-3 ↗
46. 10.1016/j.electacta.2016.01.18210.1016/j.electacta.2016.01.182 ↗
47. 10.1021/nl300173j10.1021/nl300173j ↗
48. 10.1021/am302738r10.1021/am302738r ↗
49. 10.1039/c3cc00065f10.1039/c3cc00065f ↗
50. 10.1016/0013-4686(90)85068-X10.1016/0013-4686(90)85068-X ↗
51. 10.1016/0013-4686(94)E0158-K10.1016/0013-4686(94)E0158-K ↗
52. 10.1021/nn305607710.1021/nn3056077 ↗
53. 10.1038/nmat360110.1038/nmat3601 ↗
54. 10.1016/0022-0728(95)03950-L10.1016/0022-0728(95)03950-L ↗
55. 10.1126/science.aab379810.1126/science.aab3798 ↗
56. 10.1021/am504756u10.1021/am504756u ↗
57. 10.1016/j.electacta.2014.09.10010.1016/j.electacta.2014.09.100 ↗
58. 10.1021/ja807106y10.1021/ja807106y ↗
59. 10.1002/adfm20130185110.1002/adfm201301851 ↗
60. 10.1039/c1cc13474d10.1039/c1cc13474d ↗
61. 10.1007/s11581-015-1423-110.1007/s11581-015-1423-1 ↗
62. 10.1021/nl400378j10.1021/nl400378j ↗
63. 10.1021/jp811309410.1021/jp8113094 ↗
64. 10.1039/C2NR33136E10.1039/C2NR33136E ↗