Large-Scale Synthesis of Metal-Ion-Doped Manganese Dioxide for Enhanced Electrochemical Performance
Source abstract
Abstract
One-dimensional (1D) MnO2 was widely applied in areas of enzyme biosensors, industrial sieves, and energy storage materials owing to its excellent thermal, optical, magnetic, and chemical features. However, its practical application into energy storage devices is often hindered by the bad electronic conductivity (from 10(-5) to 10(-6) S cm(-1)). As is widely known, doping with hetero elements is an efficient way to enhance the electronic conductivity of metal oxides. Herein, a novel and simple molten-salt method is developed to achieve a large-scale preparation of 1D MnO2 nanowires. Such an approach also realizes the easy tuning of electrical properties through doping with different transition metal ions. On the basis of first-principle calculation as well as four-probe measurement, we determined that the conductivity of the doped MnO2 nanowires can be promoted efficiently by utilizing such protocol. Meanwhile, a possible doping route is discussed in detail. As a result, a superior electrochemical performance can be observed in such metal ions (M(+))-doped nanowires. Such high-quality M(+)-doped MnO2 nanowires can satisfy a broad range of application needs beyond the electrochemical capacitors.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Supercapacitor Materials and Fabrication · Advancements in Battery Materials · Conducting polymers and applications
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
College of Chemistry & Molecular Sciences, Wuhan University, Wuhan 430072, People’s Republic of China
Funding
Ministry of Science and Technology of the People's Republic of China
References (38)
Show source-provided references
1. 10.1039/C4EE03229B10.1039/C4EE03229B ↗
2. 10.1021/ja403761s10.1021/ja403761s ↗
3. 10.1039/C4CS00218K10.1039/C4CS00218K ↗
4. 10.1016/j.apcatb.2014.08.04410.1016/j.apcatb.2014.08.044 ↗
5. 10.1039/C4TA03924F10.1039/C4TA03924F ↗
6. 10.1002/anie.20130397110.1002/anie.201303971 ↗
7. 10.1021/es400878c10.1021/es400878c ↗
8. 10.1039/c2jm33368f10.1039/c2jm33368f ↗
9. 10.1039/C0CS00127A10.1039/C0CS00127A ↗
10. 10.1016/j.physb.2011.12.12310.1016/j.physb.2011.12.123 ↗
11. 10.1021/nn101754k10.1021/nn101754k ↗
12. 10.1021/jp810452k10.1021/jp810452k ↗
13. 10.1021/jp804924f10.1021/jp804924f ↗
14. 10.1039/b615972a10.1039/b615972a ↗
15. 10.1021/ja017710510.1021/ja0177105 ↗
16. 10.1039/c3ta11194f10.1039/c3ta11194f ↗
17. 10.1007/s10853-012-6783-610.1007/s10853-012-6783-6 ↗
18. 10.1021/am900094e10.1021/am900094e ↗
19. 10.1039/C4TA05568C10.1039/C4TA05568C ↗
20. 10.1002/ange.20120899310.1002/ange.201208993 ↗
21. 10.1021/nl202663510.1021/nl2026635 ↗
22. 10.1021/am501437510.1021/am5014375 ↗
23. 10.1038/srep0909410.1038/srep09094 ↗
24. 10.1021/jp512795g10.1021/jp512795g ↗
25. 10.1149/1.346786510.1149/1.3467865 ↗
26. 10.1016/j.matlet.2011.03.07410.1016/j.matlet.2011.03.074 ↗
27. 10.1016/j.matchemphys.2011.04.07410.1016/j.matchemphys.2011.04.074 ↗
28. 10.1016/j.electacta.2007.08.05210.1016/j.electacta.2007.08.052 ↗
29. 10.1039/C5RA09278G10.1039/C5RA09278G ↗
30. 10.1021/jp710878510.1021/jp7108785 ↗
31. 10.1021/jp811407q10.1021/jp811407q ↗
32. 10.1021/jp054333010.1021/jp0543330 ↗
33. 10.1016/j.matchemphys.2007.01.00510.1016/j.matchemphys.2007.01.005 ↗
34. 10.1021/nl201382810.1021/nl2013828 ↗
35. 10.1039/c3nr02119j10.1039/c3nr02119j ↗
36. 10.1039/C1JM14804D10.1039/C1JM14804D ↗
37. 10.1021/nl800925j10.1021/nl800925j ↗
38. 10.1149/1.313324710.1149/1.3133247 ↗