Facile Method To Synthesize Na-Enriched Na1+xFeFe(CN)6 Frameworks as Cathode with Superior Electrochemical Performance for Sodium-Ion Batteries
Source abstract
Abstract
Different Na-enriched Na 1+ x FeFe(CN) 6 samples can be synthesized by a facile one-step method, utilizing Na 4 Fe(CN) 6 as the precursor in a different concentration of NaCl solution. As-prepared samples were characterized by a combination of synchrotron X-ray powder diffraction (S-XRD), Mössbauer spectroscopy, Raman spectroscopy, magnetic measurements, thermogravimetric analysis, X-ray photoelectron spectroscopy, and inductively coupled plasma analysis. The electrochemical results show that the Na 1.56 Fe[Fe(CN) 6 ]·3.1H 2 O (PB-5) sample shows a high specific capacity of more than 100 mAh g –1 and excellent capacity retention of 97% over 400 cycles. The details structural evolution during Na-ion insertion/extraction processes were also investigated via in situ synchrotron XRD. Phase transition can be observed during the initial charge and discharge process. The simple synthesis method, superior cycling stability, and cost-effectiveness make the Na-enriched Na 1+ x Fe[Fe(CN) 6 ] a promising cathode for sodium-ion batteries.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Advancements in Battery Materials · Advanced Battery Materials and Technologies · MXene and MAX Phase Materials
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Institute for Superconducting and Electronic Materials, University of Wollongong, Wollongong, New South Wales 2522, Australia
Department of Energy and Materials Engineering, Dongguk University-Seoul, Seoul 100-715, Republic of Korea
Institute of Advanced Materials for Nano-Bio Applications, School of Ophthalmology & Optometry, Wenzhou Medical University, Wenzhou, Zhejiang 325027, China
Australian Synchrotron, 800 Blackburn Road, Clayton, Victoria 3168, Australia
Funding
AutoCRC Ltd · Australian Research Council
References (26)
Show source-provided references
1. Yang Z. G. · Chem. Rev. · 2011 · 111 · 357710.1021/cr100290v ↗
2. Palomares V. · Energy Environ. Sci. · 2012 · 5 · 588410.1039/c2ee02781j ↗
3. Ong S. P. · Energy Environ. Sci. · 2011 · 4 · 368010.1039/c1ee01782a ↗
4. Berthelot R. · Nat. Mater. · 2011 · 10 · 7410.1038/nmat2920 ↗
5. Yabuuchi N. · Nat. Mater. · 2012 · 11 · 51210.1038/nmat3309 ↗
6. Buchholz D. · Chem. Mater. · 2013 · 25 · 14210.1021/cm3029615 ↗
7. Zhang B. · Chem. Commun. · 2014 · 50 · 120910.1039/C3CC48382G ↗
8. Qu Q. T. · J. Power Sources · 2009 · 194 · 122210.1016/j.jpowsour.2009.06.068 ↗
9. Ellis B. L. · Nat. Mater. · 2007 · 6 · 74910.1038/nmat2007 ↗
10. Liu Y. L. · Nano Lett. · 2012 · 12 · 566410.1021/nl302819f ↗
11. Jian Z. L. · Adv. Energy Mater. · 2013 · 3 · 15610.1002/aenm.201200558 ↗
12. Kim H. · J. Am. Chem. Soc. · 2012 · 134 · 1036910.1021/ja3038646 ↗
13. Nishijima M. · J. Power Sources · 2009 · 190 · 55810.1016/j.jpowsour.2009.01.051 ↗
14. Wessells C. D. · Nano Lett. · 2011 · 11 · 542110.1021/nl203193q ↗
15. Lu Y. H. · Chem. Commun. · 2012 · 48 · 654410.1039/c2cc31777j ↗
16. Wang L. · Angew. Chem., Int. Ed. · 2013 · 52 · 196410.1002/anie.201206854 ↗
17. Matsuda T. · Chem. Commun. · 2013 · 49 · 275010.1039/c3cc38839e ↗
18. Wu X. · J. Mater. Chem. A · 2013 · 1 · 1013010.1039/c3ta12036h ↗
19. Qian J. · Adv. Energy Mater. · 2012 · 2 · 41010.1002/aenm.201100655 ↗
20. Yu S. H. · ECS Electrochem. Lett. · 2013 · 2 · A3910.1149/2.008304eel ↗
21. Asakura D. · J. Phys. Chem. C · 2012 · 116 · 836410.1021/jp2118949 ↗
22. You Y. · Energy Environ. Sci. · 2014 · 7 · 164310.1039/C3EE44004D ↗
23. Toby B. H. · J. Appl. Crystallogr. · 2013 · 46 · 54410.1107/S0021889813003531 ↗
24. Vertelman E. J. M. · Chem. Mater. · 2008 · 20 · 123610.1021/cm7032965 ↗
25. Samain L. · J. Phys. Chem. C · 2013 · 117 · 969310.1021/jp3111327 ↗
26. Liu H. · Science · 2014 · 344 · 125281710.1126/science.1252817 ↗