Tin-Coated Viral Nanoforests as Sodium-Ion Battery Anodes
Source abstract
Abstract
Designed as a high-capacity alloy host for Na-ion chemistry, a forest of Sn nanorods with a unique core-shell structure was synthesized on viral scaffolds, which were genetically engineered to ensure a nearly vertical alignment upon self-assembly onto a metal substrate. The interdigital spaces thus formed between individual rods effectively accommodated the volume expansion and contraction of the alloy upon sodiation/desodiation, while additional carbon-coating engineered over these nanorods further suppressed Sn aggregation during extended electrochemical cycling. Due to the unique nanohierarchy of multiple functional layers, the resultant 3D nanoforest of C/Sn/Ni/TMV1cys, binder-free composite electrode already and evenly assembled on a stainless steel current collector, exhibited supreme capacity utilization and cycling stability toward Na-ion storage and release. An initial capacity of 722 mA·h (g Sn)(-1) along with 405 mA·h (g Sn)(-1) retained after 150 deep cycles demonstrates the longest-cycling nano-Sn anode material for Na-ion batteries reported in the literature to date and marks a significant performance improvement for neat Sn material as alloy host for Na-ion chemistry.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Advancements in Battery Materials · Extraction and Separation Processes · Advanced battery technologies research
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Department of Chemical and Biomolecular Engineering, University of Maryland, College Park, Maryland 20742, United States
Institute for Bioscience and Biotechnology Research and Department of Plant Science and Landscape Architecture, University of Maryland, College Park, Maryland 20742, United States
Electrochemistry Branch, U.S. Army Research Laboratory, Adelphi, Maryland 20783, United States
References (54)
Show source-provided references
1. Palomares V. · Energy Environ. Sci. · 2012 · 5 · 588410.1039/c2ee02781j ↗
2. Ong S. P. · Energy Environ. Sci. · 2011 · 4 · 368010.1039/c1ee01782a ↗
3. Kim S.-W. · Phys. Chem. Chem. Phys. · 2012 · 14 · 329910.1039/c2cp40082k ↗
4. Kim D. · Electrochem. Commun. · 2012 · 18 · 6610.1016/j.elecom.2012.02.020 ↗
5. Ellis B. L. · Nat. Mater. · 2007 · 6 · 74910.1038/nmat2007 ↗
6. Jian Z. · Electrochem. Commun. · 2012 · 14 · 8610.1016/j.elecom.2011.11.009 ↗
7. Cao Y. · Adv. Mater. · 2011 · 23 · 315510.1002/adma.201100904 ↗
8. D’Arienzo M. · Phys. Chem. Chem. Phys. · 2012 · 14 · 594510.1039/c2cp40699c ↗
9. Kitajoua A. · J. Power Sources · 2012 · 198 · 38910.1016/j.jpowsour.2011.09.064 ↗
10. Lee K. T. · Chem. Mater. · 2011 · 23 · 359310.1021/cm200450y ↗
11. Reynauda M. · Solid State Sci. · 2012 · 14 · 1510.1016/j.solidstatesciences.2011.09.004 ↗
12. Sathiya M. · Chem. Mater. · 2012 · 24 · 184610.1021/cm300466b ↗
13. Yabuuchi N. · Nat. Mater. · 2012 · 11 · 51210.1038/nmat3309 ↗
14. Hamani D. · Electrochem. Commun. · 2011 · 13 · 93810.1016/j.elecom.2011.06.005 ↗
15. Wessells C. D. · Nano Lett. · 2011 · 11 · 542110.1021/nl203193q ↗
16. Lu Y. · Chem. Commun. · 2012 · 48 · 654410.1039/c2cc31777j ↗
17. Abouimrane A. · J. Am. Chem. Soc. · 2012 · 134 · 450510.1021/ja211766q ↗
18. Tepavcevic S. · ACS Nano · 2012 · 6 · 53010.1021/nn203869a ↗
19. Alcantara R. · Electrochem. Commun. · 2001 · 3 · 63910.1016/S1388-2481(01)00244-2 ↗
20. Komaba S. · Adv. Funct. Mater. · 2011 · 21 · 385910.1002/adfm.201100854 ↗
21. Wenzel S. · Energy Environ. Sci. · 2011 · 4 · 334210.1039/c1ee01744f ↗
22. Komaba S. · ACS Appl. Mater. Interfaces · 2011 · 3 · 416510.1021/am200973k ↗
23. Cao Y. · Nano Lett. · 2012 · 12 · 378310.1021/nl3016957 ↗
24. Xiong H. · J. Phys. Chem. Lett. · 2011 · 2 · 256010.1021/jz2012066 ↗
25. Sun Q. · Electrochem. Commun. · 2011 · 13 · 146210.1016/j.elecom.2011.09.020 ↗
26. Qian J. · Chem. Commun. · 2012 · 48 · 707010.1039/c2cc32730a ↗
27. Xiao L. · Chem. Commun. · 2012 · 48 · 332110.1039/c2cc17129e ↗
28. Komaba S. · Electrochem. Commun. · 2012 · 21 · 6510.1016/j.elecom.2012.05.017 ↗
29. Chevrier V. L. · J. Electrochem. Soc. · 2011 · 158 · A101110.1149/1.3607983 ↗
30. Xu Y. · Adv. Energy Mater. · 2013 · 3 · 12810.1002/aenm.201200346 ↗
31. Winter M. · Electrochim. Acta · 1999 · 45 · 3110.1016/S0013-4686(99)00191-7 ↗
32. Lee Y. J. · Science · 2009 · 324 · 105110.1126/science.1171541 ↗
33. Liu Y. · Nano Lett. · 2013 · 13 · 29310.1021/nl304104q ↗
34. Royston E. · Langmuir · 2008 · 24 · 90610.1021/la7016424 ↗
35. Lee S. · Nanotechnology · 2005 · 16 · S43510.1088/0957-4484/16/7/019 ↗
36. Chen X. · ACS Nano · 2010 · 4 · 536610.1021/nn100963j ↗
37. Cui L.-F. · Nano Lett. · 2009 · 9 · 49110.1021/nl8036323 ↗
38. Bruce P. G. · Angew. Chem., Int. Ed. · 2008 · 47 · 293010.1002/anie.200702505 ↗
39. Mukaiboa H. · J. Power Sources · 2005 · 146 · 45710.1016/j.jpowsour.2005.03.043 ↗
40. Nishikawa K. · J. Power Sources · 2007 · 174 · 66810.1016/j.jpowsour.2007.06.241 ↗
41. Guo H. · Electrochem. Commun. · 2007 · 9 · 220710.1016/j.elecom.2007.06.021 ↗
42. Ehinon K. K. D. · Chem. Mater. · 2008 · 20 · 538810.1021/cm8006099 ↗
43. Nishikawa K. · J. Power Sources · 2009 · 189 · 72610.1016/j.jpowsour.2008.08.041 ↗
44. Huang L. · Electrochim. Acta · 2009 · 54 · 269310.1016/j.electacta.2008.11.044 ↗
45. Woo S.-W. · Electrochim. Acta · 2010 · 55 · 803010.1016/j.electacta.2010.02.002 ↗
46. Noh M. · Chem. Mater. · 2005 · 17 · 192610.1021/cm0481372 ↗
47. Yu Y. · Angew. Chem., Int. Ed. · 2009 · 48 · 648510.1002/anie.200901723 ↗
48. Derrien G. · Adv. Mater. · 2007 · 19 · 233610.1002/adma.200700748 ↗
49. Fan J. · Adv. Mater. · 2004 · 16 · 143210.1002/adma.200400106 ↗
50. Lee K. T. · J. Am. Chem. Soc. · 2003 · 125 · 565210.1021/ja0345524 ↗
51. Kim C. · J. Raman Spectrosc. · 2004 · 35 · 92810.1002/jrs.1233 ↗
52. Taberna P. L. · Nat. Mater. · 2006 · 5 · 56710.1038/nmat1672 ↗
53. Shaijumon M. M. · Adv. Mater. · 2010 · 22 · 497810.1002/adma.201001922 ↗
54. Wang W. · Nano Lett. · 2012 · 12 · 65510.1021/nl203434g ↗