3D-Assembled rutile TiO 2 spheres with c -channels for efficient lithium-ion storage
Source abstract
Abstract
Three-dimensional (3D) TiO2 architectures have attracted significant attention recently as they can improve the electrochemical stability and realize the full potential of TiO2-based anodes in lithium ion batteries. Here, flower-like rutile TiO2 spheres with radially assembled nanorods (c-channels) were fabricated via a simple hydrothermal method. The 3D radial architecture affords massive active sites to fortify the lithium storage. Moreover, the presence of c-channels facilitates electrolyte infiltration and offers facile pathways for efficient Li+ transport. As a result, this flower-like rutile TiO2 anode gives significantly enhanced specific capacities (615 mA h g-1 at 1 C and 386 mA h g-1 at 2 C after 400 cycles) and a superior long-term cyclability (up to 10 000 cycles with a specific capacity of 67 mA h g-1 at 100 C). Kinetic analysis reveals that the enhanced diffusion-controlled and surface capacitive storage leads to the excellent electrochemical behavior. This work not only exhibits the enormous advantages of 3D architectures with c-channels, but also provides access to structural design and crystal phase selection for TiO2-based anode materials.
Source: europepmc · Quality: candidate unverified · Source record ↗
Research context
OpenAlex topics: Advancements in Battery Materials · Supercapacitor Materials and Fabrication · Advanced battery technologies research
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Department of Chemistry
National University of Singapore
Singapore 117543
Singapore
National University of Singapore (Suzhou) Research Institute
Funding
Ministry of Education - Singapore
References (48)
Show source-provided references
1. Albertus · Nat. Energy · 2017 · 3 · 1610.1038/s41560-017-0047-2 ↗
2. Lukatskaya · Nat. Energy · 2017 · 2 · 1710510.1038/nenergy.2017.105 ↗
3. Dou · Chem. Soc. Rev. · 2017 · 46 · 733810.1039/C7CS00418D ↗
4. Liu · Sci. Adv. · 2018 · 4 · eaas982010.1126/sciadv.aas9820 ↗
5. Deng · Energy Environ. Sci. · 2009 · 2 · 81810.1039/b823474d ↗
6. Wagemaker · Acc. Chem. Res. · 2013 · 46 · 120610.1021/ar2001793 ↗
7. Dambournet · Chem. Mater. · 2010 · 22 · 117310.1021/cm902613h ↗
8. Zhu · Energy Environ. Sci. · 2012 · 5 · 665210.1039/c2ee03410g ↗
9. Dawson · J. Phys. Chem. C · 2016 · 120 · 2291010.1021/acs.jpcc.6b08842 ↗
10. Lou · Small · 2019 · 15 · 190474010.1002/smll.201904740 ↗
11. Arico · Nat. Mater. · 2005 · 4 · 36610.1038/nmat1368 ↗
12. Shin · Chem. Mater. · 2012 · 24 · 54310.1021/cm2031009 ↗
13. Myung · Energy Environ. Sci. · 2013 · 6 · 260910.1039/c3ee41960f ↗
14. Moitzheim · Chem. Mater. · 2017 · 29 · 1000710.1021/acs.chemmater.7b03478 ↗
15. Hao · Adv. Energy Mater. · 2020 · 10 · 190310710.1002/aenm.201903107 ↗
16. Hu · Adv. Mater. · 2006 · 18 · 142110.1002/adma.200502723 ↗
17. Wagemaker · J. Am. Chem. Soc. · 2007 · 129 · 432310.1021/ja067733p ↗
18. Bach · Electrochim. Acta · 2010 · 55 · 495210.1016/j.electacta.2010.03.101 ↗
19. Koudriachova · J. Power Sources · 2011 · 196 · 689810.1016/j.jpowsour.2010.12.081 ↗
20. Xu · Chem. Commun. · 2013 · 49 · 897310.1039/c3cc45254a ↗
21. Ni · Adv. Mater. · 2018 · 30 · 170433710.1002/adma.201704337 ↗
22. Sun · J. Am. Chem. Soc. · 2011 · 133 · 1931410.1021/ja208468d ↗
23. Wang · Adv. Mater. · 2012 · 24 · 412410.1002/adma.201104546 ↗
24. Zhang · Angew. Chem., Int. Ed. · 2014 · 53 · 1259010.1002/anie.201406476 ↗
25. Guan · Sci. Adv. · 2016 · 2 · e150155410.1126/sciadv.1501554 ↗
26. Wei · Adv. Funct. Mater. · 2017 · 27 · 170327010.1002/adfm.201703270 ↗
27. Lee · J. Am. Chem. Soc. · 2018 · 140 · 1667610.1021/jacs.8b09487 ↗
28. Lan · J. Am. Chem. Soc. · 2019 · 141 · 1675510.1021/jacs.9b06962 ↗
29. Sushko · J. Phys. Chem. C · 2010 · 114 · 2027710.1021/jp107982c ↗
30. Baek · Chem. Commun. · 2015 · 51 · 1501910.1039/C5CC04864H ↗
31. Hong · Electrochim. Acta · 2016 · 202 · 20310.1016/j.electacta.2016.04.017 ↗
32. Zhang · ChemNanoMat · 2016 · 2 · 76410.1002/cnma.201600093 ↗
33. Lin · Phys. Chem. Chem. Phys. · 2015 · 17 · 720810.1039/C4CP05722H ↗
34. McNulty · Adv. Energy Mater. · 2017 · 7 · 160229110.1002/aenm.201602291 ↗
35. Scanlon · Nat. Mater. · 2013 · 12 · 79810.1038/nmat3697 ↗
36. Ketteler · J. Phys. Chem. C · 2007 · 111 · 827810.1021/jp068606i ↗
37. Li · Nat. Commun. · 2015 · 6 · 588110.1038/ncomms6881 ↗
38. Milne · J. Phys. Chem. C · 2009 · 113 · 1298310.1021/jp8087995 ↗
39. Marinaro · J. Power Sources · 2011 · 196 · 982510.1016/j.jpowsour.2011.07.008 ↗
40. Moitzheim · J. Electrochem. Soc. · 2019 · 166 · A110.1149/2.1091816jes ↗
41. Ai · Adv. Energy Mater. · 2015 · 5 · 150055910.1002/aenm.201500559 ↗
42. Wen · Sci. Rep. · 2015 · 5 · 1180410.1038/srep11804 ↗
43. Hibino · J. Power Sources · 2004 · 126 · 13910.1016/j.jpowsour.2003.08.025 ↗
44. Lee · Adv. Funct. Mater. · 2017 · 27 · 170353810.1002/adfm.201703538 ↗
45. Weppner · J. Electrochem. Soc. · 1977 · 124 · 156910.1149/1.2133112 ↗
46. Wang · J. Phys. Chem. C · 2007 · 111 · 1492510.1021/jp074464w ↗
47. Augustyn · Nat. Mater. · 2013 · 12 · 51810.1038/nmat3601 ↗
48. Chen · Nat. Commun. · 2015 · 6 · 692910.1038/ncomms7929 ↗