journal article·2019-09

Low‐Temperature Reduction Strategy Synthesized Si/Ti3C2 MXene Composite Anodes for High‐Performance Li‐Ion Batteries

Xiaobin Hui, Ruizheng Zhao, Peng Zhang, Caixia Li, Chengxiang Wang, Longwei Yin

Advanced Energy Materials· Volume 9· Issue 33
Publisher page

Abstract

Abstract Silicon is attracting enormous attention due to its theoretical capacity of 4200 mAh g−1 as an anode for Li‐ion batteries (LIBs). It is of fundamental importance and challenge to develop low‐temperature reaction route to controllably synthesize Si/Ti3C2 MXene LIBs anodes. Herein, a novel and efficient strategy integrating in situ orthosilicate hydrolysis and a low‐temperature reduction process to synthesize Si/Ti3C2 MXene composites is reported. The hydrolysis of tetraethyl orthosilicate leads to homogenous nucleation and growth of SiO2 nanoparticles on the surface of Ti3C2 MXene. Subsequently, SiO2 nanoparticles are reduced to Si via a low‐temperature (200 °C) reduction route. Importantly, Ti3C2 MXene not only provides fast transfer channels for Li+ and electrons, but also relieves volume expansion of Si during cycling. Moreover, the characteristics of excellent pseudocapacitive performance and high conductivity of Ti3C2 MXene can synergistically contribute to the enhancement of energy storage performance. As expected, Ti3C2/Si anode exhibits an outstanding specific capacity of 1849 mAh g−1 at 100 mA g−1, even retaining 956 mAh g−1 at 1 A g−1. The low‐temperature synthetic route to Si/Ti3C2 MXene electrodes and involved battery‐capacitive dual‐model energy storage mechanism has potential in the design of novel high‐performance electrodes for energy storage devices.
Source: crossref · Quality: baseline

Research context

OpenAlex topics: MXene and MAX Phase Materials · Advancements in Battery Materials · Graphene research and applications

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

Affiliations

Key Laboratory for Liquid‐Solid Structural Evolution and Processing of Materials Ministry of Education School of Materials Science and Engineering Shandong University Jinan 250061 P. R. China

Funding

National Natural Science Foundation of China · Taishan Scholar Foundation of Shandong Province · China Postdoctoral Science Foundation · Fundamental Research Fund of Shandong University

References (58)

Show source-provided references
1. 10.1021/nl300206e10.1021/nl300206e ↗
2. 10.1002/aenm.20110048510.1002/aenm.201100485 ↗
3. 10.1002/anie.20160814610.1002/anie.201608146 ↗
4. 10.1002/adma.20110256810.1002/adma.201102568 ↗
5. 10.1002/aenm.20140020710.1002/aenm.201400207 ↗
6. 10.1038/s41467-018-05398-910.1038/s41467-018-05398-9 ↗
7. 10.1002/aenm.20130088210.1002/aenm.201300882 ↗
8. 10.1002/smll.20180118910.1002/smll.201801189 ↗
9. 10.1016/j.jpowsour.2017.12.08610.1016/j.jpowsour.2017.12.086 ↗
10. 10.1002/anie.20090628710.1002/anie.200906287 ↗
11. 10.1021/nl803632310.1021/nl8036323 ↗
12. 10.1038/nnano.2012.3510.1038/nnano.2012.35 ↗
13. 10.1021/nn204896n10.1021/nn204896n ↗
14. 10.1016/j.ensm.2018.09.01910.1016/j.ensm.2018.09.019 ↗
15. 10.1039/c0nr00068j10.1039/c0nr00068j ↗
16. 10.1021/cm504404510.1021/cm5044045 ↗
17. 10.1016/j.ensm.2018.09.01010.1016/j.ensm.2018.09.010 ↗
18. 10.1016/j.nanoen.2014.08.02010.1016/j.nanoen.2014.08.020 ↗
19. 10.1039/C3EE43322F10.1039/C3EE43322F ↗
20. 10.1002/adma.20130084410.1002/adma.201300844 ↗
21. 10.1002/adfm.20170523510.1002/adfm.201705235 ↗
22. 10.1039/C7CC05816K10.1039/C7CC05816K ↗
23. 10.1002/aenm.20160148110.1002/aenm.201601481 ↗
24. 10.1038/nenergy.2016.11310.1038/nenergy.2016.113 ↗
25. 10.1002/smll.20180245710.1002/smll.201802457 ↗
26. 10.1002/adma.20130275710.1002/adma.201302757 ↗
27. 10.1002/adma.20170743010.1002/adma.201707430 ↗
28. 10.1016/j.ceramint.2018.03.22310.1016/j.ceramint.2018.03.223 ↗
29. 10.1021/am501144q10.1021/am501144q ↗
30. 10.1021/ja308463r10.1021/ja308463r ↗
31. 10.1021/acsenergylett.7b0106310.1021/acsenergylett.7b01063 ↗
32. 10.1002/aenm.20180208710.1002/aenm.201802087 ↗
33. 10.1016/j.nanoen.2016.10.06210.1016/j.nanoen.2016.10.062 ↗
34. 10.1016/j.nanoen.2017.02.04310.1016/j.nanoen.2017.02.043 ↗
35. 10.1016/j.nanoen.2017.07.02310.1016/j.nanoen.2017.07.023 ↗
36. 10.1002/adfm.20180319610.1002/adfm.201803196 ↗
37. 10.1002/aenm.20180151410.1002/aenm.201801514 ↗
38. 10.1016/j.elecom.2018.10.00310.1016/j.elecom.2018.10.003 ↗
39. 10.1021/acsnano.8b0882110.1021/acsnano.8b08821 ↗
40. 10.1038/s41467-019-08383-y10.1038/s41467-019-08383-y ↗
41. 10.1038/ncomms1571710.1038/ncomms15717 ↗
42. 10.1002/chem.20150442010.1002/chem.201504420 ↗
43. 10.1002/anie.20100163410.1002/anie.201001634 ↗
44. 10.1039/C5EE02487K10.1039/C5EE02487K ↗
45. 10.1002/aelm.20160025510.1002/aelm.201600255 ↗
46. 10.1039/C4NR02080D10.1039/C4NR02080D ↗
47. 10.1038/nature1397010.1038/nature13970 ↗
48. 10.1038/ncomms266410.1038/ncomms2664 ↗
49. 10.1002/adfm.20160571110.1002/adfm.201605711 ↗
50. 10.1021/nl401836c10.1021/nl401836c ↗
51. 10.1016/j.ensm.2018.04.02910.1016/j.ensm.2018.04.029 ↗
52. 10.1002/adma.20170241010.1002/adma.201702410 ↗
53. 10.1039/C7TA08261D10.1039/C7TA08261D ↗
54. 10.1038/s41467-018-04610-010.1038/s41467-018-04610-0 ↗
55. 10.1002/adfm.20160232410.1002/adfm.201602324 ↗
56. 10.1149/1.183857110.1149/1.1838571 ↗
57. 10.1021/jp074464w10.1021/jp074464w ↗
58. 10.1038/nmat261210.1038/nmat2612 ↗