journal article·2018-10-10

Porous MXene Frameworks Support Pyrite Nanodots toward High-Rate Pseudocapacitive Li/Na-Ion Storage

Cheng-Feng Du, Qinghua Liang, Yun Zheng, Yubo Luo, Hui Mao, Qingyu Yan

ACS Applied Materials & Interfaces· Volume 10· Issue 40
Publisher page

Abstract

Presented are the novel Ti3C2Tx MXene-based nanohybrid that decorated by pyrite nanodots on its surface (denoted as FeS2@MXene). The nanohybrid was obtained by the one-step sulfurization of self-assembled iron hydroxide@MXene precursor. When used for Li/Na-ion storage, the FeS2@MXene nanohybrid present excellent rate capabilities. Particularly, for Li-ion storage, an elevated reversible specific capacity of 762 mAh g–1 at 10 A g–1 after 1000 cycles was achieved. And for Na-ion storage, the FeS2@MXene nanohybrid also delivering a reversible specific capacity of 563 mAh g–1 after 100 cycles at a current density of 0.1 A g–1.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: MXene and MAX Phase Materials · Advancements in Battery Materials · Supercapacitor Materials and Fabrication

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

Affiliations

State Key Laboratory of Solidification Processing, Center of Advanced Lubrication and Seal Materials, Northwestern Polytechnical University, Xi’an, Shaanxi 710072, P.R. China

School of Materials Science and Engineering, Nanyang Technological University, 50 Nanyang Avenue, Singapore 639798, Singapore

College of Chemistry and Materials Science, Sichuan Normal University, Chengdu 610068, P.R. China

Funding

Energy Market Authority of Singapore · Ministry of Education - Singapore · National Research Foundation Singapore

References (30)

Show source-provided references
1. 10.1002/anie.20141037610.1002/anie.201410376 ↗
2. 10.1007/s40843-015-0084-810.1007/s40843-015-0084-8 ↗
3. 10.1021/acs.chemrev.7b0068910.1021/acs.chemrev.7b00689 ↗
4. 10.1038/natrevmats.2016.9810.1038/natrevmats.2016.98 ↗
5. 10.1021/acsnano.6b0766810.1021/acsnano.6b07668 ↗
6. 10.1021/acsanm.8b0004510.1021/acsanm.8b00045 ↗
7. 10.1002/aenm.20170248510.1002/aenm.201702485 ↗
8. 10.1021/acs.chemmater.7b0284710.1021/acs.chemmater.7b02847 ↗
9. 10.1016/j.apsusc.2015.11.08910.1016/j.apsusc.2015.11.089 ↗
10. 10.1038/ncomms1390710.1038/ncomms13907 ↗
11. 10.1002/adma.20170236710.1002/adma.201702367 ↗
12. 10.1039/b709167b10.1039/b709167b ↗
13. 10.1016/j.cej.2016.02.09510.1016/j.cej.2016.02.095 ↗
14. 10.1021/ja300823a10.1021/ja300823a ↗
15. 10.1063/1.36917410.1063/1.369174 ↗
16. Murai K. i. · AIP Conf. Proc. · 2007 · 882 · 46310.1063/1.2644559 ↗
17. 10.1002/aenm.20170048210.1002/aenm.201700482 ↗
18. 10.2116/bunsekikagaku.40.11_60910.2116/bunsekikagaku.40.11_609 ↗
19. 10.1039/C4TA00759J10.1039/C4TA00759J ↗
20. 10.1088/0031-8949/1/5-6/02010.1088/0031-8949/1/5-6/020 ↗
21. 10.1021/acsami.7b0057810.1021/acsami.7b00578 ↗
22. 10.1016/j.nanoen.2017.05.01210.1016/j.nanoen.2017.05.012 ↗
23. 10.1149/2.0041606jes10.1149/2.0041606jes ↗
24. 10.1039/C5TA00623F10.1039/C5TA00623F ↗
25. 10.1039/C5CC08002A10.1039/C5CC08002A ↗
26. 10.1002/adma.20170154610.1002/adma.201701546 ↗
27. 10.1002/aenm.20170019310.1002/aenm.201700193 ↗
28. 10.1038/nmat229710.1038/nmat2297 ↗
29. 10.1039/C5TA00988J10.1039/C5TA00988J ↗
30. 10.1039/C5NR06843F10.1039/C5NR06843F ↗