journal article·2019-08

Unlocking Few‐Layered Ternary Chalcogenides for High‐Performance Potassium‐Ion Storage

Huajun Tian, Xuechao Yu, Hezhu Shao, Liubing Dong, Yi Chen, Xiaqin Fang, Chengyin Wang, Weiqiang Han, Guoxiu Wang

Advanced Energy Materials· Volume 9· Issue 29
Publisher page

Abstract

Abstract Potassium‐ion batteries (KIBs) have attracted increasing attention for grid‐scale energy storage due to the abundance of potassium resources, low cost, and competitive energy density. The key challenge for KIBs is to develop high‐performance electrode materials. However, the exploration of high‐capacity and ultrastable electrodes for KIBs remains challenging because of the sluggish diffusion kinetics of K+ ions during the charging/discharging processes. This study reports for the first time a facile ion‐intercalation‐mediated exfoliation method with Mg2+ cations and NO3– anions as ion assistants for the fabrication of expanded few‐layered ternary Ta2NiSe5 (EF‐TNS) flakes with interlayer spacing up to 1.1 nm and abundant Se sites (NiSe4 tetrahedra/TaSe6 octahedra clusters) for superior potassium‐ion storage. The EF‐TNS deliver a high capacity of 315 mAh g–1, excellent rate capability (121 mAh g–1 at a current density of 1000 mA g–1), and ultrastable cycling performance (81.4% capacity retention after 1100 cycles). Detailed theoretical analysis via first‐principles calculations and experimental results elucidate that K+ ions intercalate through the expanded interlayers effectively and prefer to transport along zigzag pathways in layered Ta2NiSe5. This work provides a new avenue for designing novel ternary intercalation/pseudocapacitance‐type KIBs with high capacity, excellent rate capability, and superior long‐term cycling performance.
Source: crossref · Quality: baseline

Research context

OpenAlex topics: Advancements in Battery Materials · Supercapacitor Materials and Fabrication · Advanced Battery Materials and Technologies

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

Affiliations

Centre for Clean Energy Technology University of Technology Sydney Broadway Sydney NSW 2007 Australia

Centre for OptoElectronics and Biophotonics School of Electrical and Electronic Engineering Nanyang Technological University 639798 Singapore Singapore

Ningbo Institute of Materials Technology and Engineering Chinese Academy of Sciences Ningbo 315201 China

School of Chemistry and Chemical Engineering Yangzhou University Yangzhou 225002 China

School of Materials Science and Engineering Zhejiang University Hangzhou 310027 China

Funding

Australian Research Council · National Natural Science Foundation of China · Natural Science Foundation of Jiangsu Province

References (47)

Show source-provided references
1. 10.1038/nchem.158910.1038/nchem.1589 ↗
2. 10.1038/nnano.2015.4010.1038/nnano.2015.40 ↗
3. 10.1038/s41467-018-07710-z10.1038/s41467-018-07710-z ↗
4. 10.1039/C4CS00182F10.1039/C4CS00182F ↗
5. 10.1002/adma.20130496410.1002/adma.201304964 ↗
6. 10.1002/anie.20170642610.1002/anie.201706426 ↗
7. 10.1002/anie.20150993310.1002/anie.201509933 ↗
8. 10.1021/acs.nanolett.7b0524610.1021/acs.nanolett.7b05246 ↗
9. 10.1016/j.joule.2018.01.01010.1016/j.joule.2018.01.010 ↗
10. 10.1016/j.chempr.2018.10.00410.1016/j.chempr.2018.10.004 ↗
11. 10.1038/s41467-018-05786-110.1038/s41467-018-05786-1 ↗
12. 10.1016/j.ensm.2017.12.01810.1016/j.ensm.2017.12.018 ↗
13. 10.1021/acsenergylett.7b0052910.1021/acsenergylett.7b00529 ↗
14. 10.1016/j.ensm.2018.09.01410.1016/j.ensm.2018.09.014 ↗
15. 10.1002/adma.20180003610.1002/adma.201800036 ↗
16. 10.1016/j.nanoen.2018.01.00110.1016/j.nanoen.2018.01.001 ↗
17. 10.1002/adfm.20170612510.1002/adfm.201706125 ↗
18. 10.1002/adfm.20180340910.1002/adfm.201803409 ↗
19. 10.1002/adma.20170206110.1002/adma.201702061 ↗
20. 10.1002/aenm.20180147710.1002/aenm.201801477 ↗
21. 10.1002/adma.20180181210.1002/adma.201801812 ↗
22. 10.1002/adma.20180274510.1002/adma.201802745 ↗
23. 10.1002/adma.20180437810.1002/adma.201804378 ↗
24. 10.1038/ncomms1440810.1038/ncomms14408 ↗
25. 10.1002/adma.20180198410.1002/adma.201801984 ↗
26. 10.1002/adfm.20160380410.1002/adfm.201603804 ↗
27. 10.1103/PhysRevB.87.03512110.1103/PhysRevB.87.035121 ↗
28. 10.1103/PhysRevLett.120.24760210.1103/PhysRevLett.120.247602 ↗
29. 10.1103/PhysRev.158.46210.1103/PhysRev.158.462 ↗
30. 10.1103/PhysRevLett.103.02640210.1103/PhysRevLett.103.026402 ↗
31. 10.1039/C8TA12497C10.1039/C8TA12497C ↗
32. 10.1002/aenm.20170164810.1002/aenm.201701648 ↗
33. 10.1021/acsnano.6b0479610.1021/acsnano.6b04796 ↗
34. 10.1038/nmat261210.1038/nmat2612 ↗
35. 10.1038/ncomms1212210.1038/ncomms12122 ↗
36. 10.1002/adfm.20180369010.1002/adfm.201803690 ↗
37. 10.1016/j.jpowsour.2016.03.06410.1016/j.jpowsour.2016.03.064 ↗
38. 10.1002/adma.20180548610.1002/adma.201805486 ↗
39. 10.1038/am.2014.9810.1038/am.2014.98 ↗
40. 10.1002/adma.20180003610.1002/adma.201800036 ↗
41. 10.1016/j.apmt.2018.10.00410.1016/j.apmt.2018.10.004 ↗
42. 10.1016/j.nanoen.2018.12.08410.1016/j.nanoen.2018.12.084 ↗
43. 10.1103/PhysRevB.47.55810.1103/PhysRevB.47.558 ↗
44. 10.1103/PhysRevB.54.1116910.1103/PhysRevB.54.11169 ↗
45. 10.1103/PhysRevLett.77.386510.1103/PhysRevLett.77.3865 ↗
46. 10.1063/1.338234410.1063/1.3382344 ↗
47. 10.1063/1.132967210.1063/1.1329672 ↗