journal article·2018-12-19

Molecular-Level CuS@S Hybrid Nanosheets Constructed by Mineral Chemistry for Energy Storage Systems

Sijie Li, Peng Ge, Feng Jiang, Christopher W. Foster, Craig E. Banks, Wei Xu, Yu Zhang, Wanwan Hong, Chenyang Zhang, Wei Sun, Jiugang Hu, Hongshuai Hou, Yuehua Hu, Xiaobo Ji

ACS Applied Materials & Interfaces· Volume 10· Issue 50
Publisher page

Abstract

The transition-metal sulfide, CuS, is deemed a promising material for energy storage, mainly derived from its good chemisorption and conductivity, although serious capacity fading limits its advancement within reversible lithium storage. Learning from the gold extraction method utilizing the lime-sulfur-synthetic-solution, a CuS@S hybrid utilizing CaSx as both sulfur resource and reductant–oxidant is prepared, which is an efficient approach to apply the metallurgy for the preparation of electrode materials. Regulating the amount of CuCl2, the CuS@S is induced to reach a molecular-level hybrid. When utilized as an anode within a lithium-ion battery, it presents the specific capacity of 514.4 mA h g–1 at 0.1 A g–1 over 200 cycles. Supported by the analyses of pseudo-capacitive behaviors, it is confirmed that the CuS matrix with the suitable content of auxiliary sulfur could improve the durability of the CuS-based anode. Expanding the wider application within lithium–sulfur batteries, the synchronous growth of CuS@S exhibits stronger chemisorption with polysulfides than the mechanical mixture of CuS and S. A suite of in situ electrochemical impedance spectroscopy studies further investigates the stable resistances of the CuS@S within the charge/discharge process, corresponding to the reversible structure evolution. This systematic work may provide a practical fabricating route of metal sulfides for scalable energy storage applications.
Source: openalex_inverted_index · 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

Faculty of Science and Engineering, Manchester Metropolitan University, Manchester M1 5GD, U.K.

Funding

Ministry of Education of the People's Republic of China · Central South University · Hunan Provincial Science and Technology Department · Natural Science Foundation of?Hunan Province · Ministry of Science and Technology of the People's Republic of China · China Association for Science and Technology · China Postdoctoral Science Foundation · Ministry of Human Resources and Social Security · National Natural Science Foundation of China · Postgraduate Electronic Design Competition of China · National Mittal Student Innovation Program

References (54)

Show source-provided references
1. 10.1002/adma.20160175910.1002/adma.201601759 ↗
2. 10.1039/c4ta04980b10.1039/c4ta04980b ↗
3. 10.1002/adma.20170060610.1002/adma.201700606 ↗
4. 10.1039/c3ee42591f10.1039/c3ee42591f ↗
5. 10.1016/j.nanoen.2018.04.01810.1016/j.nanoen.2018.04.018 ↗
6. 10.1021/acsami.7b1857110.1021/acsami.7b18571 ↗
7. 10.1038/srep0925410.1038/srep09254 ↗
8. 10.1038/ncomms968910.1038/ncomms9689 ↗
9. 10.1016/j.ssi.2008.09.00710.1016/j.ssi.2008.09.007 ↗
10. 10.1002/aenm.20170159210.1002/aenm.201701592 ↗
11. 10.1016/j.apsusc.2017.01.14810.1016/j.apsusc.2017.01.148 ↗
12. 10.1016/j.jpowsour.2015.12.04810.1016/j.jpowsour.2015.12.048 ↗
13. 10.1021/acsami.6b1036610.1021/acsami.6b10366 ↗
14. 10.1039/c6ra11990e10.1039/c6ra11990e ↗
15. 10.1016/j.jpowsour.2014.07.00610.1016/j.jpowsour.2014.07.006 ↗
16. 10.1149/2.0871707jes10.1149/2.0871707jes ↗
17. 10.1016/j.cej.2016.05.06810.1016/j.cej.2016.05.068 ↗
18. 10.1016/j.powtec.2011.04.02810.1016/j.powtec.2011.04.028 ↗
19. 10.1016/j.ensm.2018.02.01210.1016/j.ensm.2018.02.012 ↗
20. 10.1016/j.jpcs.2008.11.00910.1016/j.jpcs.2008.11.009 ↗
21. 10.1016/j.matlet.2007.11.06910.1016/j.matlet.2007.11.069 ↗
22. 10.1016/j.jpowsour.2014.01.12410.1016/j.jpowsour.2014.01.124 ↗
23. 10.1021/cm035238b10.1021/cm035238b ↗
24. 10.1016/j.matchemphys.2004.10.04510.1016/j.matchemphys.2004.10.045 ↗
25. 10.1016/j.ensm.2017.01.00210.1016/j.ensm.2017.01.002 ↗
26. 10.1038/ncomms129310.1038/ncomms1293 ↗
27. 10.1002/smll.20140235410.1002/smll.201402354 ↗
28. 10.1002/aenm.20150163610.1002/aenm.201501636 ↗
29. 10.1039/c6ra22434b10.1039/c6ra22434b ↗
30. 10.1021/acsami.6b0947910.1021/acsami.6b09479 ↗
31. 10.1039/c3ee00072a10.1039/c3ee00072a ↗
32. 10.1021/nn404439r10.1021/nn404439r ↗
33. 10.1016/j.nanoen.2017.09.01810.1016/j.nanoen.2017.09.018 ↗
34. 10.1016/j.nanoen.2016.12.01010.1016/j.nanoen.2016.12.010 ↗
35. 10.1016/j.electacta.2012.12.07710.1016/j.electacta.2012.12.077 ↗
36. 10.1021/nl304795g10.1021/nl304795g ↗
37. 10.1021/nl401886810.1021/nl4018868 ↗
38. 10.1149/2.1021514jes10.1149/2.1021514jes ↗
39. 10.1016/j.jpcs.2014.06.01010.1016/j.jpcs.2014.06.010 ↗
40. 10.1021/j100858a03110.1021/j100858a031 ↗
41. 10.1016/j.cej.2017.09.07010.1016/j.cej.2017.09.070 ↗
42. 10.1021/jz501352e10.1021/jz501352e ↗
43. 10.1016/j.colcom.2016.11.00110.1016/j.colcom.2016.11.001 ↗
44. 10.1002/smll.20160063310.1002/smll.201600633 ↗
45. 10.1002/aenm.20170315910.1002/aenm.201703159 ↗
46. 10.1021/acsnano.6b0556610.1021/acsnano.6b05566 ↗
47. 10.1021/acsnano.7b0713210.1021/acsnano.7b07132 ↗
48. 10.1016/j.nanoen.2016.10.05910.1016/j.nanoen.2016.10.059 ↗
49. 10.1016/j.nanoen.2017.07.03810.1016/j.nanoen.2017.07.038 ↗
50. 10.1021/nn403674z10.1021/nn403674z ↗
51. 10.1021/nl404637q10.1021/nl404637q ↗
52. 10.1021/nn403674z10.1021/nn403674z ↗
53. 10.1021/acsami.7b1088610.1021/acsami.7b10886 ↗
54. 10.1002/advs.20180008010.1002/advs.201800080 ↗