journal article·2021-01-25

In Situ Construction of a Heterostructured Zn–Mo–Ni–O–S Hollow Microflower for High-Performance Hybrid Supercapacitors

Qiqi Shi, Qi Zhang, Ye Yang, Qian Zang, Zhenyu Xiao, Lingbo Zong, Kun-Peng Wang, Lei Wang

ACS Applied Energy Materials· Volume 4· Issue 1
Publisher page

Abstract

The rational design of a multicomponent electrode material with hollow structures grown on the conductive substrate is an effective approach to boost the electrochemical performance of supercapacitors (SCs). However, there is still a challenge in the in situ construction of such unique structures on the conductive substrate. Herein, a heterostructured multicomponent electrode material, a Zn–Mo–Ni–O–S hollow microflower (Zn–Mo–Ni–O–S HMF) in situ grown on a Ni foam (NF), is fabricated by a simple top-down strategy. Based on the ion-exchange and Kirkendall effect, the microflowers are composed of numerous hollow nanosheets, which are covered by uniform ZnS nanoparticles with a robust adherence. Profiting from the structural merits and the synergistic effect of multiple components, the Zn–Mo–Ni–O–S HMF electrode exhibits a high areal capacitance of 4.39 C cm–2 (6.27 F cm–2) at 1 mA cm–2, which is 3.6 times higher than the 0.86 C cm–2 (1.72 F cm–2) of the Zn–Mo–O precursor and 1.7 times higher than the 2.65 C cm–2 (3.79 F cm–2) of Ni3S2/NiMoO4 (Mo–Ni–O–S). The Zn–Mo–Ni–O–S HMF displays an excellent cycling performance (maintaining 87.9% after 3000 cycles). The hybrid supercapacitor device is assembled by the Zn–Mo–Ni–O–S HMF as the positive electrode and active carbon (AC) as the negative electrode. The device delivers a high energy density of 60.8 Wh kg–1 at a power density of 750.2 W kg–1. The synthetic route provides a reference to the in situ construction of a heterostructured multicomponent electrode material for high-energy SCs.
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Research context

OpenAlex topics: Supercapacitor Materials and Fabrication · Advanced battery technologies research · Conducting polymers and applications

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

Affiliations

State Key Laboratory Base of Eco-Chemical Engineering, Taishan Scholar Advantage and Characteristic Discipline Team of Eco Chemical Process and Technology, College of Chemistry and Molecular Engineering, Qingdao University of Science and Technology, Qingdao 266042, China

Funding

Natural Science Foundation of Qingdao · Taishan Scholar Foundation of Shandong Province · National Natural Science Foundation of China

References (55)

Show source-provided references
1. 10.1002/smll.20180029110.1002/smll.201800291 ↗
2. 10.1016/j.cej.2019.12254410.1016/j.cej.2019.122544 ↗
3. 10.1021/acsami.9b2334610.1021/acsami.9b23346 ↗
4. 10.1016/j.cej.2020.12614510.1016/j.cej.2020.126145 ↗
5. 10.1039/C7TA10413H10.1039/C7TA10413H ↗
6. 10.1016/j.cej.2019.12264010.1016/j.cej.2019.122640 ↗
7. 10.1016/j.jallcom.2020.15616410.1016/j.jallcom.2020.156164 ↗
8. 10.1016/j.cej.2020.12641110.1016/j.cej.2020.126411 ↗
9. 10.1016/j.cej.2019.12206310.1016/j.cej.2019.122063 ↗
10. 10.1039/C9NR09083E10.1039/C9NR09083E ↗
11. 10.1002/adfm.20180328710.1002/adfm.201803287 ↗
12. 10.1016/j.cej.2020.12692810.1016/j.cej.2020.126928 ↗
13. 10.1016/j.cej.2019.01.08310.1016/j.cej.2019.01.083 ↗
14. 10.1016/j.cej.2020.12417510.1016/j.cej.2020.124175 ↗
15. 10.1016/j.cej.2020.12482010.1016/j.cej.2020.124820 ↗
16. 10.1016/j.cej.2019.12221110.1016/j.cej.2019.122211 ↗
17. 10.1002/aenm.20170201410.1002/aenm.201702014 ↗
18. 10.1021/acssuschemeng.8b0426510.1021/acssuschemeng.8b04265 ↗
19. 10.1016/j.cej.2018.09.09510.1016/j.cej.2018.09.095 ↗
20. 10.1016/j.cej.2019.02.13810.1016/j.cej.2019.02.138 ↗
21. 10.1002/aenm.20160239110.1002/aenm.201602391 ↗
22. 10.1016/j.ensm.2019.10.02510.1016/j.ensm.2019.10.025 ↗
23. 10.1016/j.cej.2019.01.10710.1016/j.cej.2019.01.107 ↗
24. 10.1021/acsami.9b0297810.1021/acsami.9b02978 ↗
25. 10.1039/C9NR03784E10.1039/C9NR03784E ↗
26. 10.1016/j.jpowsour.2020.22863110.1016/j.jpowsour.2020.228631 ↗
27. 10.1002/chem.20190285910.1002/chem.201902859 ↗
28. 10.1016/j.cej.2017.12.05510.1016/j.cej.2017.12.055 ↗
29. 10.1002/smll.20130222410.1002/smll.201302224 ↗
30. 10.1016/j.cej.2019.12335710.1016/j.cej.2019.123357 ↗
31. 10.1039/C4TA04833D10.1039/C4TA04833D ↗
32. 10.1039/D0TA04483K10.1039/D0TA04483K ↗
33. 10.1039/C7NR03763E10.1039/C7NR03763E ↗
34. 10.1039/C6NR02600A10.1039/C6NR02600A ↗
35. 10.1016/j.jpowsour.2019.22724710.1016/j.jpowsour.2019.227247 ↗
36. 10.1016/j.mtener.2018.12.00210.1016/j.mtener.2018.12.002 ↗
37. 10.1016/j.apsusc.2020.14664110.1016/j.apsusc.2020.146641 ↗
38. 10.1016/j.nanoen.2018.12.06610.1016/j.nanoen.2018.12.066 ↗
39. 10.1039/C9NJ01384A10.1039/C9NJ01384A ↗
40. 10.1016/j.cej.2018.07.16010.1016/j.cej.2018.07.160 ↗
41. 10.1039/C8NR03919D10.1039/C8NR03919D ↗
42. 10.1039/C8TA08212J10.1039/C8TA08212J ↗
43. 10.1016/j.nanoen.2019.01.07110.1016/j.nanoen.2019.01.071 ↗
44. 10.1016/j.cej.2020.12666410.1016/j.cej.2020.126664 ↗
45. 10.1021/acs.inorgchem.0c0176810.1021/acs.inorgchem.0c01768 ↗
46. 10.1039/D0DT02127J10.1039/D0DT02127J ↗
47. 10.1039/c3ee44164d10.1039/c3ee44164d ↗
48. 10.1039/D0DT01430C10.1039/D0DT01430C ↗
49. 10.1016/j.jssc.2018.12.06010.1016/j.jssc.2018.12.060 ↗
50. 10.1039/C9TA09638H10.1039/C9TA09638H ↗
51. 10.1021/acsami.5b0760710.1021/acsami.5b07607 ↗
52. 10.1039/C6TA04022E10.1039/C6TA04022E ↗
53. 10.1016/j.electacta.2019.13506510.1016/j.electacta.2019.135065 ↗
54. 10.1016/j.electacta.2017.10.11610.1016/j.electacta.2017.10.116 ↗
55. 10.1016/j.jpowsour.2020.22829410.1016/j.jpowsour.2020.228294 ↗