journal article·2018-07-18

Self-Assembly-Assisted Facile Synthesis of MoS2-Based Hybrid Tubular Nanostructures for Efficient Bifunctional Electrocatalysis

Chenyang Zhao, Youfang Zhang, Lunfeng Chen, Chaoyi Yan, Peixin Zhang, Jia Ming Ang, Xuehong Lu

ACS Applied Materials & Interfaces· Volume 10· Issue 28
Publisher page

Abstract

In this work, MoS2-based hybrid tubular nanostructures are facilely synthesized via a self-assembly-assisted process and evaluated as a bifunctional electrocatalyst for hydrogen evolution reactions (HERs) and oxygen reduction reactions (ORRs). By simply mixing the reactants under ambient conditions, (NH4)2MoS4/polydopamine (PDA) hybrid nanospheres are formed. The protonated dopamine is linked to tetrahedral [MoS4]2– via weak N–H···S and O–H···S interactions, causing the PDA nanospheres merging together and forming nanorods under stirring-induced shear force. Moreover, the oxidative polymerization of dopamine proceeds on the surface of the nanorods, whereas it is prohibited inside the nanorods owing to lack of oxygen, leading to outward diffusion of dopamine and hence cavitation. After annealing, the tubular morphology is perfectly retained, while ultrafine MoS2 monolayers are formed due to the confinement of the framework. Benefiting from these unique structural features, the MoS2/C hybrid nanotubes possess abundant active sites and high surface area, as well as boost electronic and ionic transport, remarkably enhancing their electrocatalytic activities. The onset and half-wave potentials are 0.91 and 0.82 V, respectively, for ORR, close to those of Pt/C. Moreover, low onset potential and small Tafel slope are also observed for HER, demonstrating the potential of the hybrid nanotubes as a promising non-noble metal bifunctional electrocatalyst.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Electrocatalysts for Energy Conversion · MXene and MAX Phase Materials · Advanced Photocatalysis Techniques

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

Affiliations

College of Chemistry and Environmental Engineering, Shenzhen University, 1066 Xueyuan Avenue, Nanshan District, Shenzhen 518071, PR China

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

Funding

Natural Science Foundation, Shenzhen University

References (48)

Show source-provided references
1. 10.1002/aenm.20160206810.1002/aenm.201602068 ↗
2. 10.1021/acsami.7b0623110.1021/acsami.7b06231 ↗
3. 10.1021/acsami.7b1174810.1021/acsami.7b11748 ↗
4. 10.1002/ange.20150434910.1002/ange.201504349 ↗
5. 10.1002/anie.20170810510.1002/anie.201708105 ↗
6. 10.1039/c1jm12492g10.1039/c1jm12492g ↗
7. 10.1039/c4ta06265e10.1039/c4ta06265e ↗
8. 10.1039/c7nr05825j10.1039/c7nr05825j ↗
9. 10.1021/jz501684510.1021/jz5016845 ↗
10. 10.1002/smll.20070038210.1002/smll.200700382 ↗
11. 10.1002/smll.20160141310.1002/smll.201601413 ↗
12. 10.1021/am509096x10.1021/am509096x ↗
13. 10.1021/am405808810.1021/am4058088 ↗
14. 10.1021/acsami.5b1149210.1021/acsami.5b11492 ↗
15. 10.1039/c5cc01841b10.1039/c5cc01841b ↗
16. 10.1021/acssuschemeng.5b0070010.1021/acssuschemeng.5b00700 ↗
17. 10.1039/c6nr04073j10.1039/c6nr04073j ↗
18. 10.1016/j.carbon.2017.02.01010.1016/j.carbon.2017.02.010 ↗
19. 10.1038/ncomms1443010.1038/ncomms14430 ↗
20. 10.1126/science.267.5195.22210.1126/science.267.5195.222 ↗
21. 10.1021/ja001607i10.1021/ja001607i ↗
22. 10.1002/1521-4095(200102)13:4<283::aid-adma283>3.0.co;2-h10.1002/1521-4095(200102)13:4<283::aid-adma283>3.0.co;2-h ↗
23. 10.1021/jp101298g10.1021/jp101298g ↗
24. 10.1002/ange.20130348010.1002/ange.201303480 ↗
25. 10.1039/c4ee02211d10.1039/c4ee02211d ↗
26. 10.1039/c3cc49647c10.1039/c3cc49647c ↗
27. 10.1039/c4nr06366j10.1039/c4nr06366j ↗
28. 10.1002/adma.20120392310.1002/adma.201203923 ↗
29. 10.1039/c2cc35284b10.1039/c2cc35284b ↗
30. 10.1002/aenm.20170019310.1002/aenm.201700193 ↗
31. 10.1155/2012/93076310.1155/2012/930763 ↗
32. 10.1002/aenm.20130138010.1002/aenm.201301380 ↗
33. 10.1002/aenm.20150111510.1002/aenm.201501115 ↗
34. 10.1002/adma.20140462210.1002/adma.201404622 ↗
35. 10.1002/ange.20151049510.1002/ange.201510495 ↗
36. 10.1039/c3ee43463j10.1039/c3ee43463j ↗
37. 10.1016/j.poly.2007.08.02310.1016/j.poly.2007.08.023 ↗
38. 10.1107/s160053680602241010.1107/s1600536806022410 ↗
39. 10.1002/adfm.20120115610.1002/adfm.201201156 ↗
40. 10.1002/adma.20140200010.1002/adma.201402000 ↗
41. 10.1039/c5ta01600b10.1039/c5ta01600b ↗
42. 10.1039/c5nr06028a10.1039/c5nr06028a ↗
43. 10.1021/acs.langmuir.6b0233110.1021/acs.langmuir.6b02331 ↗
44. 10.1021/acsami.6b1181110.1021/acsami.6b11811 ↗
45. 10.1021/ja408329q10.1021/ja408329q ↗
46. 10.1021/acsami.6b0603110.1021/acsami.6b06031 ↗
47. 10.1002/adma.20130268510.1002/adma.201302685 ↗
48. 10.1039/c5ee00751h10.1039/c5ee00751h ↗