Engineering Two-Dimensional Mass-Transport Channels of the MoS2 Nanocatalyst toward Improved Hydrogen Evolution Performance
Source abstract
Abstract
In addition to the intrinsic catalytic activity, the mass transport should be taken into adequate account in order to realize the superior performance of electrocatalysts. Here, we engineer the interstitial space between MoS2 nanosheets via the introduction of “spacers” to construct two-dimensional (2D) channels for favorable mass transport. The nano-sized spacers effectively separate MoS2 nanosheets, generating open and connective channels to fulfill timely reactant supply and rapid gas release. Besides, the spacer served as the physical support can prevent the collapse of 2D channels. Because of the engineering of nanostructured channels, a reduction in overpotential by approximately 100 and 360 mV at −10 and −100 mA cm–2, respectively, a decrease in the Tafel slope from 66.7 to 39.4 mV dec–1, and a more stable operation can be achieved. After being integrated by carbon paper, a further improved performance of 198 mV at −200 mA cm–2 and 36 mV dec–1 can be obtained. This work emphasizes the importance of mass-transport channels and paves a way to enhance the hydrogen evolution reaction performance.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Electrocatalysts for Energy Conversion · MXene and MAX Phase Materials · Fuel Cells and Related Materials
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Institute for Regenerative Medicine, Shanghai East Hospital, School of Materials Science and Engineering, Tongji University, Shanghai 200123, China
Key Laboratory of Coal Science and Technology of Ministry of Education and Shanxi Province, Taiyuan University of Technology, Taiyuan 030024 Shanxi, China
Funding
Shanghai Municipal Education Commission · National Natural Science Foundation of China
References (42)
Show source-provided references
1. 10.1021/cr100246c10.1021/cr100246c ↗
2. 10.1021/cr100232610.1021/cr1002326 ↗
3. 10.1002/adma.20130475910.1002/adma.201304759 ↗
4. 10.1126/science.aad499810.1126/science.aad4998 ↗
5. 10.1039/c6cs00328a10.1039/c6cs00328a ↗
6. 10.1039/c4cs00470a10.1039/c4cs00470a ↗
7. 10.1038/nenergy.2017.3110.1038/nenergy.2017.31 ↗
8. 10.1039/c7ta08621k10.1039/c7ta08621k ↗
9. 10.1021/acs.langmuir.7b0069610.1021/acs.langmuir.7b00696 ↗
10. 10.1016/j.pecs.2009.11.00210.1016/j.pecs.2009.11.002 ↗
11. 10.1016/j.ijhydene.2006.01.01810.1016/j.ijhydene.2006.01.018 ↗
12. 10.1016/s0360-3199(02)00027-710.1016/s0360-3199(02)00027-7 ↗
13. 10.1039/c3cc44891f10.1039/c3cc44891f ↗
14. 10.1002/cphc.20110098410.1002/cphc.201100984 ↗
15. 10.1002/adma.20150327010.1002/adma.201503270 ↗
16. 10.1002/adma.20150559710.1002/adma.201505597 ↗
17. 10.1021/acs.chemrev.6b0055810.1021/acs.chemrev.6b00558 ↗
18. 10.1039/c7cs00369b10.1039/c7cs00369b ↗
19. 10.1002/adma.20170571310.1002/adma.201705713 ↗
20. 10.1021/ja207176c10.1021/ja207176c ↗
21. 10.1126/science.123908910.1126/science.1239089 ↗
22. 10.1038/nnano.2015.4010.1038/nnano.2015.40 ↗
23. 10.1021/ja405735d10.1021/ja405735d ↗
24. 10.1021/nn200624910.1021/nn2006249 ↗
25. 10.1002/aenm.20170225410.1002/aenm.201702254 ↗
26. 10.1016/j.jechem.2017.11.00110.1016/j.jechem.2017.11.001 ↗
27. 10.1016/j.jechem.2017.11.02710.1016/j.jechem.2017.11.027 ↗
28. 10.1039/c6tb00296j10.1039/c6tb00296j ↗
29. 10.1016/j.ijhydene.2015.09.07610.1016/j.ijhydene.2015.09.076 ↗
30. 10.1002/anie.20070272110.1002/anie.200702721 ↗
31. 10.1002/adma.20110026110.1002/adma.201100261 ↗
32. 10.1021/ja910307x10.1021/ja910307x ↗
33. 10.1016/j.ijhydene.2013.01.15110.1016/j.ijhydene.2013.01.151 ↗
34. 10.1021/cs300451q10.1021/cs300451q ↗
35. 10.1021/ja408329q10.1021/ja408329q ↗
36. 10.1021/cs400384h10.1021/cs400384h ↗
37. 10.1021/nl202047610.1021/nl2020476 ↗
38. 10.1126/science.114148310.1126/science.1141483 ↗
39. 10.1021/ja201269b10.1021/ja201269b ↗
40. 10.1021/cs500923c10.1021/cs500923c ↗
41. 10.1039/c3cc45416a10.1039/c3cc45416a ↗
42. 10.1038/ncomms761610.1038/ncomms7616 ↗