journal article·2020-11-23

TiO2 Nanorod Array Conformally Coated with a Monolayer MoS2 Film: An Efficient Electrocatalyst for Hydrogen Evolution Reaction

Anh Duc Nguyen, Thi Hue Pham, Tri Khoa Nguyen, Hamid Ullah, Zeeshan Tahir, Yun Chang Park, Jongwoo Park, Joon Ik Jang, Young Han Shin, Yong Soo Kim

ACS Applied Energy Materials· Volume 3· Issue 11
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Abstract

Heterostructures, particularly the shell–core (2D@1D) nanostructure with atomically thin layers of transition metal dichalcogenides, exhibit an excellent electrocatalytic hydrogen evolution reaction (HER) activity. Herein, we introduce a facile and precisely controlled synthesis of a shell–core heterostructure that comprises TiO2 nanorods (TNRs) as a core array conformally covered by a continuous monolayer molybdenum disulfide (ML-MoS2) film as a shell. The TNR array was grown by a hydrothermal process, followed by the conformal coating of the ML-MoS2 film via metal–organic chemical vapor deposition. Interestingly, the shell–core heterostructure (ML-MoS2@TNRs) shows a significant enhancement in the HER activity with an onset overpotential at 140 mV vs reversible hydrogen electrode and a Tafel slope of ∼80 mV/dec. Based on our experimental results together with first-principle calculations, we attribute the enhanced HER performance of ML-MoS2@TNRs to the synergetic effect of the following characteristics. (i) A large number of active sites owing to TNRs’ high surface to volume ratio. (ii) A considerable reduction in the charge transfer resistance caused by the direct growth of ML-MoS2 over the TNR array, naturally rendering low electrical loss contacts compared to the conventional transfer process. Moreover, the direction of the built-in electric field in the MoS2/TiO2 heterostructure also facilitates the flow of electrons from the electrode to the electrocatalyst surface, consequently decreasing the charge transfer resistance. (iii) The high intrinsic HER activity of the active sites owing to the low Gibbs free energy of the catalytic surface (ML-MoS2@TNRs). Moreover, by virtue of the high crystalline quality of ML-MoS2, the ML-MoS2@TNRs sample shows excellent stability and working durability. Clearly, these characteristics suggest that our proposed method has great potential for practical applications in the form of large-scale HER devices.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Electrocatalysts for Energy Conversion · Advanced Photocatalysis Techniques · Chalcogenide Semiconductor Thin Films

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

Affiliations

Department of Physics and Energy Harvest-Storage Research Center, University of Ulsan, Ulsan 44610, South Korea

Multiscale Materials Modeling Laboratory, Department of Physics, University of Ulsan, Ulsan 44610, South Korea

NTT Hi-Tech Institute, Nguyen Tat Thanh University, Ho Chi Minh City 70000, Viet Nam

Measurement and Analysis Division, National Nanofab Center, Daejeon 34141, South Korea

Department of Physics, Sogang University, Seoul 04107, South Korea

Funding

National Research Foundation of Korea

References (70)

Show source-provided references
1. 10.1021/acsnano.5b0555610.1021/acsnano.5b05556 ↗
2. 10.1002/adma.20150559710.1002/adma.201505597 ↗
3. 10.1038/nnano.2010.27910.1038/nnano.2010.279 ↗
4. 10.1038/nnano.2012.19310.1038/nnano.2012.193 ↗
5. 10.1002/adma.20140462210.1002/adma.201404622 ↗
6. 10.1039/C7TA01457K10.1039/C7TA01457K ↗
7. 10.1021/nn200659w10.1021/nn200659w ↗
8. 10.1021/acsami.7b1585410.1021/acsami.7b15854 ↗
9. 10.1021/ja201269b10.1021/ja201269b ↗
10. 10.1126/science.114148310.1126/science.1141483 ↗
11. 10.1021/acsami.6b1129810.1021/acsami.6b11298 ↗
12. 10.1021/cs500923c10.1021/cs500923c ↗
13. 10.1002/adma.20150327010.1002/adma.201503270 ↗
14. 10.1038/nchem.158910.1038/nchem.1589 ↗
15. 10.1021/ja050469010.1021/ja0504690 ↗
16. 10.1021/nl400258t10.1021/nl400258t ↗
17. 10.1021/acsnano.5b0218810.1021/acsnano.5b02188 ↗
18. 10.1038/nmat343910.1038/nmat3439 ↗
19. 10.1038/ncomms1443010.1038/ncomms14430 ↗
20. 10.1021/acs.nanolett.5b0433110.1021/acs.nanolett.5b04331 ↗
21. 10.1038/nmat456410.1038/nmat4564 ↗
22. 10.1021/nl403620g10.1021/nl403620g ↗
23. 10.1021/ja404523s10.1021/ja404523s ↗
24. 10.1021/ar500202210.1021/ar5002022 ↗
25. 10.1002/adfm.20180329110.1002/adfm.201803291 ↗
26. 10.1002/anie.20181010410.1002/anie.201810104 ↗
27. 10.1021/nl404444k10.1021/nl404444k ↗
28. 10.1021/nl303909f10.1021/nl303909f ↗
29. 10.1021/nl202047610.1021/nl2020476 ↗
30. 10.1021/acsaem.8b0211910.1021/acsaem.8b02119 ↗
31. 10.1002/adma.20150167810.1002/adma.201501678 ↗
32. 10.1021/ja401348510.1021/ja4013485 ↗
33. 10.1039/c2nr31833d10.1039/c2nr31833d ↗
34. 10.1039/c3ta13579a10.1039/c3ta13579a ↗
35. 10.1021/acsnano.9b0260810.1021/acsnano.9b02608 ↗
36. 10.1016/j.materresbull.2020.11093610.1016/j.materresbull.2020.110936 ↗
37. 10.1021/acsomega.7b0034510.1021/acsomega.7b00345 ↗
38. 10.1016/j.electacta.2018.10.15310.1016/j.electacta.2018.10.153 ↗
39. 10.1021/acsnano.6b0631910.1021/acsnano.6b06319 ↗
40. 10.1021/acs.jpcc.8b0395710.1021/acs.jpcc.8b03957 ↗
41. 10.1039/c3nr02994h10.1039/c3nr02994h ↗
42. 10.1039/C4NR02014F10.1039/C4NR02014F ↗
43. 10.1039/C4NR06754A10.1039/C4NR06754A ↗
44. 10.1039/c4nr01528b10.1039/c4nr01528b ↗
45. 10.1039/C8NA00130H10.1039/C8NA00130H ↗
46. 10.1021/ja510442p10.1021/ja510442p ↗
47. 10.1038/srep1873010.1038/srep18730 ↗
48. 10.1021/acscatal.5b0180310.1021/acscatal.5b01803 ↗
49. 10.1038/s41524-019-0161-810.1038/s41524-019-0161-8 ↗
50. 10.1021/acs.chemmater.5b0098610.1021/acs.chemmater.5b00986 ↗
51. 10.1039/C7CP06636H10.1039/C7CP06636H ↗
52. 10.1039/C7CP00636E10.1039/C7CP00636E ↗
53. 10.1088/1361-6641/aa879610.1088/1361-6641/aa8796 ↗
54. 10.1039/C7RA03633G10.1039/C7RA03633G ↗
55. 10.1021/acsomega.9b0320510.1021/acsomega.9b03205 ↗
56. 10.1021/acsami.8b1567310.1021/acsami.8b15673 ↗
57. 10.1039/C7EE03457A10.1039/C7EE03457A ↗
58. 10.1103/PhysRevB.54.1116910.1103/PhysRevB.54.11169 ↗
59. 10.1103/PhysRevB.50.1795310.1103/PhysRevB.50.17953 ↗
60. 10.1103/PhysRevB.59.175810.1103/PhysRevB.59.1758 ↗
61. 10.1103/PhysRevLett.77.386510.1103/PhysRevLett.77.3865 ↗
62. 10.1088/0022-3727/1/7/41610.1088/0022-3727/1/7/416 ↗
63. 10.1103/PhysRevB.84.15541310.1103/PhysRevB.84.155413 ↗
64. 10.1021/acs.jpcc.5b0295010.1021/acs.jpcc.5b02950 ↗
65. 10.1088/1361-6528/aae1e410.1088/1361-6528/aae1e4 ↗
66. 10.1021/ja01623a00410.1021/ja01623a004 ↗
67. 10.1021/ja00246a02110.1021/ja00246a021 ↗
68. 10.1103/PhysRevB.65.22411210.1103/PhysRevB.65.224112 ↗
69. 10.1016/S0167-5729(02)00100-010.1016/S0167-5729(02)00100-0 ↗
70. 10.1007/s10853-010-5113-010.1007/s10853-010-5113-0 ↗