journal article·2020-07-29

A Universal Process: Self-Templated and Orientated Fabrication of XMoO4 (X: Ni, Co, or Fe) Nanosheets on MoO2 Nanoplates as Electrocatalysts for Efficient Water Splitting

Linjing Yang, Hui Liu, Ziqian Zhou, Yuke Chen, Guowei Xiong, Lili Zeng, Yunqie Deng, Xiaoli Zhang, Hong Liu, Weijia Zhou

ACS Applied Materials & Interfaces· Volume 12· Issue 30
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Abstract

Fabrication of superior nonprecious electrocatalysts is essential for water electrolysis. Herein, the epitaxial growth of the XMoO4 (X = Ni, Co, Fe) nanosheets on the hexagonal MoO2 nanoplates are carried out. The preoxidation of MoO2 nanoplate is fatal to the epitaxial growth of a nanosheets array on MoO2 nanoplates. The hierarchical heterostructure of the vertically aligned NiMo nanosheets on MoO2 nanoplate (NiMo/MoO2) is well-maintained in the process of in situ topotactic reduction transformation from NiMoO4·xH2O/MoO2. Attributing it to the rich electroactive sites from nanosheets array, together with the intrinsic electrocatalytic performance of NiMo alloy, the as-engineered NiMo/MoO2 as electrocatalyst exhibits admirable hydrogen evolution reaction (HER) activity with a small onset potential of −12 mV vs RHE (1 mA cm–2) and a tafel value of 43.6 mV dec–1 at alkaline media. Furthermore, the obtained CoMoO4/MoO2 possesses excellent oxygen evolution performance, which is verified by an ultralow overpotential of 230 mV@10 mA cm–2, small Tafel slope (51 mV dec–1), and robust durability. The developed NiMo/MoO2 and CoMoO4/MoO2 electrocatalysts are assembled into an alkaline electrolyzer, which affords a cell potential of 1.51 V at 10 mA cm–2, as well as outstanding operational durability, which is superior to the typically constructed 20 wt % Pt/C-RuO2 system (1.59 V at 10 mA cm–2). Hence, the universal strategy using MoO2 nanoplates as Mo source and epitaxial substrate may be extended to explore and construct economical and superior Mo-based electrocatalysts for water electrolysis.
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Research context

OpenAlex topics: Electrocatalysts for Energy Conversion · Advanced battery technologies research · Advanced Photocatalysis Techniques

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

Affiliations

Guangzhou Key Laboratory for Surface Chemistry of Energy Materials, New Energy Research Institute, School of Environment and Energy, South China University of Technology, Guangzhou Higher Education Mega Center, Guangzhou, Guangdong 510006, People’s Republic of China

Shandong Collaborative Innovation Center of Technology and Equipements for Biological Diagnosis and Therapy, Institute for Advanced Interdisciplinary Research (iAIR), University of Jinan, Jinan 250022, People’s Republic of China

School of Materials Science and Engineering, Zhengzhou University, Zhengzhou 450001, People’s Republic of China

State Key Laboratory of Crystal Materials, Shandong University, Jinan 250100, People’s Republic of China

Funding

Tip-top Scientific and Technical Innovative Youth Talents of Guangdong Special Support Program · National Natural Science Foundation of China · Natural Science Foundation of Guangdong Province · South China University of Technology

References (53)

Show source-provided references
1. 10.1038/s41467-018-04358-710.1038/s41467-018-04358-7 ↗
2. 10.1021/jacs.5b1275810.1021/jacs.5b12758 ↗
3. 10.1016/j.nanoen.2016.08.02710.1016/j.nanoen.2016.08.027 ↗
4. 10.1038/ncomms906410.1038/ncomms9064 ↗
5. 10.1002/smtd.20190021010.1002/smtd.201900210 ↗
6. 10.1021/acsami.0c0483810.1021/acsami.0c04838 ↗
7. 10.1021/acs.nanolett.7b0103010.1021/acs.nanolett.7b01030 ↗
8. 10.1002/adma.20170238510.1002/adma.201702385 ↗
9. 10.1021/acsnano.7b0660710.1021/acsnano.7b06607 ↗
10. 10.1002/aenm.20170002010.1002/aenm.201700020 ↗
11. 10.1002/adma.20170158910.1002/adma.201701589 ↗
12. 10.1021/jacs.7b1296810.1021/jacs.7b12968 ↗
13. 10.1021/acsenergylett.7b0069110.1021/acsenergylett.7b00691 ↗
14. 10.1016/j.nanoen.2020.10462110.1016/j.nanoen.2020.104621 ↗
15. 10.1021/acsami.0c0053410.1021/acsami.0c00534 ↗
16. 10.1016/j.nanoen.2020.10485010.1016/j.nanoen.2020.104850 ↗
17. 10.1002/anie.20161176710.1002/anie.201611767 ↗
18. 10.1021/acscatal.9b0109310.1021/acscatal.9b01093 ↗
19. 10.1016/j.cclet.2018.10.02610.1016/j.cclet.2018.10.026 ↗
20. 10.1002/anie.20171254910.1002/anie.201712549 ↗
21. 10.1002/aenm.20190042910.1002/aenm.201900429 ↗
22. 10.1002/anie.20181254510.1002/anie.201812545 ↗
23. 10.1016/j.nanoen.2017.05.01110.1016/j.nanoen.2017.05.011 ↗
24. 10.1021/acssuschemeng.6b0187910.1021/acssuschemeng.6b01879 ↗
25. 10.1021/ja510442p10.1021/ja510442p ↗
26. 10.1002/admi.20187006310.1002/admi.201870063 ↗
27. 10.1038/ncomms1543710.1038/ncomms15437 ↗
28. 10.1021/ja410196810.1021/ja4101968 ↗
29. 10.1002/anie.20150961610.1002/anie.201509616 ↗
30. 10.1038/nature1645510.1038/nature16455 ↗
31. 10.1002/anie.20080224810.1002/anie.200802248 ↗
32. 10.1002/adma.20110414510.1002/adma.201104145 ↗
33. 10.1038/nchem.247310.1038/nchem.2473 ↗
34. 10.1016/j.nanoen.2019.05.01310.1016/j.nanoen.2019.05.013 ↗
35. 10.1016/j.nanoen.2019.05.03610.1016/j.nanoen.2019.05.036 ↗
36. 10.1002/adma.20170331110.1002/adma.201703311 ↗
37. 10.1016/j.apcatb.2020.11895610.1016/j.apcatb.2020.118956 ↗
38. 10.1016/j.nanoen.2019.02.02810.1016/j.nanoen.2019.02.028 ↗
39. 10.1016/j.apcatb.2019.02.06210.1016/j.apcatb.2019.02.062 ↗
40. 10.1021/acscatal.8b0481710.1021/acscatal.8b04817 ↗
41. 10.1002/aenm.20180128910.1002/aenm.201801289 ↗
42. 10.1002/adma.20150631410.1002/adma.201506314 ↗
43. 10.1002/adfm.20160367410.1002/adfm.201603674 ↗
44. 10.1007/s12274-019-2582-610.1007/s12274-019-2582-6 ↗
45. 10.1021/acsami.7b1612510.1021/acsami.7b16125 ↗
46. 10.1002/admi.20180035910.1002/admi.201800359 ↗
47. 10.1039/C9TA06861A10.1039/C9TA06861A ↗
48. 10.1021/jacs.5b0359010.1021/jacs.5b03590 ↗
49. 10.1016/j.apcatb.2019.01.03510.1016/j.apcatb.2019.01.035 ↗
50. 10.1016/j.apcatb.2018.08.05710.1016/j.apcatb.2018.08.057 ↗
51. 10.1021/acsami.0c0398310.1021/acsami.0c03983 ↗
52. 10.1016/j.cclet.2020.03.07610.1016/j.cclet.2020.03.076 ↗
53. 10.1021/acsami.0c0212410.1021/acsami.0c02124 ↗