journal article·2022-01-24

WO3 Nanosheet-Supported IrW Alloy for High-Performance Acidic Overall Water Splitting with Low Ir Loading

Dinghua Zhou, Min He, Yunxuan Ding, Jiaguo Yu, Ke Fan, Licheng Sun

ACS Applied Energy Materials· Volume 5· Issue 1
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Abstract

Precious metals (like Ir, Ru, and Pt) and their derivatives are the benchmark catalysts for water splitting in acidic media due to their high stability and activity. However, the high cost and scarcity of these materials hamper the large-scale applications. To solve this issue, construction of catalysts containing low content of precious metals with high intrinsic activity can be an efficient strategy, which expectedly can decrease the cost but meanwhile preserve the activity. Herein, we synthesized an IrW/WO3 array catalyst by in situ formation of IrW alloy on hierarchical WO3 nanosheet arrays. With extremely low Ir content of 1.25 wt % in 0.5 M H2SO4, this composite catalyst not only shows superior water oxidation activity (the overpotential at 10 mA cm–2 is only 229 mV, significantly lower than that of the commercial IrO2 (358 mV)) but also exhibits excellent proton reduction performance (the overpotential at −10 mA cm–2 is 49 mV, close to that of commercial Pt/C catalyst (42 mV)), showing promising bifunctionality for the overall water splitting. As a result, only 1.5 V is needed to drive the overall water splitting at 10 mA cm–2 with a good long-term stability under acidic conditions. These remarkable features can be ascribed to the abundant active sites exposed by the three-dimensional nanostructure, and the high intrinsic activity per Ir site. The theoretical calculation verifies that Ir sites in IrW surface after oxidation have a higher intrinsic activity than IrO2 for water oxidation. We believe this research can supply a strategy to design highly active and stable catalysts with low loading of noble metals for acidic water splitting.
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Research context

OpenAlex topics: Electrocatalysts for Energy Conversion · Advanced Photocatalysis Techniques · Copper-based nanomaterials and applications

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

Affiliations

State Key Laboratory of Fine Chemicals, Institute of Artificial Photosynthesis, DUT-KTH Joint Education and Research Centre on Molecular Devices, Institute for Energy Science and Technology, Dalian University of Technology, 116024 Dalian, China

State Key Laboratory of Advanced Technology for Materials Synthesis and Processing, Wuhan University of Technology, Wuhan 430070, P.R. China

Center of Artificial Photosynthesis for Solar Fuels, School of Science, Westlake University, 310024 Hangzhou, China

Department of Chemistry, KTH Royal Institute of Technology, Stockholm 10044, Sweden

Funding

Vetenskapsr?det · Knut och Alice Wallenbergs Stiftelse · Central University Basic Research Fund of China · National Natural Science Foundation of China · Key Laboratory of Bio-based Chemicals of Liaoning Province

References (47)

Show source-provided references
1. 10.1002/aenm.20200047810.1002/aenm.202000478 ↗
2. 10.1002/adma.20200632810.1002/adma.202006328 ↗
3. 10.1039/C9NR07832K10.1039/C9NR07832K ↗
4. 10.1002/adma.20190143910.1002/adma.201901439 ↗
5. 10.1038/s41467-018-05341-y10.1038/s41467-018-05341-y ↗
6. 10.1016/j.mtener.2018.11.00110.1016/j.mtener.2018.11.001 ↗
7. 10.1016/j.nanoen.2017.06.03210.1016/j.nanoen.2017.06.032 ↗
8. 10.1002/adma.20200424310.1002/adma.202004243 ↗
9. 10.1039/D1TA02597J10.1039/D1TA02597J ↗
10. 10.1002/aenm.20210238810.1002/aenm.202102388 ↗
11. 10.1038/s41893-020-0509-610.1038/s41893-020-0509-6 ↗
12. 10.1039/D0EE00877J10.1039/D0EE00877J ↗
13. 10.1038/s41560-018-0209-x10.1038/s41560-018-0209-x ↗
14. 10.1021/acsaem.0c0020110.1021/acsaem.0c00201 ↗
15. 10.1021/jacs.5b0778810.1021/jacs.5b07788 ↗
16. 10.1039/C4NR04072D10.1039/C4NR04072D ↗
17. 10.1021/acs.chemmater.8b0362010.1021/acs.chemmater.8b03620 ↗
18. 10.1039/C9SE01282F10.1039/C9SE01282F ↗
19. 10.1039/D1CY00650A10.1039/D1CY00650A ↗
20. 10.1039/C6TA08075H10.1039/C6TA08075H ↗
21. 10.1002/adfm.20150562610.1002/adfm.201505626 ↗
22. 10.1021/acscentsci.8b0042610.1021/acscentsci.8b00426 ↗
23. 10.1039/C7TA04923D10.1039/C7TA04923D ↗
24. 10.1021/acssuschemeng.9b0119910.1021/acssuschemeng.9b01199 ↗
25. 10.1038/s41467-018-03429-z10.1038/s41467-018-03429-z ↗
26. 10.1039/D0TA08802A10.1039/D0TA08802A ↗
27. 10.1039/C7EE02626A10.1039/C7EE02626A ↗
28. 10.1021/jp074219c10.1021/jp074219c ↗
29. 10.1149/1.183854810.1149/1.1838548 ↗
30. 10.1021/acscatal.6b0234310.1021/acscatal.6b02343 ↗
31. 10.1088/1361-6463/ac0b7310.1088/1361-6463/ac0b73 ↗
32. 10.1016/j.matlet.2016.09.08310.1016/j.matlet.2016.09.083 ↗
33. 10.1038/s41467-021-23907-110.1038/s41467-021-23907-1 ↗
34. 10.1038/s41586-021-03454-x10.1038/s41586-021-03454-x ↗
35. 10.1002/anie.20160068710.1002/anie.201600687 ↗
36. 10.1021/acsami.8b1197010.1021/acsami.8b11970 ↗
37. 10.1021/acs.chemmater.9b0201110.1021/acs.chemmater.9b02011 ↗
38. 10.1039/C7TA08982A10.1039/C7TA08982A ↗
39. 10.1002/adma.20170379810.1002/adma.201703798 ↗
40. 10.1002/adfm.20190115410.1002/adfm.201901154 ↗
41. 10.1021/jacs.8b1145610.1021/jacs.8b11456 ↗
42. 10.1021/acscatal.0c0411710.1021/acscatal.0c04117 ↗
43. 10.1103/PhysRevB.54.1116910.1103/PhysRevB.54.11169 ↗
44. 10.1103/PhysRevB.59.175810.1103/PhysRevB.59.1758 ↗
45. 10.1103/PhysRevB.50.1795310.1103/PhysRevB.50.17953 ↗
46. 10.1103/PhysRevLett.77.386510.1103/PhysRevLett.77.3865 ↗
47. 10.1021/acscatal.9b0191010.1021/acscatal.9b01910 ↗