journal article·2025-02

Constructing RuNi‐MoO2 Heterojunction with Optimal Built‐In Electrical Field for Efficient Hydrogen Production in Anion Exchange Membrane Water Electrolyzer

Peng Guo, Pengan Zhang, Shoufu Cao, Wenjing Huang, Xiaoqing Lu, Bo Zhang, Weizhe Chen, Youzi Zhang, Yijin Wang, Ruiqing Zou, Xuanhua Li

Advanced Functional Materials· Volume 35· Issue 7
Publisher page

Abstract

Abstract Water electrolysis in alkaline media, demonstrating robust facility and cheap electrolyzer construction, are regarded as a promising strategy for industrial green hydrogen generation. Exploring effective alkaline hydrogen evolution electrocatalysts is remained an obstacle to date, which requires additional effort to obtain active hydrogen by water dissociation and promote the following unfavorable hydrogen coupling for further H2 release. Herein, the MoO2 supported RuNi nanoparticle (RuNi‐MoO2) is constructed as an efficient electrocatalyst for hydrogen evolution. Experimental and theoretical analysis demonstrate that the optimized built‐in electric field at the interface between MoO2 and RuNi alloy simultaneously accelerates the water dissociation kinetics and hydrogen spillover. It attains the current densities of 10 and 100 mA cm−2 at ultralow potential of −0.019 and −0.086 V versus RHE, respectively, along with rapid water cleavage kinetics, which even surpasses the commercial Pt/C. The constructing anion exchange membrane water electrolyzer adopting the RuNi‐MoO2 as a cathode electrocatalyst attains an industrial current density of 1 A cm−2 at a low voltage of 1.71 V and steadily operates over 1000 h with a large current density over 1 A cm−2.
Source: crossref · Quality: baseline

Research context

OpenAlex topics: Electrocatalysts for Energy Conversion · Fuel Cells and Related Materials · Hybrid Renewable Energy Systems

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

Affiliations

State Key Laboratory of Solidification Processing Center for Nano Energy Materials School of Materials Science and Engineering Northwestern Polytechnical University Xi'an 710072 P.R. China

Research and Development Institute of Northwestern Polytechnical University Shenzhen 518057 P.R. China

School of Materials Science and Engineering China University of Petroleum (East China) Qingdao 266580 P.R. China

Guangzhou Key Laboratory of Low‐Dimensional Materials and Energy Storage Devices Collaborative Innovation Center of Advanced Energy Materials School of Materials and Energy Guangdong University of Technology Guangzhou 510006 P.R. China

Funding

National Natural Science Foundation of China

References (58)

Show source-provided references
1. 10.1126/science.ade149910.1126/science.ade1499 ↗
2. 10.1038/s41560-023-01409-210.1038/s41560-023-01409-2 ↗
3. 10.1002/adma.20190638410.1002/adma.201906384 ↗
4. 10.1039/D0EE02485F10.1039/D0EE02485F ↗
5. 10.1038/s41929-021-00682-210.1038/s41929-021-00682-2 ↗
6. 10.1038/nature1147510.1038/nature11475 ↗
7. 10.1039/C9EE00197B10.1039/C9EE00197B ↗
8. 10.1016/j.apcatb.2022.12119910.1016/j.apcatb.2022.121199 ↗
9. 10.1016/j.apcatb.2022.12160310.1016/j.apcatb.2022.121603 ↗
10. 10.1126/science.aad499810.1126/science.aad4998 ↗
11. 10.1021/jacs.0c0220210.1021/jacs.0c02202 ↗
12. 10.1021/acsnano.2c0090110.1021/acsnano.2c00901 ↗
13. 10.1002/aenm.20240313610.1002/aenm.202403136 ↗
14. 10.1002/adma.20241003910.1002/adma.202410039 ↗
15. 10.1038/s41467-020-15069-310.1038/s41467-020-15069-3 ↗
16. 10.1021/acsnano.3c0295610.1021/acsnano.3c02956 ↗
17. 10.1038/s41467-024-51370-110.1038/s41467-024-51370-1 ↗
18. 10.1002/aenm.20200286010.1002/aenm.202002860 ↗
19. 10.1021/acsenergylett.1c0276910.1021/acsenergylett.1c02769 ↗
20. 10.1039/C9EE01647C10.1039/C9EE01647C ↗
21. 10.1002/anie.20210355710.1002/anie.202103557 ↗
22. 10.1016/j.nanoen.2017.03.03210.1016/j.nanoen.2017.03.032 ↗
23. 10.1002/adfm.20240667010.1002/adfm.202406670 ↗
24. 10.1002/anie.20231631910.1002/anie.202316319 ↗
25. 10.1021/acsnano.2c0988810.1021/acsnano.2c09888 ↗
26. 10.1038/s41560-023-01242-710.1038/s41560-023-01242-7 ↗
27. 10.1002/anie.20200191910.1002/anie.202001919 ↗
28. 10.1002/anie.20161133010.1002/anie.201611330 ↗
29. 10.1038/s41467-022-34121-y10.1038/s41467-022-34121-y ↗
30. 10.1038/s41467-018-07792-910.1038/s41467-018-07792-9 ↗
31. 10.1038/s41467-021-21595-510.1038/s41467-021-21595-5 ↗
32. 10.1016/j.apcatb.2020.11882410.1016/j.apcatb.2020.118824 ↗
33. 10.1016/j.apcatb.2023.12327510.1016/j.apcatb.2023.123275 ↗
34. 10.1021/acsenergylett.9b0235910.1021/acsenergylett.9b02359 ↗
35. 10.1016/j.apcatb.2019.11844110.1016/j.apcatb.2019.118441 ↗
36. 10.1021/acsenergylett.3c0145910.1021/acsenergylett.3c01459 ↗
37. Zhu S. · Adv. Funct. Mater. · 2023
38. 10.1016/j.apcatb.2023.12268410.1016/j.apcatb.2023.122684 ↗
39. 10.1021/acsenergylett.0c0249810.1021/acsenergylett.0c02498 ↗
40. 10.1002/adfm.20230383310.1002/adfm.202303833 ↗
41. 10.1002/anie.20190101010.1002/anie.201901010 ↗
42. 10.1002/adma.20200750810.1002/adma.202007508 ↗
43. 10.1021/jacs.2c0109410.1021/jacs.2c01094 ↗
44. 10.1002/anie.20200672210.1002/anie.202006722 ↗
45. 10.1016/j.apcatb.2020.11912010.1016/j.apcatb.2020.119120 ↗
46. 10.1002/anie.20190809210.1002/anie.201908092 ↗
47. 10.1016/j.apcatb.2022.12162610.1016/j.apcatb.2022.121626 ↗
48. 10.1038/ncomms1496910.1038/ncomms14969 ↗
49. 10.1002/adma.20170627910.1002/adma.201706279 ↗
50. 10.1038/s41467-021-21956-010.1038/s41467-021-21956-0 ↗
51. 10.1016/j.nanoen.2021.10594010.1016/j.nanoen.2021.105940 ↗
52. 10.1021/jacs.7b1261510.1021/jacs.7b12615 ↗
53. 10.1002/anie.20201710210.1002/anie.202017102 ↗
54. 10.1038/s41467-018-08117-610.1038/s41467-018-08117-6 ↗
55. 10.1038/s41467-022-33007-310.1038/s41467-022-33007-3 ↗
56. 10.1038/s41467-022-28843-210.1038/s41467-022-28843-2 ↗
57. 10.1021/jacs.8b0395910.1021/jacs.8b03959 ↗
58. 10.1038/s41467-021-23750-410.1038/s41467-021-23750-4 ↗