journal article·2024-11Open access

Ultrafast Construction of Interfacial Akaganéite FeOOH Phase to Enable the Long‐Term Stability of Nickel‐Iron Hydroxides for Seawater Splitting at Ampere‐Level Current Density

Zhibin Liu, Yuanyuan Li, Libin Zeng, Xianyu Peng, Dashuai Wang, Zhongjian Li, Bin Yang, Yuanyuan Li, Lecheng Lei, Yang Hou

Advanced Functional Materials· Volume 34· Issue 46

Abstract

Abstract NiFe‐based hydroxides are well‐established as efficient electrocatalysts for the oxygen evolution reaction (OER) in alkaline purified water. However, they usually degrade rapidly in seawater electrolysis because of concentrated Cl− anions in seawater. In this work, a facile approach utilizing an ultrafast dipping method is presented to fabricate durable and scalable NiFe hydroxides, enhanced by interfacial akaganéite FeOOH for seawater splitting. This study reveals significantly improved electrocatalytic stability of NiFe hydroxides at an ampere‐level current density of 1000 mA cm−2 for 100 h in alkaline seawater. It is realized by the formed FeOOH in a specific akaganéite phase whose lattice tunnels are well filled by intrinsic Cl− anions, that serve to electrostatically repel corrosive chlorides in electrolyte. This anionic design also provides superior corrosion protection for other active metal‐based OER electrocatalysts when deployed in alkaline purified water and allows for facile scaling up of the anode, facilitating the practical utilization for seawater electrolysis.
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Research context

OpenAlex topics: Copper-based nanomaterials and applications · Electronic and Structural Properties of Oxides · Advanced battery technologies research

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

Affiliations

Key Laboratory of Biomass Chemical Engineering of Ministry of Education College of Chemical and Biological Engineering Zhejiang University Hangzhou 310027 China

Institute of Zhejiang University – Quzhou Quzhou 324000 China

Wallenberg Wood Science Center Department of Fiber and Polymer Technology KTH Royal Institute of Technology Stockholm 10044 Sweden

Zhejiang University Hydrogen Energy Institute Hangzhou 310027 China

Funding

Fundamental Research Funds for the Central Universities · Innovative Research Group Project of the National Natural Science Foundation of China · National Natural Science Foundation of China

References (58)

Show source-provided references
1. 10.1002/adfm.20200388910.1002/adfm.202003889 ↗
2. 10.1002/adfm.20221094510.1002/adfm.202210945 ↗
3. 10.1021/acs.chemrev.3c0000510.1021/acs.chemrev.3c00005 ↗
4. 10.1007/s40820-024-01382-910.1007/s40820-024-01382-9 ↗
5. 10.1038/s41467-022-33847-z10.1038/s41467-022-33847-z ↗
6. 10.1002/adma.20230402210.1002/adma.202304022 ↗
7. 10.1038/s41586-022-05379-510.1038/s41586-022-05379-5 ↗
8. 10.1002/anie.20231167410.1002/anie.202311674 ↗
9. 10.1038/s41560-020-0550-810.1038/s41560-020-0550-8 ↗
10. 10.1002/smll.20231147710.1002/smll.202311477 ↗
11. 10.1016/j.nanoen.2024.10948110.1016/j.nanoen.2024.109481 ↗
12. 10.1016/j.joule.2023.03.00510.1016/j.joule.2023.03.005 ↗
13. 10.1002/cssc.20150158110.1002/cssc.201501581 ↗
14. 10.1038/s41560-023-01409-210.1038/s41560-023-01409-2 ↗
15. 10.1002/anie.20221075310.1002/anie.202210753 ↗
16. 10.1016/j.renene.2022.03.13710.1016/j.renene.2022.03.137 ↗
17. 10.1021/acs.chemrev.1c0085410.1021/acs.chemrev.1c00854 ↗
18. 10.1016/j.jechem.2023.11.00110.1016/j.jechem.2023.11.001 ↗
19. 10.1016/j.jpowsour.2019.22737510.1016/j.jpowsour.2019.227375 ↗
20. 10.1016/j.electacta.2023.14326910.1016/j.electacta.2023.143269 ↗
21. 10.1021/acssuschemeng.2c0035910.1021/acssuschemeng.2c00359 ↗
22. 10.1073/pnas.190055611610.1073/pnas.1900556116 ↗
23. 10.1002/anie.20211035510.1002/anie.202110355 ↗
24. 10.1039/D0EE00921K10.1039/D0EE00921K ↗
25. 10.1002/smll.20230569410.1002/smll.202305694 ↗
26. 10.1016/j.apcatb.2023.12274910.1016/j.apcatb.2023.122749 ↗
27. 10.1002/anie.20230988210.1002/anie.202309882 ↗
28. 10.1002/anie.20231652210.1002/anie.202316522 ↗
29. 10.1021/acsnano.2c0387710.1021/acsnano.2c03877 ↗
30. 10.1021/acsnano.2c1193910.1021/acsnano.2c11939 ↗
31. 10.1021/acsnano.0c0421010.1021/acsnano.0c04210 ↗
32. 10.1002/aenm.20230192110.1002/aenm.202301921 ↗
33. 10.1039/C9EE03273H10.1039/C9EE03273H ↗
34. 10.1016/j.nanoen.2019.10436710.1016/j.nanoen.2019.104367 ↗
35. 10.1007/s12274-017-1886-710.1007/s12274-017-1886-7 ↗
36. 10.1002/adfm.20211267410.1002/adfm.202112674 ↗
37. 10.1021/acs.chemmater.2c0306710.1021/acs.chemmater.2c03067 ↗
38. 10.1021/am300380m10.1021/am300380m ↗
39. 10.1002/sia.198410.1002/sia.1984 ↗
40. 10.1021/acscatal.2c0445210.1021/acscatal.2c04452 ↗
41. 10.1021/acs.iecr.4c0014910.1021/acs.iecr.4c00149 ↗
42. 10.1021/ja502379c10.1021/ja502379c ↗
43. 10.1021/ja511559d10.1021/ja511559d ↗
44. 10.1073/pnas.220281211910.1073/pnas.2202812119 ↗
45. 10.1016/j.cej.2023.14529310.1016/j.cej.2023.145293 ↗
46. 10.1038/s41467-023-40563-910.1038/s41467-023-40563-9 ↗
47. Sastri V. S. · 2011
48. 10.1021/acscatal.9b0387610.1021/acscatal.9b03876 ↗
49. 10.1016/0927-0256(96)00008-010.1016/0927-0256(96)00008-0 ↗
50. 10.1103/PhysRevB.54.1116910.1103/PhysRevB.54.11169 ↗
51. 10.1103/PhysRevLett.77.386510.1103/PhysRevLett.77.3865 ↗
52. 10.1063/1.338234410.1063/1.3382344 ↗
53. 10.1021/jp047349j10.1021/jp047349j ↗
54. 10.1021/la303884610.1021/la3038846 ↗
55. Páll S. · 2015
56. 10.1016/0010-4655(95)00042-E10.1016/0010-4655(95)00042-E ↗
57. 10.1002/jcc.2029110.1002/jcc.20291 ↗
58. 10.1016/j.softx.2015.06.00110.1016/j.softx.2015.06.001 ↗