journal article·2026-04Open access

Unsaturated NiO Incorporated PtNi, Possessing Abundant Surface Hydroxyl Species, as an Efficient and Durable Electrocatalyst for the Hydrogen Evolution Reaction in Seawater

Xiong Yang, Lu Wu, Yi‐Yuan Wang, Bing‐Bing Jia, Yu‐Xuan Xiao, Ge Tian, Jie Ying, Yi Lu, Si‐Ming Wu, Wei Geng, Fei Yu, Ling Shen, Ion Tiginyanu, Xiao‐Yu Yang

Advanced Functional Materials· Volume 36· Issue 32

Abstract

ABSTRACT Creating an abundance of OH * active sites on the surface of an electrocatalyst is an ideal approach for improving both its performance and Cl – corrosion resistance in seawater splitting to generate hydrogen via the hydrogen evolution reactions (HER). However, the development of strategies for designing coordinatively saturated metals that have these sites remains a significant challenge. Herein, we report on the development of NiO/Pt 3 Ni‐300, a coordinatively unsaturated NiO incorporated Pt 3 Ni, which has the ability to capture large numbers of surface hydroxyl groups during the HER in seawater and, in consequence of this, it exhibits high electrocatalytic activity in seawater. Additionally, benefiting from super‐hydrophilicity induced by its rich OH * surface, NiO/Pt 3 Ni‐300 preferentially adsorbs H 2 O over Cl – . The outstanding HER performance of this catalyst in alkaline seawater is reflected by a low overpotential of 16 mV to drive a current density of 10 mA cm −2 , and a 7.7‐fold higher turnover frequency compared to that of Pt/C. Moreover, it displays only a small 41 mV drop in overpotential after promotion of the HER for 20 h in alkaline seawater, a value that surpasses those inherent to commercial Pt/C, Pt 3 Ni, and crystalline NiO incorporated Pt 3 Ni.
Source: crossref · Quality: baseline

Research context

OpenAlex topics: Electrocatalysts for Energy Conversion · Ammonia Synthesis and Nitrogen Reduction · Hybrid Renewable Energy Systems

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

Affiliations

State Key Laboratory of Advanced Technology for Materials Synthesis and Processing & School of Chemistry, Chemical Engineering and Life Sciences & International School of Materials Science and Engineering Wuhan University of Technology Wuhan China

School of Chemical Engineering and Technology Sun Yat‐sen University Zhuhai China

National Energy Key Laboratory for New Hydrogen‐Ammonia Energy Technologies Foshan Xianhu Laboratory Foshan China

National Center for Materials Study and Testing Technical University of Moldova Chisinau Republic of Moldova

Funding

National Natural Science Foundation of China · Basic and Applied Basic Research Foundation of Guangdong Province · Shenzhen Science and Technology Innovation Program

References (51)

Show source-provided references
1. 10.1002/adfm.20241566010.1002/adfm.202415660 ↗
2. 10.1002/adma.20200384610.1002/adma.202003846 ↗
3. 10.1021/acsenergylett.9b0022010.1021/acsenergylett.9b00220 ↗
4. 10.1039/D3EE03363E10.1039/D3EE03363E ↗
5. 10.1002/anie.20231167410.1002/anie.202311674 ↗
6. 10.1021/acs.chemmater.1c0440010.1021/acs.chemmater.1c04400 ↗
7. 10.1002/chem.20220281110.1002/chem.202202811 ↗
8. 10.1007/s11705‐023‐2300‐510.1007/s11705‐023‐2300‐5 ↗
9. 10.1021/acsnano.2c1184410.1021/acsnano.2c11844 ↗
10. 10.1002/adma.20220177410.1002/adma.202201774 ↗
11. 10.1007/s40843‐023‐2566‐y10.1007/s40843‐023‐2566‐y ↗
12. 10.1016/j.apmate.2024.10022710.1016/j.apmate.2024.100227 ↗
13. 10.1002/adfm.20241826410.1002/adfm.202418264 ↗
14. 10.1021/acs.chemmater.3c0134810.1021/acs.chemmater.3c01348 ↗
15. 10.1021/acsnano.3c0517410.1021/acsnano.3c05174 ↗
16. 10.1039/D4EE00950A10.1039/D4EE00950A ↗
17. 10.1016/j.molstruc.2012.11.01310.1016/j.molstruc.2012.11.013 ↗
18. 10.1021/cr500310b10.1021/cr500310b ↗
19. 10.1039/D4CC04333B10.1039/D4CC04333B ↗
20. 10.1016/j.jechem.2023.12.01810.1016/j.jechem.2023.12.018 ↗
21. 10.1006/jcis.2001.786410.1006/jcis.2001.7864 ↗
22. 10.1021/jacs.0c0024110.1021/jacs.0c00241 ↗
23. 10.1021/jacs.8b0477010.1021/jacs.8b04770 ↗
24. 10.1002/anie.20160629010.1002/anie.201606290 ↗
25. 10.1002/adfm.20252359210.1002/adfm.202523592 ↗
26. 10.1016/j.apcatb.2022.12187910.1016/j.apcatb.2022.121879 ↗
27. 10.1002/anie.20240143410.1002/anie.202401434 ↗
28. 10.1016/j.cej.2023.14563010.1016/j.cej.2023.145630 ↗
29. 10.1073/pnas.231942712110.1073/pnas.2319427121 ↗
30. 10.1038/s41586‐022‐05296‐710.1038/s41586‐022‐05296‐7 ↗
31. 10.1002/anie.20150283610.1002/anie.201502836 ↗
32. 10.1002/adma.20180512710.1002/adma.201805127 ↗
33. 10.1016/j.apcatb.2020.11980910.1016/j.apcatb.2020.119809 ↗
34. 10.1038/nmat345810.1038/nmat3458 ↗
35. 10.1126/science.124906110.1126/science.1249061 ↗
36. 10.1016/j.apcatb.2019.11808010.1016/j.apcatb.2019.118080 ↗
37. 10.1016/j.nanoen.2017.07.03210.1016/j.nanoen.2017.07.032 ↗
38. 10.1039/D0CC06876D10.1039/D0CC06876D ↗
39. 10.1039/D3CC05959F10.1039/D3CC05959F ↗
40. 10.1039/C7EE03603E10.1039/C7EE03603E ↗
41. 10.1039/D4TA08772K10.1039/D4TA08772K ↗
42. 10.1073/pnas.190055611610.1073/pnas.1900556116 ↗
43. 10.1021/acs.nanolett.1c0226810.1021/acs.nanolett.1c02268 ↗
44. 10.1021/acs.jpcc.7b0216610.1021/acs.jpcc.7b02166 ↗
45. 10.1002/adma.20230449610.1002/adma.202304496 ↗
46. 10.1021/acs.nanolett.5c0041710.1021/acs.nanolett.5c00417 ↗
47. 10.1007/s40843‐025‐3389‐310.1007/s40843‐025‐3389‐3 ↗
48. 10.1038/s41467‐022‐31474‐210.1038/s41467‐022‐31474‐2 ↗
49. 10.1103/PhysRevB.50.1795310.1103/PhysRevB.50.17953 ↗
50. 10.1002/jcc.2111210.1002/jcc.21112 ↗
51. 10.1021/jp111930w10.1021/jp111930w ↗