Sulfidation adjust the valence states of metal ions enhancing alkaline seawater OER catalytic activity and stability for PBA-derived self-supporting NiFe sulfide

被引:0
作者
Tong, Xuan [1 ]
Xu, Haiyang [1 ]
Wei, Shengjie [1 ]
Sun, Dingcheng [2 ]
Lin, Shan [2 ]
Zhou, Hangyu [2 ]
Ji, Xu [1 ,2 ]
Yang, Yue [1 ,3 ]
Zhang, Le [2 ,3 ]
机构
[1] Yunnan Normal Univ, Sch Phys & Elect Informat, Kunming 650500, Peoples R China
[2] Yunnan Normal Univ, Sch Energy & Environm Sci, Kunming 650500, Peoples R China
[3] Yunnan Normal Univ, Key Lab Renewable Energy Adv Mat & Mfg Technol, Educ Minist, Kunming 650500, Peoples R China
关键词
Oxygen evolution reaction; Prussian blue analogue; Sulfidation; Seawater; REDUCTION; HYDROXIDE;
D O I
10.1016/j.mssp.2025.109396
中图分类号
TM [电工技术]; TN [电子技术、通信技术];
学科分类号
0808 ; 0809 ;
摘要
Seawater, a prevalent resource, is gaining attention as a substitute for freshwater in hydrogen electrolysis. Nonetheless, the corrosion resistance of the anode to chloride ions still faces challenges. In this paper, NiFe PBAS/NF was grown on nickel foam to promote effective electron conduction between the substrate and the catalyst, and the catalyst was enriched with redox reaction by adjusting the valence state of metal ions through sulfidation, which was beneficial to electrocatalytic kinetics and durability. Notably, it exhibited excellent performance in alkaline simulated seawater electrolytes, with an overpotential of 247 mV at 100 mA cm- 2 and remained stable for more than 55 h. In addition, we evaluated the effect of Cl-ion concentration on catalyst performance and observed that the catalyst exhibited higher OER activity in alkaline simulated seawater with higher concentrations of Cl-. These results provide a solid experimental foundation for designing economically efficient seawater corrosion resistant electrolytic catalysts.
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页数:8
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