Interstitial atom-doped NiFe alloy as pre-catalysts boost direct seawater oxygen evolution

被引:18
|
作者
Song, Lumin [1 ]
Zhang, Dan [3 ]
Miao, Hongfu [1 ]
Shi, Yue [1 ]
Wang, Mengna [1 ]
Zhao, Liang [1 ]
Zhan, Tianrong [1 ]
Lai, Jianping [1 ]
Wang, Lei [1 ,2 ]
机构
[1] Qingdao Univ Sci & Technol, Coll Chem & Mol Engn, Key Lab Base Ecochem Engn, Minist Educ,Int Sci & Technol Cooperat Base Ecoche, Qingdao 266042, Peoples R China
[2] Qingdao Univ Sci & Technol, Coll Environm & Safety Engn, Shandong Engn Res Ctr Marine Environm Corros & Saf, Qingdao 266042, Peoples R China
[3] Qufu Normal Univ, Sch Chem & Chem Engn, Key Lab Catalyt Convers & Clean Energy Univ Shando, Qufu 273165, Shandong, Peoples R China
来源
APPLIED CATALYSIS B-ENVIRONMENT AND ENERGY | 2024年 / 342卷
关键词
Interstitial atom-doped alloys; Reconstructed catalysts; Stability; High valence metal species; Direct seawater oxygen reaction;
D O I
10.1016/j.apcatb.2023.123376
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
NiFe-based materials are excellent OER electrocatalysts. However, it is difficult to stabilize anions and cations during reconstruction, which also leads to the problem of high valence metals at low levels and poor stability in direct seawater. Herein, we propose the strategy of using interstitial P atom-doped NiFe alloys (P4.8-NiFe ANs400) as pre-catalysts to stabilize anions and cations, thereby promoting the formation of abundant high-valent metal species and excellent activity and stability in direct seawater. The reconstructed P4.8-NiFe ANs-400 catalyst generates a large amount of high-valence transition metal Ni4+, which contributed to its low overpotential (214 mV) and long-term stability (100 h) in a seawater electrolyte at 100 mA cm-2. Experiments and theoretical calculations show that the interstitially doped P atoms share the charge around the Fe and the active Ni sites, optimizing the free energy of the OER intermediate and making the chlorine evolution reaction (CER) difficult to proceed.
引用
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页数:11
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