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Synchronous interlayer and surface engineering of NiFe layered double hydroxides by functional ligands for boosting oxygen evolution reaction
被引:1
|作者:
Chang, Kuang
[1
]
Bai, Xue
[1
]
Liu, Jiangyong
[2
]
Wang, Jing
[1
]
Yan, Xiaodong
[1
]
机构:
[1] Jiangnan Univ, Sch Chem & Mat Engn, Key Lab Synthet & Biol Colloids, Minist Educ, Wuxi 214122, Peoples R China
[2] Yangzhou Univ, Sch Chem & Chem Engn, Yangzhou 225002, Peoples R China
基金:
中国国家自然科学基金;
关键词:
Oxygen evolution reaction;
NiFe layered double hydroxide;
Anionic ligand;
Intercalation;
Surface coordination;
ANION-EXCHANGE;
PERFORMANCE;
D O I:
10.1016/j.electacta.2024.145231
中图分类号:
O646 [电化学、电解、磁化学];
学科分类号:
081704 ;
摘要:
NiFe layered double hydroxides (LDHs) are among the most advanced electrocatalysts for oxygen evolution reaction (OER), but their catalytic activity and long-term working stability still need to be highly boosted for practical applications. Herein, an innovative strategy that combines anion intercalation/deintercalation and surface coordination is developed, which simultaneously realizes the modification of the interlay and surface properties of the NiFe LDHs by ethylenediaminetetraacetate (EDTA) and trisodium citrate (TSC). The intercalation/deintercalation of the anions engineers the interlay structure, while the surface metal-ligand coordination tunes the surface properties. Both the EDTA- and TSC-engineered NiFe LDHs exhibit highly enhanced catalytic performance, showing an overpotential of 204 and 233 mV, respectively at 10 mA cm-2 in 1.0 M KOH. The remarkable catalytic performance of the EDTA-engineered NiFe LDHs is due to the combined effect of the intercalation/deintercalation and the surface metal-EDTA coordination, while the surface TSC coordination only shows limited promoting effect on catalytic activity. In addition, the EDTA-engineered NiFe LDHs demonstrate good working stability at 100 mA cm-2.
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页数:8
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