TY - JOUR
T1 - NiFe-LDH coated NiSe/Ni foam as a bifunctional electrocatalyst for overall water splitting
AU - Wu, Wentong
AU - Min, Boya
AU - Li, Hanbing
AU - Liu, Feng
AU - Zheng, Mingsheng
AU - Ding, Kunpeng
AU - Lu, Shijian
AU - Liu, Maochang
N1 - Publisher Copyright:
© 2023 The Royal Society of Chemistry.
PY - 2023/3/28
Y1 - 2023/3/28
N2 - Electrocatalytic water splitting is promising for renewable hydrogen production, yet relies on the development of a highly active and stable electrocatalyst. Herein, we report the construction of a bifunctional heterostructure electrocatalyst in the form of NiFe layered double hydroxide coated NiSe/Ni foam (NiSe@NiFe-LDH/NF) for efficient electrocatalytic water splitting. Benefiting from the superior electrical conductivity and high specific surface area of NiSe, the high active site density of NiFe-LDH, the fast charge transfer rate at a tight interface, and the strong corrosion resistance of the shell layer, NiSe@NiFe-LDH/NF exhibited excellent electrocatalytic activity and stability towards the oxygen evolution reaction (209 mV@10 mA cm−2, 241 mV@100 mA cm−2), hydrogen evolution reaction (93 mV@10 mA cm−2, 213 mV@100 mA cm−2), and overall water splitting (1.560 V@10 mA cm−2) in 1 M KOH electrolyte. This work thus provides new insights into the design of more efficient and stable bifunctional non-noble metal electrocatalysts.
AB - Electrocatalytic water splitting is promising for renewable hydrogen production, yet relies on the development of a highly active and stable electrocatalyst. Herein, we report the construction of a bifunctional heterostructure electrocatalyst in the form of NiFe layered double hydroxide coated NiSe/Ni foam (NiSe@NiFe-LDH/NF) for efficient electrocatalytic water splitting. Benefiting from the superior electrical conductivity and high specific surface area of NiSe, the high active site density of NiFe-LDH, the fast charge transfer rate at a tight interface, and the strong corrosion resistance of the shell layer, NiSe@NiFe-LDH/NF exhibited excellent electrocatalytic activity and stability towards the oxygen evolution reaction (209 mV@10 mA cm−2, 241 mV@100 mA cm−2), hydrogen evolution reaction (93 mV@10 mA cm−2, 213 mV@100 mA cm−2), and overall water splitting (1.560 V@10 mA cm−2) in 1 M KOH electrolyte. This work thus provides new insights into the design of more efficient and stable bifunctional non-noble metal electrocatalysts.
UR - https://www.scopus.com/pages/publications/85153526346
U2 - 10.1039/d3re00004d
DO - 10.1039/d3re00004d
M3 - 文章
AN - SCOPUS:85153526346
SN - 2058-9883
VL - 8
SP - 1711
EP - 1718
JO - Reaction Chemistry and Engineering
JF - Reaction Chemistry and Engineering
IS - 7
ER -