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Preparation of dendritic CuNi@CF catalysts by one-step electrodeposition: Achieve efficient hydrogen evolution reaction from seawater
被引:0
|作者:
Sun, Shengwei
[1
]
Feng, Lingling
[1
]
Wang, Jing
[1
]
Wang, Shiru
[1
]
Wang, Yan
[1
]
Song, Shan
[1
]
Zhang, Ying
[1
]
Wang, Tianshuo
[1
]
Yuan, Yubin
[1
]
Zhou, Junshuang
[1
]
Gao, Faming
[1
,2
]
机构:
[1] Yanshan Univ, Sch Environm & Chem Engn, Hebei Key Lab Appl Chem, State Key Lab Metastable Mat Sci & Technol, Qinhuangdao 066004, Peoples R China
[2] Tianjin Univ Sci & Technol, Tianjin Key Lab Multiplexed Identificat Port Hazar, Tianjin 300457, Peoples R China
关键词:
Electrodeposition;
Dendrimer;
Hydrogen evolution reaction;
Seawater electrolysis;
ENERGY;
COPPER;
ELECTROCATALYST;
STRATEGIES;
REDUCTION;
DESIGN;
OXIDE;
FOAM;
D O I:
10.1016/j.seppur.2024.129171
中图分类号:
TQ [化学工业];
学科分类号:
0817 ;
摘要:
Seawater electrolysis can address the freshwater crisis and promote sustainable development, but there are several challenges, such as low catalyst activity and susceptibility to corrosion. We synthesized self-supported CuNi@CF catalysts on copper foam surfaces using a one-step electrodeposition method. In simulated seawater (6 M KOH+0.5 M NaCl), CuNi@CF showed excellent performance in the hydrogen evolution reaction with a low overpotential of 14 mV at 100 mA cm- 2, outperforming Pt/C@CF (148 mV) and most reported catalysts. The enhanced catalytic activity is attributed to the introduction of copper, which enhances electron transfer and forms a dendritic morphology with high surface area and active sites. We optimized the Ni/Cu ratio to determine the optimal experimental conditions. Corrosion tests validated the durability of CuNi@CF, showing a tiny potential drop after 100 h. The dendritic structure and Raman spectroscopy analysis supported the stability of the catalyst. The CuNi@CF||NiFe LDH electrolyzer also demonstrated excellent water decomposition efficiency in simulated seawater at 80 degrees C. This study thus presents promising prospects for hydrogen production via seawater electrolysis.
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