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A Bioinspired Hierarchical Fast Transport Network Boosting Electrochemical Performance of 3D Printed Electrodes
被引:5
|作者:
Zhao, Bo
[1
]
Wu, Jiawen
[1
]
Liang, Zhiqiang
[1
]
Liang, Wenkai
[1
]
Yang, He
[1
]
Li, Dan
[1
]
Qin, Wei
[1
]
Peng, Meiwen
[1
]
Sun, Yinghui
[2
]
Jiang, Lin
[1
]
机构:
[1] Soochow Univ, Inst Funct Nano & Soft Mat FUNSOM, Jiangsu Key Lab Carbon Based Funct Mat & Devices, Suzhou 215123, Jiangsu, Peoples R China
[2] Soochow Univ, Coll Energy, Soochow Inst Energy & Mat Innovat, Key Lab Adv Carbon Mat & Wearable Energy Technol, Suzhou 215006, Jiangsu, Peoples R China
基金:
中国国家自然科学基金;
国家重点研发计划;
关键词:
3D printing;
biomimetic materials;
electrochemical electrodes;
mass transport;
water splitting;
ELECTROCATALYSTS;
NANOSHEETS;
D O I:
10.1002/advs.202204751
中图分类号:
O6 [化学];
学科分类号:
0703 ;
摘要:
Current 3D printed electrodes suffer from insufficient multiscale transport speed, which limits the improvement of electrochemical performance of 3D printed electrodes. Herein, a bioinspired hierarchical fast transport network (HFTN) in a 3D printed reduced graphene oxide/carbon nanotube (3DP GC) electrode demonstrating superior electrochemical performance is constructed. Theoretical calculations reveal that the HFTN of the 3DP GC electrode increases the ion transport rate by more than 50 times and 36 times compared with those of the bulk GC electrode and traditional 3DP GC (T-3DP GC) electrode, respectively. Compared with carbon paper, carbon cloth, bulk GC electrode, and T-3DP GC electrode, the HFTN in 3DP GC electrode endows obvious advantages: i) efficient utilization of surface area for uniform catalysts dispersion during electrochemical deposition; ii) efficient utilization of catalysts enables the high mass activity of catalysts and low overpotential of electrode in electrocatalytic reaction. The cell of 3DP GC/Ni-NiO||3DP GC/NiS2 demonstrates a low voltage of only 1.42 V to reach 10 mA cm(-2) and good stability up to 20 h for water splitting in alkaline conditions, which is superior to commercialized Pt/C||RuO2. This work demonstrates great potential in developing high-performance 3D printed electrodes for electrochemical energy conversion and storage.
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