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Energetic MOF-derived Fe3C nanoparticles encased in N,S-codoped mesoporous pod-like carbon nanotubes for efficient oxygen reduction reaction
被引:0
|作者:
Liu, Yang
[1
]
Duan, Xinde
[1
]
Ge, Fayuan
[1
]
Wu, Tingting
[1
]
Zheng, Hegen
[1
]
机构:
[1] Nanjing Univ, Collaborat Innovat Ctr Adv Microstruct, Sch Chem & Chem Engn, State Key Lab Coordinat Chem, Nanjing 210023, Peoples R China
来源:
基金:
中国国家自然科学基金;
关键词:
METAL-ORGANIC FRAMEWORKS;
SITES;
ELECTROCATALYST;
CO;
D O I:
10.1039/d4nr04004j
中图分类号:
O6 [化学];
学科分类号:
0703 ;
摘要:
The rational design of advanced oxygen reduction reaction (ORR) catalysts is essential to improve the performance of energy conversion devices. However, it remains a huge challenge to construct hierarchical micro-/meso-/macroporous nanostructures, especially mesoporous transport channels in catalysts, to enhance catalytic capability. Herein, motivated by the characteristics of energetic metal-organic frameworks (EMOFs) that produce an abundance of gases during high-temperature pyrolysis, we prepared a unique tetrazine-based EMOF-derived electrocatalyst (denoted as Fe3C@NSC-900) consisting of highly dispersed Fe3C nanoparticles and N,S-codoped mesoporous carbon nanotubes. The mesopore-dominated core-shell structure endows Fe3C@NSC-900 with excellent catalytic activity and efficient mass transfer. Thus, optimal Fe3C@NSC-900 demonstrates a high half-wave potential of 0.922 V and great stability in 0.1 M KOH, outperforming commercial Pt/C and most of the reported ORR catalysts. As far as we know, this work is the first application of a tetrazine-based EMOF derivative for the electrocatalytic ORR and is expected to offer some constructive insights into potential of EMOFs for new-generation catalyst design.
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页码:3941 / 3948
页数:8
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