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Metastable Phase Noble-Metal-Free Core-Shell Structure for Efficient Electrocatalytic Nitrobenzene Transfer Hydrogenation
被引:0
|作者:
Xiong, Yutian
[1
]
Chen, Jinxin
[2
]
Wang, Yue
[1
]
Wang, Qun
[2
]
Liu, Da
[1
]
Shao, Qi
[1
]
Lu, Jianmei
[1
]
机构:
[1] Soochow Univ, Coll Chem Chem Engn & Mat Sci, Suzhou 215123, Jiangsu, Peoples R China
[2] Soochow Univ, Inst Funct Nano & Soft Mat FUNSOM, Jiangsu Key Lab Carbon Based Funct Mat & Devices, Suzhou 215123, Jiangsu, Peoples R China
基金:
中国国家自然科学基金;
关键词:
Electrocatalytic hydrogenationof nitrobenzene reaction;
Metastable phases;
Core-shellstructures;
Noble-metal-free catalysts;
PATHWAYS;
NICKEL;
D O I:
10.1021/acs.nanolett.4c04966
中图分类号:
O6 [化学];
学科分类号:
0703 ;
摘要:
In order to study the catalytic behavior of a metastable-phase catalyst in electrocatalytic hydrogenation, we report a new metastable-phase noble-metal-free core-shell catalyst with a metastable hexagonal closest packed (hcp) phase Ni as the shell and face-centered-cubic (fcc) phase Cu as the core (Cu@hcp Ni NPs) for electrocatalytic hydrogenation of nitrobenzene (Ph-NO2) to aniline (Ph-NH2). Using H2O as the hydrogen source, it achieves up to 99.63% Ph-NO2 conversion and similar to 100% Ph-NH2 selectivity, with an improved activity turnover frequency (TOF: 6640 h-1), much higher than those of hcp Ni NPs (5183.7 h-1) and commercial Pt/C (3537.6 h-1). It can also deliver a variety of aminoarenes with outstanding selectivity and excellent functional group compatibility with several groups. Mechanistic studies have shown that the introduction of Cu enhances hcp Ni's ability to dissociate water in situ to produce H* and improves the hydrogenation rate, resulting in the rapid conversion of Ph-NO2 to the final product Ph-NH2.
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页码:3383 / 3390
页数:8
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