Single Ru atoms with precise coordination on a monolayer layered double hydroxide for efficient electrooxidation catalysis

被引:171
|
作者
Wang, Zelin [1 ]
Xu, Si-Min [1 ]
Xu, Yanqi [1 ]
Tan, Ling [1 ]
Wang, Xian [1 ]
Zhao, Yufei [1 ]
Duan, Haohong [2 ]
Song, Yu-Fei [1 ,3 ]
机构
[1] Beijing Univ Chem Technol, State Key Lab Chem Resource Engn, Beijing 100029, Peoples R China
[2] Univ Oxford, Dept Chem, 12 Mansfield Rd, Oxford OX1 3TA, England
[3] Beijing Univ Chem Technol, Beijing Adv Innovat Ctr Soft Matter Sci & Engn, Beijing 100029, Peoples R China
基金
北京市自然科学基金; 中国国家自然科学基金;
关键词
PREFERENTIAL OXIDATION; WATER; NANOSHEETS; CO; HYDROFORMYLATION; ELECTROCATALYST; HYDROTALCITE; CLUSTERS; INSIGHTS; OXYGEN;
D O I
10.1039/c8sc04480e
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The catalytic properties of single-atom catalysts (SACs) can be influenced largely by the chemical environment exerted by supports. Therefore, a precise location of the single atom is essential for understanding of the reaction mechanism and design of novel SACs. However, the preparation of SACs with a precise location remains a great challenge. Herein, we report a facile one-step method to synthesize single Ru atoms supported on a monolayer NiFe-layered double hydroxide (mono-NiFe). Detailed studies demonstrate that the single Ru atoms are not dispersed randomly in the LDH structure, but are uniquely located on the top of the Fe-metal atom of mono-NiFe via three oxygen atoms. Furthermore, these SACs prove to be highly active for the hydrazine electrooxidation reaction. Density functional theory calculations demonstrate that the single Ru atoms can stabilize the hydrazine electrooxidation intermediate with one unpaired electron (*N2H3 and *N2H), thus lowering the reaction barrier for the rate-determining step. Moreover, the loading amount of single Ru atoms with a precise location can even go up to 7.0 wt% without any aggregation.
引用
收藏
页码:378 / 384
页数:7
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