Interface electron collaborative migration of Co-Co3O4/carbon dots: Boosting the hydrolytic dehydrogenation of ammonia borane

被引:81
|
作者
Wu, Han [1 ,2 ]
Wu, Min [3 ]
Wang, Boyang [1 ]
Yong, Xue [4 ]
Liu, Yushan [1 ]
Li, Baojun [1 ]
Liu, Baozhong [2 ]
Lu, Siyu [1 ]
机构
[1] Zhengzhou Univ, Coll Chem, Zhengzhou 450001, Henan, Peoples R China
[2] Henan Polytech Univ, Coll Chem & Chem Engn, Jiaozuo 454000, Henan, Peoples R China
[3] Zhejiang Univ Technol, Coll Mat Sci & Engn, Hangzhou 310014, Zhejiang, Peoples R China
[4] Univ Saskatchewan, Dept Phys & Engn Phys, Saskatoon, SK S7N E2, Canada
来源
基金
中国国家自然科学基金; 中国博士后科学基金;
关键词
CARBON QUANTUM DOTS; HYDROGEN EVOLUTION REACTION; CORE-SHELL NANOPARTICLES; METAL-ORGANIC FRAMEWORKS; IN-SITU SYNTHESIS; CATALYTIC-ACTIVITY; GRAPHENE; GENERATION; COMPOSITE; OXIDE;
D O I
10.1016/j.jechem.2019.12.023
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
Ammonia borane (AB) is an excellent candidate for the chemical storage of hydrogen. However, its practical utilization for hydrogen production is hindered by the need for expensive noble-metal-based catalysts. Herein, we report Co–Co3O4 nanoparticles (NPs) facilely deposited on carbon dots (CDs) as a highly efficient, robust, and noble-metal-free catalyst for the hydrolysis of AB. The incorporation of the multi-interfaces between Co, Co3O4 NPs, and CDs endows this hybrid material with excellent catalytic activity (rB = 6816mLH min–1 gCo–1) exceeding that of previous non-noble-metal NP systems and even that of some noble-metal NP systems. A further mechanistic study suggests that these interfacial interactions can affect the electronic structures of interfacial atoms and provide abundant adsorption sites for AB and water molecules, resulting in a low energy barrier for the activation of reactive molecules and thus substantial improvement of the catalytic rate. © 2020
引用
收藏
页码:43 / 53
页数:11
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