A Critical Review on New and Efficient 2D Materials for Catalysis

被引:20
|
作者
Zhao, Liping [1 ]
Wang, Bingquan [2 ]
Wang, Rui [1 ]
机构
[1] Shandong Univ, Sch Environm Sci & Engn, Qingdao 266237, Peoples R China
[2] Qingdao Univ Sci & Technol Qingdao, Sch Chem & Mol Engn, Qingdao 266042, Peoples R China
来源
ADVANCED MATERIALS INTERFACES | 2022年 / 9卷 / 29期
关键词
black phosphorus; boron nitride; catalytic reaction; graphene; MXenes; transition metal dichalcogenides; LIGHT PHOTOCATALYTIC ACTIVITY; HEXAGONAL BORON-NITRIDE; REDUCED GRAPHENE OXIDE; 2-DIMENSIONAL MOLYBDENUM CARBIDE; BLACK PHOSPHORUS NANOSHEETS; OXYGEN REDUCTION REACTION; METAL-ORGANIC FRAMEWORKS; HYDROGEN EVOLUTION; CARBON NITRIDE; H-2; EVOLUTION;
D O I
10.1002/admi.202200771
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The unique structure and properties of graphene make it have excellent performance in the field of catalysis. It can be modified in various ways to improve its catalytic ability. Notably, other 2D materials with similar properties to graphene (black phosphorus (BP), 2D transition metal dichalcogenides represented by molybdenum disulfide (MoS2) and tungsten disulfide (WS2), boron nitride (BN), and transition metal carbide and nitride (MXenes) and their hybrid materials also have a wide range of applications in the field of catalysis. In general, 2D materials can be used as catalysts, catalytic supports or electron donors. Therefore, they have been widely used in many catalytic reactions in recent years, such as photocatalysis, thermocatalysis, and electrocatalysis. In this paper, the research progress of the above 2D materials in the catalytic degradation of organic matter in water and carbon dioxide reduction reaction (CO2RR) is summarized. In addition, some excellent composite 2D catalysts in the fields of photocatalysis and electrocatalysis are summarized and compared. Finally, the opportunities and challenges of the above 2D materials in the field of catalysis are pointed out, and the development prospects of the 2D materials in the field of catalysis are addressed.
引用
收藏
页数:33
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