光催化
煅烧
纳米颗粒
相(物质)
材料科学
吸附
化学工程
六方晶系
碳纤维
纳米技术
催化作用
化学
物理化学
有机化学
复合材料
结晶学
工程类
复合数
作者
Jinfeng Liu,Ping Wang,Jiajie Fan,Huogen Yu,Jiaguo Yu
出处
期刊:Nano Research
[Springer Science+Business Media]
日期:2020-11-13
卷期号:14 (4): 1095-1102
被引量:72
标识
DOI:10.1007/s12274-020-3156-3
摘要
Hexagonal molybdenum carbide (Mo2C) as an effective non-noble cocatalyst is intensively researched in the photocatalytic H2-evolution field owing to its Pt-like H+-adsorption ability and good conductivity. However, hexagonal Mo2C-modified photocatalysts possess a limited H2-evolution rate because of the weak H-desorption ability. To further improve the activity, cubic MoC was introduced into Mo2C to form the carbon-modified MoC-Mo2C nanoparticles (MoC-Mo2C@C) by a calcination method. The resultant MoC-Mo2C@C (ca. 5 nm) was eventually coupled with TiO2 to acquire high-efficiency TiO2/MoC-Mo2C@C by electrostatic self-assembly. The highest H2-generation rate of TiO2/MoC-Mo2C@C reached of 918 μmol·h−1·g−1, which was 91.8, 2.7, and 1.5 times than that of the TiO2, TiO2/MoC@C, and TiO2/Mo2C@C, respectively. The enhanced rate of TiO2 attributes to the carbon layer as cocatalyst to transmit electrons and the hetero-phase MoC-Mo2C as H2-generation active sites to boost H2-evolution reaction. This research offers a novel insight to design photocatalytic materials for energy applications.
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