Cu Nanocluster-Loaded TiO2 Nanosheets for Highly Efficient Generation of CO-Free Hydrogen by Selective Photocatalytic Dehydrogenation of Methanol to Formaldehyde

被引:30
作者
Yu, Fengyang [1 ]
Chen, Liyong [1 ]
Li, Xuezhao [1 ]
Shen, Xiaoshuang [2 ]
Zhao, He [3 ]
Duan, Chunying [1 ]
Chen, Qianwang [4 ]
机构
[1] Dalian Univ Technol, State Key Lab Fine Chem, Dalian 116024, Peoples R China
[2] Yangzhou Univ, Sch Phys Sci & Technol, Yangzhou 225002, Jiangsu, Peoples R China
[3] Dalian Univ Technol, Div Chem, Dalian 116024, Peoples R China
[4] Univ Sci & Technol China, Dept Mat Sci & Engn, Hefei Natl Lab Phys Sci Microscale, Hefei 230026, Peoples R China
基金
中国国家自然科学基金;
关键词
Cu nanocluster; TiO2; nanosheet; HKUST-1; photocatalytic dehydrogenation; hydrogen evolution; METAL-ORGANIC FRAMEWORKS; ANATASE TIO2; WATER; NANOPARTICLES; AU; CONVERSION; COPPER; ADSORPTION; PERCENTAGE; OXIDATION;
D O I
10.1021/acsami.0c20116
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Safe storage and transportation of H-2 is a fundamental requirement for its wide applications in the future. Controllable release of high-purity H-2 from a stable storage medium such as CH3OH before use offers an efficient way of achieving this purpose. In our case, Cu nanoclusters uniformly dispersed onto (001) surfaces of TiO2 nanosheets (TiO2/Cu) are selectively prepared by thermal treatment of HKUST-1 loaded TiO2 nanosheets. One of the TiO2/Cu composites, TiO2/Cu_50, exhibits remarkably high activity toward the selective dehydrogenation of CH3OH to HCHO with a H-2 evolution rate of 17.8 mmol h(-1) per gram of catalyst within a 16-h photocatalytic reaction (quantum efficiency at 365 nm: 16.4%). Theoretical calculations reveal that interactions of Cu nanoclusters with TiO2 could affect their electronic structures, leading to higher adsorption energy of CH3OH at Ti sites and a lower barrier for the dehydrogenation of CH3OH by the synergistic effect of Cu nanoclusters and TiO2, and lower Gibbs free energy for desorption HCHO and H-2 as well.
引用
收藏
页码:18619 / 18626
页数:8
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