CO2 Hydrogenation over Copper/ZnO Single-Atom Catalysts: Water-Promoted Transient Synthesis of Methanol

被引:51
|
作者
Wu, Wenlong [1 ]
Wang, Yanan [1 ,2 ,3 ,4 ]
Luo, Lei [1 ]
Wang, Menglin [1 ]
Li, Zhongling [1 ]
Chen, Yue [1 ]
Wang, Zhiqi [1 ]
Chai, Jingbo [1 ]
Cen, Zeyan [1 ]
Shi, Yongliang [1 ,5 ]
Zhao, Jin [1 ]
Zeng, Jie [1 ]
Li, Hongliang [1 ]
机构
[1] Univ Sci & Technol China, Dept Phys,Hefei Natl Res Ctr Phys Sci & Microscal, Dept Chem Phys,CAS Key Lab Strongly Coupled Quant, Natl Synchrotron Radiat Lab,Key Lab Surface & Int, Hefei 230026, Anhui, Peoples R China
[2] Songshan Lake Mat Lab, Dongguan 523808, Guangdong, Peoples R China
[3] Chinese Acad Sci, Beijing Natl Lab Condensed Matter Phys, Beijing 100190, Peoples R China
[4] Chinese Acad Sci, Inst Phys, Beijing 100190, Peoples R China
[5] Xian Jiaotong Univ Xian, Ctr Spintron & Quantum Syst, Sch Mat Sci & Engn, State Key Lab Mech Behav Mat, Xian 710049, Shanxi, Peoples R China
基金
中国博士后科学基金;
关键词
CO2; Cu; ZnO; Methanol; Single-Atom Catalysis; Water; LEVEL;
D O I
10.1002/anie.202213024
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The hydrogenation of CO2 by renewable power-generated hydrogen offers a promising approach to a sustainable carbon cycle. However, the role of water during CO2 hydrogenation is still under debate. Herein, we demonstrated that either too low or too high contents of water hampered the methanol synthesis over Cu/ZnO based catalysts. For Cu single atoms on ZnO supports, the optimal content of water was 0.11 vol. % under 30 bar (CO2 : H-2=1 : 3) at 170 degrees C. Upon the introduction of optimal-content water, the methanol selectivity immediately became 99.1 %, meanwhile the conversion of CO2 underwent a volcano-type trend with the maximum of 4.9 %. According to mechanistic studies, water acted as a bridge between H atoms and CO2/intermediates, facilitating the transformation of COOH* and CH2O*. The enhanced activity induced the generation of more water to react with CO via water-gas shift reaction, resulting in the increase in methanol selectivity.
引用
收藏
页数:8
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