共 28 条
Oxygen vacancy promoted carbon dioxide activation over Cu/ZrO2 for CO2-to-methanol conversion
被引:20
作者:

Chang, Haohao
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Fudan Univ, Dept Chem, Shanghai Key Lab Mol Catalysis & Innovat Mat, Shanghai 200433, Peoples R China Fudan Univ, Dept Chem, Shanghai Key Lab Mol Catalysis & Innovat Mat, Shanghai 200433, Peoples R China

Gao, Feifan
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Fudan Univ, Dept Chem, Shanghai Key Lab Mol Catalysis & Innovat Mat, Shanghai 200433, Peoples R China Fudan Univ, Dept Chem, Shanghai Key Lab Mol Catalysis & Innovat Mat, Shanghai 200433, Peoples R China

Luo, Alin
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Fudan Univ, Dept Chem, Shanghai Key Lab Mol Catalysis & Innovat Mat, Shanghai 200433, Peoples R China Fudan Univ, Dept Chem, Shanghai Key Lab Mol Catalysis & Innovat Mat, Shanghai 200433, Peoples R China

Liu, Yongmei
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h-index: 0
机构:
Fudan Univ, Dept Chem, Shanghai Key Lab Mol Catalysis & Innovat Mat, Shanghai 200433, Peoples R China Fudan Univ, Dept Chem, Shanghai Key Lab Mol Catalysis & Innovat Mat, Shanghai 200433, Peoples R China

Zhu, Yifeng
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h-index: 0
机构:
Fudan Univ, Dept Chem, Shanghai Key Lab Mol Catalysis & Innovat Mat, Shanghai 200433, Peoples R China Fudan Univ, Dept Chem, Shanghai Key Lab Mol Catalysis & Innovat Mat, Shanghai 200433, Peoples R China

He, Heyong
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机构:
Fudan Univ, Dept Chem, Shanghai Key Lab Mol Catalysis & Innovat Mat, Shanghai 200433, Peoples R China Fudan Univ, Dept Chem, Shanghai Key Lab Mol Catalysis & Innovat Mat, Shanghai 200433, Peoples R China

Cao, Yong
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h-index: 0
机构:
Fudan Univ, Dept Chem, Shanghai Key Lab Mol Catalysis & Innovat Mat, Shanghai 200433, Peoples R China Fudan Univ, Dept Chem, Shanghai Key Lab Mol Catalysis & Innovat Mat, Shanghai 200433, Peoples R China
机构:
[1] Fudan Univ, Dept Chem, Shanghai Key Lab Mol Catalysis & Innovat Mat, Shanghai 200433, Peoples R China
基金:
国家重点研发计划;
中国国家自然科学基金;
关键词:
CO2;
HYDROGENATION;
CATALYSTS;
METHANOL;
ZIRCONIA;
ZRO2;
SURFACE;
SITES;
STATE;
D O I:
10.1039/d3cc01834b
中图分类号:
O6 [化学];
学科分类号:
0703 ;
摘要:
Oxygen vacancy-enriched ultrafine tetragonal ZrO2 was introduced as a support for copper nanoparticles to enhance the energy efficiency of CO2 hydrogenation for methanol synthesis. In situ spectroscopic techniques confirmed the oxygen vacancy-mediated single-electron CO2 activation. The resulting highly efficient catalyst yielded a methanol production rate of 550 mg g(cat)(-1) h(-1) at 200 degrees C, outperforming state-of-the-art Cu-based catalysts.
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页码:7647 / 7650
页数:4
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