Direct Conversion of CO<sub>2</sub> to Ethanol Boosted by Intimacy-Sensitive Multifunctional Catalysts
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- Yang Wang
- Institute of New Energy, College of New Energy, State Key Laboratory of Heavy Oil Processing, China University of Petroleum (East China), Qingdao 266580, China
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- Kangzhou Wang
- Department of Applied Chemistry, Graduate School of Engineering, University of Toyama, Gofuku 3190, Toyama 930-8555, Japan
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- Baizhang Zhang
- Department of Applied Chemistry, Graduate School of Engineering, University of Toyama, Gofuku 3190, Toyama 930-8555, Japan
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- Xiaobo Peng
- Department of Applied Chemistry, Graduate School of Engineering, University of Toyama, Gofuku 3190, Toyama 930-8555, Japan
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- Xinhua Gao
- State Key Laboratory of High-Efficiency Utilization of Coal and Green Chemical Engineering, College of Chemistry & Chemical Engineering, Ningxia University, Yinchuan 750021, China
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- Guohui Yang
- Department of Applied Chemistry, Graduate School of Engineering, University of Toyama, Gofuku 3190, Toyama 930-8555, Japan
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- Han Hu
- Institute of New Energy, College of New Energy, State Key Laboratory of Heavy Oil Processing, China University of Petroleum (East China), Qingdao 266580, China
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- Mingbo Wu
- Institute of New Energy, College of New Energy, State Key Laboratory of Heavy Oil Processing, China University of Petroleum (East China), Qingdao 266580, China
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- Noritatsu Tsubaki
- Department of Applied Chemistry, Graduate School of Engineering, University of Toyama, Gofuku 3190, Toyama 930-8555, Japan
説明
It is still a challenge to realize highly efficient conversion of CO 2 to a single target chemical. Herein, substantial progress has been made, both in catalyst design and reaction route exploration, for the direct conversion of CO 2 to ethanol. An alkene synthesis Na-Fe@C catalyst was integrated with another potassium-doped methanol synthesis CuZnAl catalyst to realize the direct conversion of CO 2 (39.2%) to ethanol (35.0%) selectively, accompanied by some useful alkene formation (33.0%). More in-depth in situ characterizations and density functional theory (DFT) calculations suggested that the unique catalytic interfaces, intimacy modes of the multifunctional catalysts, as well as the intermediate of aldehyde species played vital roles in the higher conversion rate of CO 2 to ethanol. Moreover, the multifunctional catalyst is easy to fabricate, regenerate, and recycle, being very close to the real industry application. Therefore, this work is promising to enrich the horizon of the economical utilization of CO 2 for renewable chemical synthesis.
収録刊行物
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- ACS Catalysis
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ACS Catalysis 11 (18), 11742-11753, 2021-09-07
American Chemical Society (ACS)
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キーワード
- Chemical Sciences not elsewhere classified
- higher conversion rate
- another potassium
- Biochemistry
- real industry application
- sensitive multifunctional catalysts
- Sociology
- multifunctional catalysts
- alkene synthesis na
- multifunctional catalyst
- direct conversion
- economical utilization
- calculations suggested
- density functional theory
- renewable chemical synthesis
- c catalyst
- 660
- 0 %) selectively
- 540
- situ </
- 2 %)
- single target chemical
- 0 %)
- 2 </ sub
- substantial progress
- catalyst design
- reaction route exploration
- useful alkene formation
- unique catalytic interfaces
- Biotechnology
詳細情報 詳細情報について
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- CRID
- 1360013168845268480
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- ISSN
- 21555435
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- 資料種別
- journal article
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- データソース種別
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- Crossref
- KAKEN
- OpenAIRE
