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Homogeneous and heterogeneous catalysts for hydrogenation of CO2 to methanol under mild conditions
Bai, Shao-Tao1; De Smet, Gilles2; Liao, Yuhe1,4; Sun, Ruiyan1; Zhou, Cheng1; Beller, Matthias3; Maes, Bert U. W.2; Sels, Bert F.1
2021-04-07
Source PublicationCHEMICAL SOCIETY REVIEWS
ISSN0306-0012
Volume50Issue:7Pages:4259-4298
Corresponding AuthorBeller, Matthias(Matthias.Beller@catalysis.de) ; Maes, Bert U. W.(bert.maes@uantwerpen.be) ; Sels, Bert F.(bert.sels@kuleuven.be)
AbstractIn the context of a carbon neutral economy, catalytic CO2 hydrogenation to methanol is one crucial technology for CO2 mitigation providing solutions for manufacturing future fuels, chemicals, and materials. However, most of the presently known catalyst systems are used at temperatures over 220 degrees C, which limits the theoretical yield of methanol production due to the exothermic nature of this transformation. In this review, we summarize state-of-the-art catalysts, focusing on the rationales behind, for CO2 hydrogenation to methanol at temperatures lower than 170 degrees C. Both hydrogenation with homogeneous and heterogeneous catalysts is covered. Typically, additives (alcohols, amines or aminoalcohols) are used to transform CO2 into intermediates, which can further be reduced into methanol. In the first part, molecular catalysts are discussed, organized into: (1) monofunctional, (2) M/NH bifunctional, and (3) aromatization-dearomatization bifunctional molecular catalysts. In the second part, heterogeneous catalysts are elaborated, organized into: (1) metal/metal or metal/support, (2) active-site/N or active-site/OH bifunctional heterogeneous catalysts, and (3) cooperation of catalysts and additives in a tandem process via crucial intermediates. Although many insights have been gained in this transformation, in particular for molecular catalysts, the mechanisms in the presence of heterogeneous catalysts remain descriptive and insights unclear.
DOI10.1039/d0cs01331e
WOS KeywordMETAL-LIGAND COOPERATION ; TETRADENTATE BIPYRIDINE LIGANDS ; LOW-TEMPERATURE HYDROGENATION ; CARBON-DIOXIDE ; ASYMMETRIC HYDROGENATION ; CARBOXYLIC-ACIDS ; FORMIC-ACID ; NONCOVALENT INTERACTIONS ; SEQUENTIAL HYDROGENATION ; 5-CO-ORDINATE COMPLEXES
Indexed BySCI
Language英语
Funding ProjectFederal Excellence of Science (EoS) call of FWO/FNRS (BIOFACT)[30902231] ; European Research Council (ERC)[NoNaCat 670986] ; KU Leuven ; special research fund BOF UAntwerpen
WOS Research AreaChemistry
Funding OrganizationFederal Excellence of Science (EoS) call of FWO/FNRS (BIOFACT) ; European Research Council (ERC) ; KU Leuven ; special research fund BOF UAntwerpen
WOS SubjectChemistry, Multidisciplinary
WOS IDWOS:000639924700015
PublisherROYAL SOC CHEMISTRY
Citation statistics
Cited Times:174[WOS]   [WOS Record]     [Related Records in WOS]
Document Type期刊论文
Identifierhttp://ir.giec.ac.cn/handle/344007/33176
Collection中国科学院广州能源研究所
Corresponding AuthorBeller, Matthias; Maes, Bert U. W.; Sels, Bert F.
Affiliation1.Katholieke Univ Leuven, Ctr Sustainable Catalysis & Engn, Celestijnenlaan 200F, B-3001 Heverlee, Belgium
2.Univ Antwerp, Dept Chem, Div Organ Synth, Groenenborgerlaan 171, B-2020 Antwerp, Belgium
3.Leibniz Inst Catalysis, Albert Einstein Str 29a, Rostock, Germany
4.Chinese Acad Sci, Guangzhou Inst Energy Convers, Guangzhou 510640, Peoples R China
Recommended Citation
GB/T 7714
Bai, Shao-Tao,De Smet, Gilles,Liao, Yuhe,et al. Homogeneous and heterogeneous catalysts for hydrogenation of CO2 to methanol under mild conditions[J]. CHEMICAL SOCIETY REVIEWS,2021,50(7):4259-4298.
APA Bai, Shao-Tao.,De Smet, Gilles.,Liao, Yuhe.,Sun, Ruiyan.,Zhou, Cheng.,...&Sels, Bert F..(2021).Homogeneous and heterogeneous catalysts for hydrogenation of CO2 to methanol under mild conditions.CHEMICAL SOCIETY REVIEWS,50(7),4259-4298.
MLA Bai, Shao-Tao,et al."Homogeneous and heterogeneous catalysts for hydrogenation of CO2 to methanol under mild conditions".CHEMICAL SOCIETY REVIEWS 50.7(2021):4259-4298.
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