Coupling photocatalytic CO 2 reduction and CH 3 OH oxidation for selective dimethoxymethane production.
Yixuan WangYang LiuLingling WangSilambarasan PerumalHongdan WangHyun KoChung Li DongPanpan ZhangShuaijun WangTa Thi Thuy NgaYoung Dok KimYujing JiShufang ZhaoJi-Hee KimDong-Yub YeeYosep HwangJinqiang ZhangMin Gyu KimHyoyoung LeePublished in: Nature communications (2024)
Currently, conventional dimethoxymethane synthesis methods are environmentally unfriendly. Here, we report a photo-redox catalysis system to generate dimethoxymethane using a silver and tungsten co-modified blue titanium dioxide catalyst (Ag.W-BTO) by coupling CO 2 reduction and CH 3 OH oxidation under mild conditions. The Ag.W-BTO structure and its electron and hole transfer are comprehensively investigated by combining advanced characterizations and theoretical studies. Strikingly, Ag.W-BTO achieve a record photocatalytic activity of 5702.49 µmol g -1 with 92.08% dimethoxymethane selectivity in 9 h of ultraviolet-visible irradiation without sacrificial agents. Systematic isotope labeling experiments, in-situ diffuse reflectance infrared Fourier-transform analysis, and theoretical calculations reveal that the Ag and W species respectively catalyze CO 2 conversion to *CH 2 O and CH 3 OH oxidation to *CH 3 O. Subsequently, an asymmetric carbon-oxygen coupling process between these two crucial intermediates produces dimethoxymethane. This work presents a CO 2 photocatalytic reduction system for multi-carbon production to meet the objectives of sustainable economic development and carbon neutrality.
Keyphrases
- visible light
- room temperature
- electron transfer
- ionic liquid
- highly efficient
- gold nanoparticles
- molecular dynamics
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- radiation therapy
- genome wide
- density functional theory
- single cell
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- gene expression
- hydrogen peroxide
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- mass spectrometry
- radiation induced
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