Structure-dependent iron-based metal-organic frameworks for selective CO2-to-CH4 photocatalytic reduction

被引:73
作者
Dao, Xiao-Yao [1 ]
Guo, Jin-Han [1 ]
Zhang, Xiao-Yu [1 ]
Wang, Shi-Qing [1 ]
Cheng, Xiao-Mei [1 ]
Sun, Wei-Yin [1 ]
机构
[1] Nanjing Univ, Collaborat Innovat Ctr Adv Microstruct, Sch Chem & Chem Engn,State Key Lab Coordinat Chem, Coordinat Chem Inst,Nanjing Natl Lab Microstruct, Nanjing 210023, Peoples R China
关键词
CARBON-DIOXIDE REDUCTION; FE-BASED MOFS; CO2; REDUCTION; ULTRASOFT PSEUDOPOTENTIALS; UNSATURATED SITES; WATER OXIDATION; LIGHT; CONVERSION; PHOTOREDUCTION; CH4;
D O I
10.1039/d0ta10278d
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Visible-light driven reduction of carbon dioxide (CO2) to methane (CH4) is a challenge in the photocatalytic reaction system. Herein, two Fe-based metal-organic frameworks (MOFs) MIL-100(Fe) and MIL-101(Fe) with single-trimetallic clusters but distinct organic ligands were employed to explore the structure-dependent CO2 conversion performance. Compared with MIL-101(Fe), MIL-100(Fe) exhibits superior catalytic activity and selectivity for CH4 generation under visible-light irradiation via a solvent-free route. This is the first report that MIL-100(Fe) finishes the photoreduction of CO2 into CH4. Importantly, the plausible conversion pathways of the reaction were given by density functional theory (DFT) calculations. This work furnishes new direction for constructing MOFs to achieve CO2-to-CH4 conversion.
引用
收藏
页码:25850 / 25856
页数:7
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