Porous Graphene-Confined Fe-K as Highly Efficient Catalyst for CO2 Direct Hydrogenation to Light Olefins

被引:120
|
作者
Wu, Tijun [1 ,2 ]
Lin, Jun [3 ]
Cheng, Yi [1 ,2 ]
Tian, Jing [1 ,2 ]
Wang, Shunwu [1 ,2 ]
Xie, Songhai [1 ,2 ]
Pei, Yan [1 ,2 ]
Yan, Shirun [1 ,2 ]
Qiao, Minghua [1 ,2 ]
Xu, Hualong [1 ,2 ]
Zong, Baoning [4 ]
机构
[1] Fudan Univ, Collaborat Innovat Ctr Chem Energy Mat, Dept Chem, Shanghai 200433, Peoples R China
[2] Fudan Univ, Shanghai Key Lab Mol Catalysis & Innovat Mat, Shanghai 200433, Peoples R China
[3] Chinese Acad Sci, Shanghai Inst Appl Phys, Key Lab Nucl Anal Tech, Shanghai 201800, Peoples R China
[4] SINOPEC, Res Inst Petr Proc, State Key Lab Catalyt Mat & Chem Engn, Beijing 100083, Peoples R China
基金
中国国家自然科学基金; 国家重点研发计划;
关键词
porous graphene; potassium-promoted iron; CO2; hydrogenation; light olefins; FISCHER-TROPSCH SYNTHESIS; CARBON-DIOXIDE; IRON CATALYSTS; REDUCTION; CONVERSION; STRATEGIES; ENERGY; FUELS;
D O I
10.1021/acsami.8b05411
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
We devised iron-based catalysts with honeycomb structured graphene (HSG) as the support and potassium as the promoter for CO2 direct hydrogenation to light olefins (CO2-FTO). Over the optimal FeK1.5/HSG catalyst, the iron time yield of light olefins amounted to 73 mu mol(CO2) g(Fe)(-1) s(-1) with high selectivity of 59%. No obvious deactivation occurred within 120 h on stream. The excellent catalytic performance is attributed to the confinement effect of the porous HSG on the sintering of the active sites and the promotion effect of potassium on the activation of inert CO2 and the formation of iron carbide active for CO2-FTO.
引用
收藏
页码:23439 / 23443
页数:5
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