中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
Interfacial Fe5C2-Cu catalysts toward low-pressure syngas conversion to long-chain alcohols

文献类型:期刊论文

作者Li, Yinwen7; Gao, Wa1,2,4; Peng, Mi1,2,4; Zhang, Junbo7; Sun, Jialve7; Xu, Yao1,2,4; Hong, Song7; Liu, Xi3,5; Liu, Xingwu3,5; Wei, Min7
刊名NATURE COMMUNICATIONS
出版日期2020-01-03
卷号11期号:1页码:8
ISSN号2041-1723
DOI10.1038/s41467-019-13691-4
通讯作者Wei, Min(weimin@mail.buct.edu.cn) ; Zhang, Bingsen(bszhang@imr.ac.cn) ; Ma, Ding(dma@pku.edu.cn)
英文摘要Long-chain alcohols synthesis (LAS, C5+OH) from syngas provides a promising route for the conversion of coal/biomass/natural gas into high-value chemicals. Cu-Fe binary catalysts, with the merits of cost effectiveness and high CO conversion, have attracted considerable attention. Here we report a nano-construct of a Fe5C2-Cu interfacial catalyst derived from Cu4Fe1Mg4-layered double hydroxide (Cu4Fe1Mg4-LDH) precursor, i.e., Fe5C2 clusters (similar to 2 nm) are immobilized onto the surface of Cu nanoparticles (similar to 25 nm). The interfacial catalyst exhibits a CO conversion of 53.2%, a selectivity of 14.8 mol% and a space time yield of 0.101 g g(cat)(-1) h(-1) for long-chain alcohols, with a surprisingly benign reaction pressure of 1 MPa. This catalytic performance, to the best of our knowledge, is comparable to the optimal level of Cu-Fe catalysts operated at much higher pressure (normally above 3 MPa).
资助项目National Natural Science Foundation of China[NSFC: 21871021] ; National Natural Science Foundation of China[21521005] ; National Natural Science Foundation of China[21725301] ; National Natural Science Foundation of China[21932002] ; National Natural Science Foundation of China[21821004] ; National Natural Science Foundation of China[91645115] ; National Key Research and Development Program[2017YFA0206804] ; National Key Research and Development Program[2017YFB0602200] ; Fundamental Research Funds for the Central Universities[XK1802-6] ; Fundamental Research Funds for the Central Universities[buctylkxj01]
WOS研究方向Science & Technology - Other Topics
语种英语
出版者NATURE PUBLISHING GROUP
WOS记录号WOS:000551405900001
资助机构National Natural Science Foundation of China ; National Key Research and Development Program ; Fundamental Research Funds for the Central Universities
源URL[http://ir.imr.ac.cn/handle/321006/139945]  
专题金属研究所_中国科学院金属研究所
通讯作者Wei, Min; Zhang, Bingsen; Ma, Ding
作者单位1.Peking Univ, Coll Chem & Mol Engn, Beijing Natl Lab Mol Sci, Beijing 100871, Peoples R China
2.Peking Univ, Coll Engn, Beijing 100871, Peoples R China
3.Chinese Acad Sci Taiyuan, Inst Coal Chem, State Key Lab Coal Convers, Taiyuan 030001, Shanxi, Peoples R China
4.Peking Univ, BIC ESAT, Beijing 100871, Peoples R China
5.Synfuels China Beijing, Beijing 100195, Peoples R China
6.Chinese Acad Sci, Inst Met Res, Shenyang Natl Lab, Beijing 100871, Peoples R China
7.Beijing Univ Chem Technol, Beijing Adv Innovat Ctr Soft Matter Sci & Engn, State Key Lab Chem Resource Engn, Beijing 100029, Peoples R China
推荐引用方式
GB/T 7714
Li, Yinwen,Gao, Wa,Peng, Mi,et al. Interfacial Fe5C2-Cu catalysts toward low-pressure syngas conversion to long-chain alcohols[J]. NATURE COMMUNICATIONS,2020,11(1):8.
APA Li, Yinwen.,Gao, Wa.,Peng, Mi.,Zhang, Junbo.,Sun, Jialve.,...&Ma, Ding.(2020).Interfacial Fe5C2-Cu catalysts toward low-pressure syngas conversion to long-chain alcohols.NATURE COMMUNICATIONS,11(1),8.
MLA Li, Yinwen,et al."Interfacial Fe5C2-Cu catalysts toward low-pressure syngas conversion to long-chain alcohols".NATURE COMMUNICATIONS 11.1(2020):8.

入库方式: OAI收割

来源:金属研究所

浏览0
下载0
收藏0
其他版本

除非特别说明,本系统中所有内容都受版权保护,并保留所有权利。