中文版 | English
Title

CO2 hydrogenation to high-value products via heterogeneous catalysis

Author
Corresponding AuthorFan,Maohong
Publication Years
2019-12-01
DOI
Source Title
ISSN
2041-1723
EISSN
2041-1723
Volume10Issue:1
Abstract

Recently, carbon dioxide capture and conversion, along with hydrogen from renewable resources, provide an alternative approach to synthesis of useful fuels and chemicals. People are increasingly interested in developing innovative carbon dioxide hydrogenation catalysts, and the pace of progress in this area is accelerating. Accordingly, this perspective presents current state of the art and outlook in synthesis of light olefins, dimethyl ether, liquid fuels, and alcohols through two leading hydrogenation mechanisms: methanol reaction and Fischer-Tropsch based carbon dioxide hydrogenation. The future research directions for developing new heterogeneous catalysts with transformational technologies, including 3D printing and artificial intelligence, are provided.

URL[Source Record]
Indexed By
Language
English
Important Publications
NI Journal Papers ; ESI Highly Cited Papers ; ESI Highly Cited Papers ; ESI Highly Cited Papers ; ESI Highly Cited Papers ; ESI Highly Cited Papers ; ESI Highly Cited Papers ; ESI Highly Cited Papers ; ESI Highly Cited Papers ; ESI Highly Cited Papers ; ESI Highly Cited Papers
SUSTech Authorship
Others
WOS Research Area
Science & Technology - Other Topics
WOS Subject
Multidisciplinary Sciences
WOS Accession No
WOS:000503207700001
Publisher
Scopus EID
2-s2.0-85076454153
Data Source
Scopus
Citation statistics
Cited Times [WOS]:341
Document TypeJournal Article
Identifierhttp://kc.sustech.edu.cn/handle/2SGJ60CL/73938
DepartmentDepartment of Materials Science and Engineering
Affiliation
1.Departments of Chemical and Petroleum Engineering,University of Wyoming,Laramie,82071,United States
2.Key Laboratory of Coal to Ethylene Glycol and Its Related Technology,Fujian Institute of Research on the Structure of Matter,Chinese Academy of Sciences,Fuzhou,Fujian,350002,China
3.University of Chinese Academy of Sciences,Beijing,100049,China
4.School of Chemical Engineering,Nanjing University of Science and Technology,Nanjing,210094,China
5.Department of Chemical Engineering,Brigham Young University,Provo,330 EB,84602,United States
6.State Key Laboratory of Chemical Engineering,Department of Chemical Engineering,Tsinghua University,Beijing,100084,China
7.Departments of Civil and Environmental Engineering,Stanford University,Stanford,94305,United States
8.Department of Materials Science and Engineering,Southern University of Science and Technology,Shenzhen,518055,China
9.School of Civil and Environmental Engineering,Georgia Institute of Technology,Mason Building,Atlanta,790 Atlantic Drive,30332,United States
10.School of Energy Resources,University of Wyoming,Laramie,82071,United States
Recommended Citation
GB/T 7714
Ye,Run Ping,Ding,Jie,Gong,Weibo,et al. CO2 hydrogenation to high-value products via heterogeneous catalysis[J]. Nature Communications,2019,10(1).
APA
Ye,Run Ping.,Ding,Jie.,Gong,Weibo.,Argyle,Morris D..,Zhong,Qin.,...&Yao,Yuan Gen.(2019).CO2 hydrogenation to high-value products via heterogeneous catalysis.Nature Communications,10(1).
MLA
Ye,Run Ping,et al."CO2 hydrogenation to high-value products via heterogeneous catalysis".Nature Communications 10.1(2019).
Files in This Item:
File Name/Size DocType Version Access License
s41467-019-13638-9 ((2126KB) Open Access--View
Related Services
Recommend this item
Bookmark
Usage statistics
Export to Endnote
Export to Excel
Export to Csv
Altmetrics Score
Google Scholar
Similar articles in Google Scholar
[Ye,Run Ping]'s Articles
[Ding,Jie]'s Articles
[Gong,Weibo]'s Articles
Baidu Scholar
Similar articles in Baidu Scholar
[Ye,Run Ping]'s Articles
[Ding,Jie]'s Articles
[Gong,Weibo]'s Articles
Bing Scholar
Similar articles in Bing Scholar
[Ye,Run Ping]'s Articles
[Ding,Jie]'s Articles
[Gong,Weibo]'s Articles
Terms of Use
No data!
Social Bookmark/Share
File name: s41467-019-13638-9 (1).pdf
Format: Adobe PDF
File name: s41467-019-13638-9 (1).pdf
Format: Adobe PDF
No comment.

Items in the repository are protected by copyright, with all rights reserved, unless otherwise indicated.