Copper adparticle enabled selective electrosynthesis of n-propanol. Issue 1 (December 2018)
- Record Type:
- Journal Article
- Title:
- Copper adparticle enabled selective electrosynthesis of n-propanol. Issue 1 (December 2018)
- Main Title:
- Copper adparticle enabled selective electrosynthesis of n-propanol
- Authors:
- Li, Jun
Che, Fanglin
Pang, Yuanjie
Zou, Chengqin
Howe, Jane
Burdyny, Thomas
Edwards, Jonathan
Wang, Yuhang
Li, Fengwang
Wang, Ziyun
De Luna, Phil
Dinh, Cao-Thang
Zhuang, Tao-Tao
Saidaminov, Makhsud
Cheng, Shaobo
Wu, Tianpin
Finfrock, Y.
Ma, Lu
Hsieh, Shang-Hsien
Liu, Yi-Sheng
Botton, Gianluigi
Pong, Way-Faung
Du, Xiwen
Guo, Jinghua
Sham, Tsun-Kong
Sargent, Edward
Sinton, David - Abstract:
- Abstract The electrochemical reduction of carbon monoxide is a promising approach for the renewable production of carbon-based fuels and chemicals. Copper shows activity toward multi-carbon products from CO reduction, with reaction selectivity favoring two-carbon products; however, efficient conversion of CO to higher carbon products such as n-propanol, a liquid fuel, has yet to be achieved. We hypothesize that copper adparticles, possessing a high density of under-coordinated atoms, could serve as preferential sites for n-propanol formation. Density functional theory calculations suggest that copper adparticles increase CO binding energy and stabilize two-carbon intermediates, facilitating coupling between adsorbed *CO and two-carbon intermediates to form three-carbon products. We form adparticle-covered catalysts in-situ by mediating catalyst growth with strong CO chemisorption. The new catalysts exhibit an n-propanol Faradaic efficiency of 23% from CO reduction at an n-propanol partial current density of 11 mA cm−2 . Upgrading wasted carbon emissions to high-value, multi-carbon products provides an economic route to reduce carbon dioxide levels, but such conversions have proven challenging. Here, authors explore copper adparticles as highly active surfaces that convert CO to n-propanol with high selectivities.
- Is Part Of:
- Nature communications. Volume 9:Issue 1(2018)
- Journal:
- Nature communications
- Issue:
- Volume 9:Issue 1(2018)
- Issue Display:
- Volume 9, Issue 1 (2018)
- Year:
- 2018
- Volume:
- 9
- Issue:
- 1
- Issue Sort Value:
- 2018-0009-0001-0000
- Page Start:
- 1
- Page End:
- 9
- Publication Date:
- 2018-12
- Subjects:
- Biology -- Periodicals
Physical sciences -- Periodicals
505 - Journal URLs:
- http://www.nature.com/ncomms/index.html ↗
http://www.nature.com/ ↗ - DOI:
- 10.1038/s41467-018-07032-0 ↗
- Languages:
- English
- ISSNs:
- 2041-1723
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 6046.280270
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 10977.xml