File Download

There are no files associated with this item.

  • Find it @ UNIST can give you direct access to the published full text of this article. (UNISTARs only)
Related Researcher

권영국

Kwon, Youngkook
Electrochemistry Lab for Energy and Environment
Read More

Views & Downloads

Detailed Information

Cited time in webofscience Cited time in scopus
Metadata Downloads

Quadruple metal-based layered structure as the photocatalyst for conversion of carbon dioxide into a value added carbon monoxide with high selectivity and efficiency

Author(s)
Kim, Keon-HanKim, SangjunMoon, Byeong CheulChoi, Jae WonJeong, Hyung MoKwon, YoungkookKwon, SunilChoi, Hwa SeobKang, Jeung Ku
Issued Date
2017-05
DOI
10.1039/c7ta01623a
URI
https://scholarworks.unist.ac.kr/handle/201301/26562
Fulltext
https://pubs.rsc.org/en/Content/ArticleLanding/2017/TA/C7TA01623A#!divAbstract
Citation
JOURNAL OF MATERIALS CHEMISTRY A, v.5, no.18, pp.8274 - 8279
Abstract
Metal-based layered structures are promising structures for use as photocatalysts, but ones that are capable of enabling a complete conversion of carbon dioxide (CO2) into a value added carbon monoxide (CO) are still limited. In this paper, a quadruple metal-based layered structure, composed of aluminium (Al), gallium (Ga), magnesium (Mg), and nickel (Ni), is reported which allows the photocatalytic conversion of CO2 into CO with a high selectivity close to 100% in the presence of water. The shifted oxidation states on the Ni and Mg ions than bivalent states lead to an increment in electronegativity for their neighboring oxygen (O) while the Ga and Al ions maintain their trivalent states, thereby enabling the O to adsorb a high amount of CO2. Furthermore, the quadruple metal-based layered structure without any use of scavengers is proven to give an approximately two-fold increase in photocatalytic activity compared to those with bi or triple metal-based structures.
Publisher
ROYAL SOC CHEMISTRY
ISSN
2050-7488
Keyword
OXYGEN EVOLUTIONCO2OXIDEREDUCTIONWATERADSORPTIONTAKOVITEFTIR

qrcode

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