File Download

There are no files associated with this item.

  Links for fulltext
     (May Require Subscription)
Supplementary

Article: Design of sculptured SnS/g-C3N4 photocatalytic nanostructure for highly efficient and selective CO2 conversion to methane

TitleDesign of sculptured SnS/g-C3N4 photocatalytic nanostructure for highly efficient and selective CO2 conversion to methane
Authors
KeywordsCO2 conversion
g-C3N4
Photocatalysts
Sculptured thin film
Tin Sulfide
Issue Date5-May-2023
PublisherElsevier
Citation
Applied Catalysis B: Environment and Energy, 2023, v. 324 How to Cite?
Abstract

Here, we demonstrate the SnS/g-C3N4 crystallized and nanostructured photocatalysts for efficient and selective CO2 conversion to CH4 by engineered thermal evaporation and the decoration of g-C3N4 through a simple dipping method, overcoming the limitation of bulk SnS-based photocatalysts. The SnS/g-C3N4 nanostructured photocatalysts exhibit a superior methane production rate of 387.5 μmol∙m−2∙h−1 (= c.a. 122.33 μmol∙g−1∙h−1) with an apparent quantum yield of c.a. 9.7% at 520 nm with engineered lengths. Moreover, 100% selective production toward CH4 is also measured from the SnS/g-C3N4 photocatalysts, with > 10 h stable operation. These performances are, to the best of our knowledge, the highest production rate among reported photocatalytic films and metal sulfide/g-C3N4 composite-based photocatalysts. These highly improved performances are attributed to synergistic effects by the formation of nanostructured SnS/g-C3N4, exhibiting superior light absorption, higher crystallinity, Z-scheme charge transport via C-S bonding, physical advantages of the SnS nanostructure, and excellent physiochemical properties of the surfaces.


Persistent Identifierhttp://hdl.handle.net/10722/350729
ISSN
2023 Impact Factor: 20.2
2023 SCImago Journal Rankings: 5.112
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorOmr, Hossam AE-
dc.contributor.authorPutikam, Raghunath-
dc.contributor.authorHussien, Mahmoud Kamal-
dc.contributor.authorSabbah, Amr-
dc.contributor.authorLin, Tsai Yu-
dc.contributor.authorChen, Kuei Hsien-
dc.contributor.authorWu, Heng Liang-
dc.contributor.authorFeng, Shien Ping-
dc.contributor.authorLin, Ming Chang-
dc.contributor.authorLee, Hyeonseok-
dc.date.accessioned2024-11-02T00:36:14Z-
dc.date.available2024-11-02T00:36:14Z-
dc.date.issued2023-05-05-
dc.identifier.citationApplied Catalysis B: Environment and Energy, 2023, v. 324-
dc.identifier.issn0926-3373-
dc.identifier.urihttp://hdl.handle.net/10722/350729-
dc.description.abstract<p>Here, we demonstrate the SnS/g-C3N4 crystallized and nanostructured photocatalysts for efficient and selective CO2 conversion to CH4 by engineered thermal evaporation and the decoration of g-C3N4 through a simple dipping method, overcoming the limitation of bulk SnS-based photocatalysts. The SnS/g-C3N4 nanostructured photocatalysts exhibit a superior methane production rate of 387.5 μmol∙m−2∙h−1 (= c.a. 122.33 μmol∙g−1∙h−1) with an apparent quantum yield of c.a. 9.7% at 520 nm with engineered lengths. Moreover, 100% selective production toward CH4 is also measured from the SnS/g-C3N4 photocatalysts, with > 10 h stable operation. These performances are, to the best of our knowledge, the highest production rate among reported photocatalytic films and metal sulfide/g-C3N4 composite-based photocatalysts. These highly improved performances are attributed to synergistic effects by the formation of nanostructured SnS/g-C3N4, exhibiting superior light absorption, higher crystallinity, Z-scheme charge transport via C-S bonding, physical advantages of the SnS nanostructure, and excellent physiochemical properties of the surfaces.</p>-
dc.languageeng-
dc.publisherElsevier-
dc.relation.ispartofApplied Catalysis B: Environment and Energy-
dc.subjectCO2 conversion-
dc.subjectg-C3N4-
dc.subjectPhotocatalysts-
dc.subjectSculptured thin film-
dc.subjectTin Sulfide-
dc.titleDesign of sculptured SnS/g-C3N4 photocatalytic nanostructure for highly efficient and selective CO2 conversion to methane-
dc.typeArticle-
dc.identifier.doi10.1016/j.apcatb.2022.122231-
dc.identifier.scopuseid_2-s2.0-85145559008-
dc.identifier.volume324-
dc.identifier.eissn1873-3883-
dc.identifier.isiWOS:001005423600001-
dc.identifier.issnl0926-3373-

Export via OAI-PMH Interface in XML Formats


OR


Export to Other Non-XML Formats