The Role of Single Copper Atoms in Enhancing the Photocatalytic Activity of Carbon Nitride for Selective Oxidation

Full item record

dc.contributor.authorSudrajat, Hanggara
dc.contributor.authorPhanthuwongpakdee, Jakkapon
dc.contributor.authorColmenares, Juan Carlos
dc.contributor.organizationInstitute of Physical Chemistry, Polish Academy of Sciences
dc.contributor.organizationQuantum Materials Group, Research Center for Quantum Physics, National Research and Innovation Agency (BRIN), South Tangerang, Indonesia
dc.contributor.organizationCollaboration Research Center for Advanced Energy Materials, BRIN – Institut Teknologi Bandung, Bandung, Indonesia
dc.contributor.organizationFaculty of Environment and Resource Studies, Mahidol University, Nakhon Pathom, Thailand
dc.date.accessioned2025-05-13T13:34:00Z
dc.date.available2025-05-13T13:34:00Z
dc.date.issued2025
dc.description.abstractPhotocatalytic reactions are driven by excited charge carriers; therefore, their performance inherentlyndepends on photocarrier behavior. In this study, we examine the relationship between photocarriernbehavior and the photocatalytic activity of g-C₃N₄ loaded with single Cu atoms for the selectivenoxidation in water. As probed with transient microwave conductivity, the introduction of single Cu atoms enhances photoconductivity by increasing the mobility and extending the lifetimes of photoexcited electrons. This enhancement results in a greater population of mobile electrons. While pristine g-C₃N₄ exhibits no measurable photoconductivity, it is still capable of driving photocatalytic reactions. This suggests that in g-C₃N₄, photoexcited electrons are predominantly trapped rather than recombined, yet they are sufficiently reactive. The product of photoconductivity and electron lifetime shows a linear correlation with photocatalytic activity, demonstrating its potential as a promising descriptor for catalyst design. In terms of performance, our photocatalysts achieve a yield-to-power ratio of up to 1.1 mmol g⁻¹ h⁻¹ W⁻¹ for benzaldehyde production from benzyl alcohol under 455 nm irradiation with 100% selectivity and aromatic balance and an apparent quantum yield of 0.82%. The reaction proceeds under ambient conditions without the need for additives or external oxidants. Equally important, H₂O₂ is also produced at a rate as high as 0.26 mmol g⁻¹ h⁻¹.en
dc.identifier.citationMater. Chem. Front., 2025, Accepted
dc.identifier.issn2052-1537
dc.identifier.urihttps://open.icm.edu.pl/handle/123456789/25833
dc.language.isoen
dc.publisherRoyal Society of Chemistry
dc.relation.urihttps://doi.org/10.18150/CS0EKV
dc.rightsUznanie autorstwa 4.0 Międzynarodoween
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.sourceMaterials Chemistry Frontiers
dc.subjectphotocatalysisen
dc.titleThe Role of Single Copper Atoms in Enhancing the Photocatalytic Activity of Carbon Nitride for Selective Oxidationen
dc.typearticle
dc.type.versionacceptedVersion
person.identifier.orcidSudrajat, Hanggara [0000-0002-2720-0569]
Files for this record
Original bundle
Now showing 1 - 1 of 1
Name: Preprint_Mater Chem Front.pdf
Size: 1.87 MB
Format: Adobe Portable Document Format
Description:
License files
Name: license_rdf
Size: 1019 B
Format: RDF serialized in XML
Description: