Institutional Repository

Charge Redistribution in Nise₂/Mos₂ n–n Heterojunction Towards the Photoelectrocatalytic Degradation of Ciprofloxacin

Show simple item record

dc.contributor.author Yusuf, Tunde L.
dc.contributor.author Olatunde, Olalekan C.
dc.contributor.author Masekela, Daniel
dc.contributor.author Modibane, Kwena D.
dc.contributor.author Onwudiwe, Damian C.
dc.contributor.author Makgato, Seshibe
dc.date.accessioned 2024-08-20T15:05:28Z
dc.date.available 2024-08-20T15:05:28Z
dc.date.issued 2024-07-25
dc.identifier.citation Tunde L. Yusuf, Olalekan C. Olatunde, Daniel Masekela, Kwena D. Modibane, Damian C. Onwudiwe, Seshibe Makgato, Charge Redistribution in Nise2/Mos2 n–n Heterojunction towards the Photoelectrocatalytic Degradation of Ciprofloxacin, 2024, https://doi.org/10.1002/celc.202400309. en
dc.identifier.issn 2196-0216
dc.identifier.uri doi.org/10.1002/celc.202400309
dc.identifier.uri https://hdl.handle.net/10500/31511
dc.description.abstract This study reports the photoelectrocatalytic (PEC) activity of a n–n heterojunction comprising MoS2 and NiSe2. The synthesis of the composite was achieved through a facile solvothermal method, yielding an exfoliated MoS2 layered sheet loaded with NiSe2 nanoparticles. Under visible light radiation and an external electric field, the obtained composite NiSe2/MoS2 exhibited enhanced catalytic activity for ciprofloxacin (CIP) degradation. The NiSe2/MoS2 heterojunction achieved about 78% degradation efficiency with a first-order kinetic rate of 0.0111 min-1, compared to 38% efficiency and a first-order kinetic rate of 0.0044 min-1, observed for MoS2. The NiSe2/MoS2 heterojunction was more advantageous due to the synergy of charge carrier induction by visible light radiation and improved charge carrier separation induced by the external electric field. The formation of n–n heterojunction at the interface of the two materials resulted in charge redistribution in the materials, with a simultaneous realignment of the band structure to achieve Fermi energy equilibration. The primary reactive species responsible for CIP degradation was identified as the photo-induced h+. Furthermore, the catalyst exhibited high stability and reusability, with no significant reduction in activity observed after five experimental cycles. This study reveals the potential of exploring the synergy between the photocatalytic and electrocatalytic processes in removing harmful pharmaceutical compounds from water. en
dc.language.iso en en
dc.publisher Wiley-VCH GmbH en
dc.title Charge Redistribution in Nise₂/Mos₂ n–n Heterojunction Towards the Photoelectrocatalytic Degradation of Ciprofloxacin en
dc.type Article en


Files in this item

This item appears in the following Collection(s)

Show simple item record

Search UnisaIR


Browse

My Account

Statistics