Repository logoGCRIS
  • English
  • Türkçe
  • Русский
Log In
New user? Click here to register. Have you forgotten your password?
Home
Communities
Browse GCRIS
Entities
Overview
GCRIS Guide
  1. Home
  2. Browse by Author

Browsing by Author "Kuru, Talha"

Filter results by typing the first few letters
Now showing 1 - 2 of 2
  • Results Per Page
  • Sort Options
  • Loading...
    Thumbnail Image
    Article
    Citation - WoS: 2
    Citation - Scopus: 4
    Dye-Sensitized Sepiolite Clay as Natural Scaffolds for Visible Light Driven Photocatalytic Hydrogen Evolution
    (Pergamon-Elsevier Science Ltd, 2025) Acar, Eminegul Genc; Akyildiz, Yigit Osman; Kuru, Talha; Yenel, Esma; Aslan, Emre; Ersoz, Mustafa; Patir, Hatay
    Natural clay minerals are increasingly used as superior support materials for various photocatalysts due to their excellent adsorption capacity, negative surface charge, suitable thermal/chemical stability, large specific surface area, and strong surface reactivity, resulting in low agglomeration and suppression of charge recombination. However, they are still insufficient for photocatalysis due to their low efficiency. Therefore, sensitization of clay minerals with dyes to improve the efficiency and specificity of catalysts is considered a promising route for photocatalytic applications. In this work, the effect of dye sensitization on visible light-driven photocatalytic water splitting of microfibrous sepiolite scaffolds as natural photocatalyst supports was investigated for the first time by using various xanthene dyes (eosin Y, rhodamine B and eryhtrosine B (ErB)) and triethanolamine as photosensitizers and sacrificial agents, respectively, in the absence and presence of platinum as a co-catalyst. The clay/dye system was characterized using various techniques such as X-ray photoelectron spectroscopy, transmission electron microscopy, scanning electron microscopy and energy dispersive X-rays. Sep/ErB photocatalysts produced the highest amount of hydrogen among the other Sep/dye scaffold systems because they act as an effective matrix by preventing nanoparticle aggregation and promoting electron transfer due to their excellent crystal structures and physicochemical properties.
  • Loading...
    Thumbnail Image
    Article
    Citation - WoS: 12
    Citation - Scopus: 13
    Photodeposition of Molybdenum Sulfide on Mtio3 (m: Ba, Sr) Perovskites for Photocatalytic Hydrogen Evolution
    (Elsevier Science Sa, 2023) Kuru, Talha; Yanalak, Gizem; Sarilmaz, Adem; Aslan, Emre; Keles, Ali; Genç, Munevver Tuna; Özel, Faruk
    Photocatalytic hydrogen evolution using by semiconductor materials have been studied effectively by converting solar energy into the chemical energy. Perovskite-based materials have been widely used as semiconductor catalysts for the photocatalytic hydrogen production. Herein, molybdenum sulfide photodeposited onto MTiO3 (M: Ba, Sr) perovskites (MTiO3/MoSx) have been investigated on the photocatalytic hydrogen evolution under solar light irradiation in the presence of triethanolamine (TEOA) and eosin Y (EY) as an electron donor and photosensitizer, respectively. Compared to pristine MTiO3, BaTiO3/MoSx and SrTiO3/MoSx show a remarkable improvement in the hydrogen production efficiency and stability. Photocatalytic hydrogen evolution activities found in the order of SrTiO3/MoSx > BaTiO3/MoSx > MoSx > SrTiO3 > BaTiO3. In addition, photocatalytic hydrogen activity of SrTiO3/Pt was evaluated for comparison with SrTiO3/MoSx under the same conditions and SrTiO3/MoSx produced higher hydrogen activity than SrTiO3/Pt due to the high active sites created by MoSx on the catalyst surface which is originated from Mo-S and S-S bonds.
Repository logo
Collections
  • Scopus Collection
  • WoS Collection
  • TrDizin Collection
  • PubMed Collection
Entities
  • Research Outputs
  • Organizations
  • Researchers
  • Projects
  • Awards
  • Equipments
  • Events
About
  • Contact
  • GCRIS
  • Research Ecosystems
  • Feedback
  • OAI-PMH

Log in to GCRIS Dashboard

Powered by Research Ecosystems

  • Privacy policy
  • End User Agreement
  • Feedback