Elucidation of a Core–Shell Structure in Phenyl-Grafted Carbon Nitride/TiO 2 Nanohybrids for Visible-Light-Mediated H 2 Production with Simultaneous Rhodamine B Degradation
Source abstract
Abstract
Dual-functional photocatalysts help to maximize resource utilization in water remediation, but often they are visible-light-inactive, toxic, and cost-intensive. Herein, a type-II heterojunction visible-light-active photocatalyst is reported for tandem degradation of Rhodamine B and generation of H 2 . A Rhodamine B degradation rate of 2.3 × 10 –2 min –1 and H 2 production activity of 5789 μmol h –1 g –1 are shown. The hybrid shows a gradient core–shell morphology with a visible - light-absorbing phenyl-modified carbon nitride (PhCN) core and a porous PhCN/TiO 2 outer shell, resulting in an enhanced interaction between the catalyst and the surroundings. The nanoscale crystallization of TiO 2 on PhCN’s surface, shifts the triazine network structure, while autoclave treatments further increase the band gap and suppress charge carrier recombination. The influence of nanoscale morphological changes on photocatalytic activity was examined by varying the component ratios and thermal treatments, highlighting the strong correlation between the nanoscale architecture and the enhanced catalytic activity. This work provides a detailed guide to the exploration of environmentally friendly dual-functional photocatalysts.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Advanced Photocatalysis Techniques · Advanced Nanomaterials in Catalysis · Covalent Organic Framework Applications
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Department of Physics, University of Cagliari, Complesso Universitario di Monserrato S.P. Monserrato-Sestu Km 0, 700 09042 Monserrato (CA), Italy
TU Wien, Institute of Materials Chemistry, Division Molecular Materials Chemistry, Getreidemarkt 9/BC/02, 1060 Vienna, Austria
Funding
Erasmus+ · Austrian Science Fund · Royal Society of Chemistry · Ministero dell'Universit? e della Ricerca
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