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Title Enhancing deep visible-light photoelectrocatalysis with a single solid-state synthesis: Carbon nitride/TiO2 heterointerface
ID_Doc 7849
Authors Silva, IF; Pulignani, C; Odutola, J; Galushchinskiy, A; Texeira, IF; Isaacs, M; Mesa, CA; Scoppola, E; These, A; Badamdorj, B; Muñoz-Márquez, MA; Zizak, I; Palgrave, R; Tarakina, NV; Gimenez, S; Brabec, C; Bachmann, J; Cortes, E; Tkachenko, N; Savateev, O; Jiménez-Calvo, P
Title Enhancing deep visible-light photoelectrocatalysis with a single solid-state synthesis: Carbon nitride/TiO2 heterointerface
Year 2025
Published
DOI 10.1016/j.jcis.2024.09.028
Abstract Visible-light responsive, stable, and abundant absorbers are required for the rapid integration of green, clean, and renewable technologies in a circular economy. Photoactive solid-solid heterojunctions enable multiple charge pathways, inhibiting recombination through efficient charge transfer across the interface. This study spotlights the physico-chemical synergy between titanium dioxide (TiO2) anatase and carbon nitride (CN) to form a hybrid material. The CN(10%)-TiO2(90%) hybrid outperforms TiO2 and CN references and literature homologs in four photo and photoelectrocatalytic reactions. CN-TiO2 achieved a four-fold increase in benzylamine conversion, with photooxidation conversion rates of 51, 97, and 100 % at 625, 535, and 465 nm, respectively. The associated energy transfer mechanism was elucidated. In photoelectrochemistry, CN-TiO2 exhibited 23 % photoactivity of the full-spectrum measurement when using a 410 nm filter. Our findings demonstrate that CN-TiO2 displayed a band gap of 2.9 eV, evidencing TiO2 photosensitization attributed to enhanced charge transfer at the heterointerface boundaries via staggered heterojunction type II.
Author Keywords TiO2 sensitization; Heterointerface; CN-TiO2 composite; Benzylamine photooxidation; Hydrogen production
Index Keywords Index Keywords
Document Type Other
Open Access Open Access
Source Science Citation Index Expanded (SCI-EXPANDED)
EID WOS:001312570100001
WoS Category Chemistry, Physical
Research Area Chemistry
PDF https://doi.org/10.1016/j.jcis.2024.09.028
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