z-logo
Premium
Highly Efficient UV–Visible Photocatalyst from Monolithic 3D Titania/Graphene Quantum Dot Heterostructure Linked by Aminosilane
Author(s) -
Yoon Hyewon,
Lee Kisung,
Kim Hyojung,
Park Minsu,
Novak Travis G.,
Hyun Gayea,
Jeong Mun Seok,
Jeon Seokwoo
Publication year - 2019
Publication title -
advanced sustainable systems
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.499
H-Index - 24
ISSN - 2366-7486
DOI - 10.1002/adsu.201900084
Subject(s) - heterojunction , photocatalysis , materials science , quantum dot , graphene , visible spectrum , nanotechnology , absorption (acoustics) , charge carrier , optoelectronics , nanocomposite , band gap , chemical engineering , catalysis , chemistry , composite material , biochemistry , engineering
As rapidly growing environmental pollution demands the development of efficient photocatalytic materials, tremendous attention has been drawn to TiO 2 , a widely used photocatalytic material with cost‐effectiveness, stability, and outstanding reactivity. To maximize its photocatalytic efficiency by enhancing the photogenerated charge separation, lowering the intrinsically large bandgap (3.2 eV) of TiO 2 is a key problem to be overcome. Herein, a new design is reported for an efficient photocatalyst realized by heterostructuring a 3D nanostructured TiO 2 monolith (3D TiO 2 ) and graphene quantum dots (GQDs) through using 3‐aminopropyltriethoxysilane (APTES) as a linker. The incorporation of APTES between the TiO 2 /GQD interface enables the formation of a charge injection‐type heterostructure, as confirmed by transient absorption spectroscopy, providing improvement of both visible absorption and charge separation. As a result, the heterostructure exhibits a 242% enhanced photocatalytic performance compared to that of nonheterostructured 3D TiO 2 under visible irradiation, demonstrating its promising potential for practical photocatalytic applications in environmental remediation.

This content is not available in your region!

Continue researching here.

Having issues? You can contact us here