N-doped rutile TiO 2 nanorod@g-C 3 N 4 core/shell S-scheme heterojunctions for boosting CO 2 photoreduction activity
The design of heterojunction photocatalysts is regarded as a very effective method to solve the high recombination rate of photogenerated charge carriers for CO 2 photoreduction into hydrocarbons, and interface engineering is urgently required to achieve high efficiency. Herein, graphitic carbon nit...
Saved in:
Published in | Catalysis science & technology Vol. 13; no. 3; pp. 898 - 909 |
---|---|
Main Authors | , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
06.02.2023
|
Online Access | Get full text |
Cover
Loading…
Summary: | The design of heterojunction photocatalysts is regarded as a very effective method to solve the high recombination rate of photogenerated charge carriers for CO
2
photoreduction into hydrocarbons, and interface engineering is urgently required to achieve high efficiency. Herein, graphitic carbon nitride (g-C
3
N
4
, CN) was uniformly grown on the surface of nitrogen-doped rutile TiO
2
(NT) nanorods by
in situ
deposition, and a NT@CN core/shell step-scheme (S-scheme) heterojunction system composed of NT nanorods and g-C
3
N
4
was synthesised. The as-synthesised heterojunction containing 55 wt% g-C
3
N
4
delivered the highest CO
2
photoreduction activity (33.35 μmol g
−1
for CO) without additional cocatalysts or external sacrificial agents, which was 7.1 times higher than that of bare NT nanorods. This improved CO
2
reduction activity was attributable to the large surface area and impactful S-scheme heterostructure, which imparted the catalyst with sufficient visible-light harvesting ability, promoted the segregation and transformation of the photoinduced charge pairs, and enhanced the redox ability of the carriers. Concurrently, the NT@CN photocatalyst exhibited excellent reusability and stability. This work offers a new basis for designing and preparing rutile TiO
2
-based S-scheme heterojunctions with enhanced CO
2
reduction performance. |
---|---|
ISSN: | 2044-4753 2044-4761 |
DOI: | 10.1039/D2CY01839J |