2D/2D heterojunction of Ti 3 C 2 /g-C 3 N 4 nanosheets for enhanced photocatalytic hydrogen evolution
Photocatalytic hydrogen evolution from water has received enormous attention due to its ability to address a number of global environmental and energy-related issues. Here, we synthesize 2D/2D Ti 3 C 2 /g-C 3 N 4 composites by electrostatic self-assembly technique and demonstrate their use as photoc...
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Published in | Nanoscale Vol. 11; no. 17; pp. 8138 - 8149 |
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Main Authors | , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
England
Royal Society of Chemistry (RSC)
25.04.2019
|
Online Access | Get full text |
ISSN | 2040-3364 2040-3372 |
DOI | 10.1039/C9NR00168A |
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Summary: | Photocatalytic hydrogen evolution from water has received enormous attention due to its ability to address a number of global environmental and energy-related issues. Here, we synthesize 2D/2D Ti
3
C
2
/g-C
3
N
4
composites by electrostatic self-assembly technique and demonstrate their use as photocatalysts for hydrogen evolution under visible light irradiation. The optimized Ti
3
C
2
/g-C
3
N
4
composite exhibited a 10 times higher photocatalytic hydrogen evolution performance (72.3 μmol h
−1
g
cat
−1
) than that of pristine g-C
3
N
4
(7.1 μmol h
−1
g
cat
−1
). Such enhanced photocatalytic performance was due to the formation of 2D/2D heterojunctions in the Ti
3
C
2
/g-C
3
N
4
composites. The intimate contact between the monolayer Ti
3
C
2
and g-C
3
N
4
nanosheets promotes the separation of photogenerated charge carriers at the Ti
3
C
2
/g-C
3
N
4
interface. Furthermore, the ultrahigh conductivity of Ti
3
C
2
and the Schottky junction formed between g-C
3
N
4
/MXene interfaces facilitate the photoinduced electron transfer and suppress the recombination with photogenerated holes. This work demonstrates that the 2D/2D Ti
3
C
2
/g-C
3
N
4
composites are promising photocatalysts thanks to the ultrathin MXenes as efficient co-catalysts for photocatalytic hydrogen production. |
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Bibliography: | USDOE |
ISSN: | 2040-3364 2040-3372 |
DOI: | 10.1039/C9NR00168A |