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Cited by 200

The DOI matches its Crossref record; 1 of the 1 references it cites were found in a registry or an index.

g-C3N4/TiO2 Mesocrystals Composite for H2 Evolution under Visible-Light Irradiation and Its Charge Carrier Dynamics

Elbanna, Ossama, Fujitsuka, Mamoru, Majima, Tetsuro·2017·ACS Applied Materials & Interfaces

Abstract

The photocatalytic performance of graphitic carbon nitride (g-C 3 N 4 ) has been limited to low efficiency due to fast charge recombination. Here, we constructed g-C 3 N 4 nanosheets/TiO 2 mesocrystals metal-free composite (g-C 3 N 4 NS/TMC) to promote the efficiency of charge separation. The photocatalytic H 2 evolution experiments indicate that coupling g-C 3 N 4 NS with TMC increases photogenerated charge carriers in g-C 3 N 4 NS/TMC composite due to efficient charge separation. g-C 3 N 4 NS (31 wt %)/TMC shows the highest photocatalytic activity and the corresponding H 2 evolution rate is 3.6 μ mol h –1 . This value is 20 times larger than that of g-C 3 N 4 NS without any noble metal cocatalyst under visible-light irradiation (λ > 420 nm). The photocatalytic activity of g-C 3 N 4 NS/TMC (3.6 μmol h –1 ) is 7 times higher than that of g-C 3 N 4 NS/P25 (0.5 μ mol h –1 ), confirming the importance of strong interface interaction between two-dimensional g-C 3 N 4 NS and plate-shape TMC. Femtosecond time-resolved diffuse reflectance (fs-TDR) was employed to study the fundamental photophysical processes of bulk g-C 3 N 4, g-C 3 N 4 NS, and g-C 3 N 4 /TMC composite which are essential to explain the photocatalytic activity. Using fs-TDR, we demonstrate that the photocatalytic activity depends on the increased driving force for photoinduced electron transfer and a higher percentage of photogenerated charges.

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Metadata

Authors
Elbanna, O., Fujitsuka, M., & Majima, T.
Venue
ACS Applied Materials & Interfaces
Published
2017-09-27
Volume
9
Issue
40
Pages
34844-34854
ISSN
  • 1944-8244 (ISSN-L)
  • 1944-8252
OpenAlex
W2754511527
Cited by
200
References
1
FWCI
5.91
Type
journal article
Language
en
Open access
closed

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