2022
DOI: 10.1016/j.chemosphere.2022.135937
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Zinc iron selenide nanoflowers anchored g-C3N4 as advanced catalyst for photocatalytic water splitting and dye degradation

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Cited by 22 publications
(9 citation statements)
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“…Yue et al found that the average H 2 evolution rate in the case of using 0.5% Pt/10% Zn/g-C 3 N 4 (0.2 g) was significantly increased, up to 59.5 μmol/h compared to 5.5 μmol/h of pure g-C 3 N 4 . This is due to the ability to capture electrons of Zn from the conductive band of g-C 3 N4, leading to enhanced separation of photogenerated electron–hole pairs and an increase in H 2 evolution. , More charge carriers were produced for water splitting because of increased optical absorption upon doping Zn. , The increase in the absorption intensity upon Zn-modification indicated a strong interaction between Zn and the matrix of g-C 3 N 4 which arose from the d–p repulsion between 3d and 2p orbitals of Zn and N, respectively . In a study of Ding et al, they also reported a simple treatment under high temperature (at 600 °C) to obtain alkali metal (including K, Li, or Na)-doped g-C 3 N 4 .…”
Section: Photocatalyst Characteristicsmentioning
confidence: 99%
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“…Yue et al found that the average H 2 evolution rate in the case of using 0.5% Pt/10% Zn/g-C 3 N 4 (0.2 g) was significantly increased, up to 59.5 μmol/h compared to 5.5 μmol/h of pure g-C 3 N 4 . This is due to the ability to capture electrons of Zn from the conductive band of g-C 3 N4, leading to enhanced separation of photogenerated electron–hole pairs and an increase in H 2 evolution. , More charge carriers were produced for water splitting because of increased optical absorption upon doping Zn. , The increase in the absorption intensity upon Zn-modification indicated a strong interaction between Zn and the matrix of g-C 3 N 4 which arose from the d–p repulsion between 3d and 2p orbitals of Zn and N, respectively . In a study of Ding et al, they also reported a simple treatment under high temperature (at 600 °C) to obtain alkali metal (including K, Li, or Na)-doped g-C 3 N 4 .…”
Section: Photocatalyst Characteristicsmentioning
confidence: 99%
“…This is due to the ability to capture electrons of Zn from the conductive band of g-C 3 N4, leading to enhanced separation of photogenerated electron−hole pairs and an increase in H 2 evolution. 212,213 More charge carriers were produced for water splitting because of increased optical absorption upon doping Zn. 214,215 The increase in the absorption intensity upon Znmodification indicated a strong interaction between Zn and the matrix of g-C 3 N 4 which arose from the d−p repulsion between 3d and 2p orbitals of Zn and N, respectively.…”
Section: ■ Photocatalyst Characteristicsmentioning
confidence: 99%
“…The higher photocurrent density seems attributed to the smaller bandgap of Nb 2 O 5 /PdS and efficient light absorption. [31,32] The efficient interfacial charge transfer between Nb 2 O 5 and PdS particles can also enhance the photocurrent response. The photocurrent response results imply that the Nb 2 O 5 /PdS heterostructure would be the most efficient photocatalyst compared to the other two materials owing to more light absorption and effective charge separation.…”
Section: Photocurrent Measurementsmentioning
confidence: 99%
“…The best performance of the composite is well explained by optical, electrochemical and structural property supported from UV-Vis DRS, EIS, photocurrent response, and BET surface area. [32]…”
Section: Photocatalytic Water Splittingmentioning
confidence: 99%
“…Subsequently, numerous research efforts involving a multitude of semiconductors have been aimed at photocatalytic water splitting. The overall water splitting mechanism proceeds as follows: the photocatalyst upon absorbing photonic energy greater than its band gap energy generates bulk electron–hole pairs that migrate to the surface without recombination to facilitate reduction and oxidation of water, respectively, to yield H 2 and O 2 . For photocatalytic water splitting, the bottom of the conduction band must be higher than the reduction potential of H + to H 2 (0 V vs NHE) and the top of the valence band must be lower than the oxidation potential (1.23 V vs NHE) . In addition, crossing the activation barrier in the charge transfer process requires photonic energy greater than the photocatalyst band gap for efficient water splitting .…”
Section: Introductionmentioning
confidence: 99%