2019
DOI: 10.1039/c8na00372f
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Unraveling the impact of the Pd nanoparticle@BiVO4/S-CN heterostructure on the photo-physical & opto-electronic properties for enhanced catalytic activity in water splitting and one-pot three-step tandem reaction

Abstract: Influence of Pd NPs in the BiVO4/S-CN photocatalyst is demonstrated for the efficient water splitting and imine synthesis via tandem reaction.

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Cited by 15 publications
(12 citation statements)
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References 78 publications
(114 reference statements)
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“…47 To estimate the band edge locations of Zn@MA-POP, a Mott−Schottky analysis was performed (Figure 4d), which showed a positive slope of 1/C 2 vs applied potential, characteristic of an n-type semiconductor. 48 The flat band potential of Zn@MA-POP calculated from the x intercept is −1.05 V. 49 For n-type semiconductors, the conduction band edge potential is defined as a drop in the flat band potential by 0.10 V, and hence the calculated CB/LUMO potential is −0.95 V. Further, the VB/HOMO position was found to be 1.55 V using the equation E VB − E CB = E g . 50 The HOMO and LUMO distributions from a DFT analysis of the Zn@MA-POP unit (Figure 4e) along with the band alignment show that the HOMO is mainly localized on the TPH moiety, whereas the LUMO is delocalized across the Zn-core unit, which basically acts as an electron acceptor.…”
Section: ■ Results and Discussionmentioning
confidence: 99%
“…47 To estimate the band edge locations of Zn@MA-POP, a Mott−Schottky analysis was performed (Figure 4d), which showed a positive slope of 1/C 2 vs applied potential, characteristic of an n-type semiconductor. 48 The flat band potential of Zn@MA-POP calculated from the x intercept is −1.05 V. 49 For n-type semiconductors, the conduction band edge potential is defined as a drop in the flat band potential by 0.10 V, and hence the calculated CB/LUMO potential is −0.95 V. Further, the VB/HOMO position was found to be 1.55 V using the equation E VB − E CB = E g . 50 The HOMO and LUMO distributions from a DFT analysis of the Zn@MA-POP unit (Figure 4e) along with the band alignment show that the HOMO is mainly localized on the TPH moiety, whereas the LUMO is delocalized across the Zn-core unit, which basically acts as an electron acceptor.…”
Section: ■ Results and Discussionmentioning
confidence: 99%
“…A reduction in the flat band potential by −0.10 V is considered as the conduction band edge potential for n-type semiconductors. 64 The calculated CB potentials from Mott−Schottky analysis using flat band potentials for g-CN, Zr-Thia(50)/g-CN, Zr-Thia(75)/g-CN, and Zr-Thia(100)/g-CN are calculated to be −0.88 V, −0.89 V, −1.0 V, and −0.92 V, respectively. The bandgap obtained from UV−visible spectroscopy, VBXPS derived valence band potential, and conduction band potential evaluated from M-S analysis gives the plausible band edge structure against the standard potential of Ag/AgCl.…”
Section: ■ Results and Discussionmentioning
confidence: 99%
“…The flat band potentials for g-CN, Zr-Thia(50)/g-CN, Zr-Thia(75)/g-CN, and Zr-Thia(100)/g-CN calculated from x -intercept are −0.98 V, −0.99 V, −1.10 V, and −1.02 V, respectively. A reduction in the flat band potential by −0.10 V is considered as the conduction band edge potential for n-type semiconductors . The calculated CB potentials from Mott–Schottky analysis using flat band potentials for g-CN, Zr-Thia(50)/g-CN, Zr-Thia(75)/g-CN, and Zr-Thia(100)/g-CN are calculated to be −0.88 V, −0.89 V, −1.0 V, and −0.92 V, respectively.…”
Section: Resultsmentioning
confidence: 99%
“…Several catalysts have been reported for the simultaneous photocatalytic oxidation of alcohols by photogenerated holes and reduction of nitrobenzene to aniline by photogenerated electrons. [30][31][32][33][34][35] TiO 2 , C 3 N 4 , BiVO 4 , and CdS based composite catalysts have been employed for this purpose. [30][31][32][33][34][35] Most of these catalysts were fabricated by a multi-step synthesis protocol.…”
Section: Introductionmentioning
confidence: 99%
“…[30][31][32][33][34][35] TiO 2 , C 3 N 4 , BiVO 4 , and CdS based composite catalysts have been employed for this purpose. [30][31][32][33][34][35] Most of these catalysts were fabricated by a multi-step synthesis protocol. The direct one-pot synthesis of secondary amines by the reaction of nitroarenes and alcohols is somewhat tricky, and therefore only a handful of reports are available.…”
Section: Introductionmentioning
confidence: 99%