2015
DOI: 10.1016/j.solmat.2015.01.037
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Z-scheme SnO2−x/g-C3N4 composite as an efficient photocatalyst for dye degradation and photocatalytic CO2 reduction

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Cited by 383 publications
(157 citation statements)
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“…Therefore, potential of the photoinduced electron-hole pairs and the absorbed light can be fully utilized. For example, He et al reported SnO 2-x /g-C 3 N 4 composite as an efficient Z-scheme photocatalytic system [63]. By carrying out a series of radicals-trapping experiments, it was found that a Z-scheme photocatalytic system of SnO 2-x /g-C 3 N 4 was successfully created instead of conventional heterojunction-type photocatalytic system.…”
Section: Figmentioning
confidence: 99%
“…Therefore, potential of the photoinduced electron-hole pairs and the absorbed light can be fully utilized. For example, He et al reported SnO 2-x /g-C 3 N 4 composite as an efficient Z-scheme photocatalytic system [63]. By carrying out a series of radicals-trapping experiments, it was found that a Z-scheme photocatalytic system of SnO 2-x /g-C 3 N 4 was successfully created instead of conventional heterojunction-type photocatalytic system.…”
Section: Figmentioning
confidence: 99%
“…In the Z-scheme mechanism, the scavenging studies has been reported for various direct Z-scheme photocatalysts such as g-C 3 N 4 /TiO 2 , NaNbO 3 /WO 3 , WO 3 /g-C 3 N 4 , BiOCl/g-C 3 N 4 , Bi 2 O 3 /g-C 3 N 4 , Bi 2 O 3 /NaNbO 3 , BiVO 4 /g-C 3 N 4 , Ag 3 PO 4 /g-C 3 N 4 , SnO 2-x /g-C 3 N 4 and α-Fe 2 O 3 /Cu 2 O. [55][56][57][58][59][60][61][62][63][64] The PL analysis results further support the superior photocatalytic efficiency of the direct Z-scheme CIS/TNP photocatalysts (Figure 9). At 330 nm excitation (Figure 9), the PL intensities of the x%-CIS/TNP composites are lower than that of TNP indicating slower recombination rates.…”
Section: Photocatalytic Mechanismmentioning
confidence: 99%
“…In heterojunction the accumulated holes in the valence band (VB) of CN cannot oxidize the surface hydroxyl (-OH) groups to hydroxyl radicals ( • OH), because the VB position of CN has a lower positive potential (+1.575 eV) than that required for the oxidation of -OH groups (-OH/ • OH = +2.4 eV). To surmount this, development of Z-scheme based photocatalysts has aroused increased attention due to its efficient separation of photogenerated electron-hole pairs in two different semiconductors [21][22][23][24][25]. Yu et al [26] revealed a direct Z-scheme-based photocatalytic mechanism in CN/TiO 2 photocatalysts.…”
Section: Introductionmentioning
confidence: 99%